The Brain and Mental Health Benefits of Low-Level Laser Therapy (LLLT) & Photobiomodulation

Low-level laser/light therapy (LLLT) is an important treatment that I have used over the years to support my brain after serious concussions, toxic mold exposure and multiple psychiatric prescriptions

And in my experience, it is one of the most efficient ways to boost brain function and improve mental health. 

Yet your doctor likely has no idea what it is. 

It’s about as cutting-edge as it gets, and even more unconventional than neurofeedback. But it works. 

Also known as photobiomodulation, LLLT is the application of low-power lasers or light-emitting diodes (LEDs) to the body for therapeutic purposes.  When LLLT is applied to the brain, it is known as transcranial LLLT or transcranial photobiomodulation (44). 

LLLT has been around since 1967, and there are now more than four thousand scientific studies showing that it can help treat a variety of disorders without any harmful effects. Unlike high-intensity surgical lasers, low-powered lasers do not cut or burn tissue. Instead, these lasers stimulate a biological response and encourage cells to function properly (11, 12, 33). 

And luckily, it’s very easy to treat yourself at home with LLLT using red and infrared light.

I have used three main devices on my brain. They significantly improved the quality of my life over the years.

Make sure you read the Recommended Devices section below, where I discuss the different devices I have used. 

Picture of mitochondria being irradiated and stimulated by red and infrared light.

How It Works

Research shows that red and infrared light between the wavelengths of 632 nanometers (nm) and 1064 nm produce positive biological effects. For brain cells, the optimal range appears to be between 800 nm and 1000 nm, as these wavelengths can penetrate the scalp and skull and reach the brain (19, 20, 25-31).

The devices I have used fall within this range. 

The light emitted from the devices below stimulate a photochemical reaction within cells, which can accelerate the natural healing process and cause beneficial changes in behaviour (45).

How does it do this?

Mainly by supporting your mitochondria

As I’ve discussed before, mitochondria are considered the “powerhouses of the cell,” generating most of the energy in your body in the form of adenosine-5’- triphosphate (ATP). 

ATP is your body’s main source of cellular fuel. You are constantly using it, and your brain needs enough of it to work properly. 

Proper mitochondrial function and ATP production is critical for neuroprotection, cognitive enhancement, and the prevention and alleviation of several neurological and mental disorders (46).

And research demonstrates that transcranial LLLT supports mitochondrial function and significantly increases the production of ATP in the brain (3-5, 8-10, 13-17, 21-22, 34, 45).

Your mitochondria contain photoacceptors that absorb the photons from light and convert them into ATP – energy that can be used to perform cellular tasks and biological processes (39, 40).

This process is comparable to plant photosynthesis, during which sunlight is absorbed by plants and converted to energy for the plants to grow (23, 24). 

By stimulating the mitochondria and producing more ATP, LLLT gives brain cells extra ATP energy to work better and heal and repair themselves.

On top of this, LLLT has also been shown to:

Click here to subscribe

My Experience and What You Should Expect

LLLT is one of the most impactful and helpful actions I took to optimize my brain and mental health.

Man using LLLT helmet and intranasal Vielight device.

By the time I was off all psychiatric medications, I had lost a lot of my full cognitive capabilities. Thankfully, LLLT helped restore them.

Here are some of the results I noticed:

  • Increased cognitive function

  • Sharper thinking

  • Improved mood, concentration, alertness

  • Less fatigue and reduced need for sleep

  • More mental motivation, endurance and productivity

Overall, it improved my mental constitution. I didn’t get as fatigued and worn down as easily and I could focus and think harder for longer periods of time.

LLLT also has a cumulative effect. Your brain becomes stronger and more resilient over time as you do the treatment consistently.  

It allowed me to reduce the number of supplements I was taking daily. I now realize that I needed the treatment for many years, but I just didn’t know it existed.

Luckily, I started treating myself on a regular basis and have never felt better. 

Many serious brain injuries and mental illnesses can be successfully treated with LLLT, including depression, anxiety, post-traumatic stress disorder, traumatic brain injury, post-concussion syndrome, stroke and Alzheimer's disease.

I explore how LLLT has been shown to help each of these disorders below. Feel free to skip to the disorder you're struggling with to learn more.

 

Depression and Anxiety

Studies in rats and humans provide evidence that LLLT improves mood and decreases depressive symptoms.

In 2009, researchers took 10 patients with a history of major depression and anxiety (including post-traumatic stress disorder and substance abuse) and applied LLLT to their foreheads for four weeks. At the end of the study, six of the 10 patients experienced a remission of their depression, and seven of the 10 patients experienced a remission of their anxiety. There were no observable side effects (54). 

The data supports that LLLT to the head constitutes a promising neurotherapeutic tool to modulate behaviour in a non-invasive manner.
— Dr. Julio C. Rojas, MD, PhD, University of California

This makes sense considering that several studies show that depression is linked to abnormal blood flow in the frontal cortex of the brain, and LLLT increases blood flow and circulation (47, 53). 

Other studies have shown that participants report a significant increase in positive emotions and a reduction in depressive symptoms for two weeks after LLLT treatment (55-57). 

Sufferers of traumatic brain injury (TBI) also experience a decrease in depression, anxiety, irritability and insomnia, and an overall improvement in quality of life, because of LLLT (58, 59).  

I personally experienced all of these results.

 

Traumatic Brain Injury

Traumatic brain injury (TBI) is a growing health concern. An estimated 1.7 million people sustain a TBI annually in the U.S. (60). 

Mild TBIs (concussions) make up 75 per cent of all brain injuries. Military personnel deployed to Iraq and Afghanistan frequently experience mild TBI while overseas, and many months after they return home, they often struggle with PTSD, depression and anxiety (61, 62). 

And research shows that transcranial LLLT can help (63). 

I personally experienced this. In 2010, I suffered multiple concussions while living in a moldy home, and thankfully LLLT helped me recover from post-concussion syndrome.

A number of human studies show that patients with chronic mild TBI experience improved cognition, memory and sleep with LLLT treatment. 

One study examined whether LLLT could help 11 patients with chronic mild TBI symptoms. They all had cognitive dysfunction, and four of them had multiple concussions like I did. 

After 18 LLLT sessions, their cognition, memory and verbal learning improved. Participants also said they slept better and had fewer PTSD symptoms. Coworkers, friends and family reported improved social, interpersonal, and occupational functioning (65). 

If LLLT was a drug, we would definitely be hearing about it.

In another study, 10 people with chronic TBI were given 10 treatments of LLLT (810 nm) and witnessed a reduction in headaches, cognitive dysfunction, sleep problems, anxiety, depression and irritability (66). 

There have also been a few case studies showing beneficial effects of transcranial LLLT in TBI patients (67, 68):

Seven years after closed-head TBI from a motor vehicle accident, case 1 (a 66-year-old woman) began transcranial LED treatments. Before LLLT treatment, she could focus on her computer for only 20 minutes. After eight weekly LLLT treatments, her focused computer time increased to 3 hours. She has treated herself nightly at home for 5.5 years now and maintains her improved cognition at age 72 years.
Case 2 (a 52-year-old retired, high-ranking female military officer) had a history of multiple closed-head injuries. Before beginning LLLT treatments, she was on medical disability for 5 months. After 4 months of nightly LLLT treatments at home, she returned to working full-time as an executive consultant with an international technology consulting firm and discontinued medical disability. Neuropsychological testing performed after 9 months of transcranial LED showed significant improvement in cognition and memory, as well as reduction in post-traumatic stress disorder symptoms.
Case 3 received 20 LLLT treatments over two months and experienced highly favourable outcomes with decreased depression, anxiety, headache, and insomnia, whereas cognition and quality of life improved.

So LLLT can improve cognition, reduce costs in TBI treatment and be applied at home?

Hmm, sounds like something the pharmaceutical industry would not like people to know about – and something that would force them to lose a lot of life-long customers. 

Several mouse studies also show that transcranial LLLT can prevent cell death and increase neurological performance after TBI (69-72). 

Researchers believe that LLLT works so well for people struggling with TBI symptoms because mitochondria in the brain are significantly dysfunctional after TBI, resulting in an inadequate supply of ATP, and LLLT can support the mitochondria and increase ATP production (73-75, 79). 

There is also poor blood flow and oxygenation, and increased inflammation and oxidative stress in the brain after head injuries. This contributes to brain damage, but LLLT can help combat these problems, increase antioxidants, promote neurogenesis and relieve chronic symptoms (76-78, 80-83).

Click here to subscribe

Alzheimer's Disease and Cognitive Impairment

Research shows that LLLT can boost performance and improve cognitive function, including attention and memory, in elderly people, young healthy people and animals.  

Preliminary studies demonstrate that LLLT could slow down the progression of Alzheimer’s disease by decreasing a protein in the brain that is linked to dementia (84-86, 94). 

Downregulation of brain-derived neurotrophic factor (BDNF) occurs early in the progression of Alzheimer's disease, and LLLT has been shown to prevent brain cell loss by upregulating BDNF (87). 

LLLT could be used as a preventive intervention in people who present risk factors for Alzheimer’s disease, mild cognitive impairment, or a history of head trauma. In such patients, LLLT could be combined with cognitive intervention approaches.
— Dr. Francisco Gonzalez-Lima, PhD, University of Austin, Texas

Researchers have also applied LLLT to middle-aged mice, and discovered that the memory and cognitive performance of the middle-aged mice improved so much that it was comparable with that of young mice. The researchers concluded that LLLT should be “applied in cases of general cognitive impairment in elderly persons” (5, 88). 

Several others studies have shown that LLLT significantly increases alertness, awareness and sustained attention, and improves short-term memory and reaction time. Study participants also made fewer errors during tasks and tests (89-91, 93, 95). 

Another study found that LLLT was just as effective as exercise at enhancing cognition, likely by providing neuroprotection and supporting the mitochondria (92, 96).

 

Stroke

Multiple studies show that LLLT can significantly reduce brain damage and improve recovery outcomes after a stroke (110-113). 

In one study, researchers applied LLLT over the entire surface of the head of stroke patients approximately 18 hours after a stroke. Five days after the stroke, they found significantly greater improvements in the LLLT-treated group. The improvements continued 90 days after the stroke. At the end of the study, 70% of the patients treated with real LLLT had a successful outcome compared with only 51% of the control subjects (114). 

Follow up studies with over 600 stroke patients found similar beneficial results. Researchers believe increase in the production of ATP is responsible for the improvements (115, 116, 117).  

Numerous studies also show that LLLT significantly reduces neurological problems and improves behaviour in rats and rabbits after stroke. It also increases the growth of new brain cells in these animals, improving their overall recovery (118-124).

 

Other Disorders

There are a number of other disorders that can also improve with LLLT treatment: 

  • Parkinson’s disease (PD) – “Mitochondria in PD tissues are compromised, and LLLT could be developed as a novel treatment to improve neuronal function in patients with PD” (109).

  • Amyotrophic lateral sclerosis (ALS) - Mitochondrial dysfunction and oxidative stress play an important role in motor neuron loss in ALS. Motor function significantly improved with LLLT in a group of people in the early stage of the disease (99).

  • Autism – Linked to mitochondria dysfunction and inflammation, so LLLT would likely help (103, 104).

  • Bipolar disorder – Linked to mitochondria dysfunction and inflammation (105, 106, 107)

  • Schizophrenia – Linked to mitochondria dysfunction and inflammation (105, 106)

  • Smoking Cessation – Check out this video.

  • Alcoholism (101, 102)

  • Opiate addiction (102)

  • Headaches and migraines (108)

  • Acne - This is unrelated to brain health but LLLT can also treat acne. Improving my diet helped me overcome my acne many years ago, but I definitely wish I had known about LLLT when I had it. An integrative physician I know has had a lot of success with her patients struggling with acne and other skin issues (97, 98).

Recommended Devices

I first discovered LLLT when reading Dr. Norman Doidge’s book, The Brain's Way of Healing: Remarkable Discoveries and Recoveries from the Frontiers of Neuroplasticity.

Dr. Doidge talks about the BioFlex Laser Therapy equipment, which costs tens of thousands of dollars.

I found an integrative physician who owned a Bioflex and I gave it a try. 

After a few sessions, I started experiencing beneficial effects.

So I decided to go ahead and buy my own LLLT devices for much cheaper.

I ended up finding and trying a number of different LLLT devices myself

They were much less expensive than the Bioflex, and I wanted to see how they compared to the Bioflex.

Many of the devices I bought didn't help me very much because they weren't powerful enough.

Most light devices aren't very effective at penetrating the skull.

But after a lot of research, and trial and error, I found devices that were powerful enough.

And they did help me.

And they provided me with the same brain and mental health benefits as the expensive Bioflex.

Here are the three devices I now recommend because they actually work:

  • Optimal 1000 Brain Photobiomodulation Therapy Light (Combo Red/NIR) - This is a powerful device that shines 660 nm of red light and 850 nm of infrared light. Like I have, you can shine it on your forehead for 5 minutes every day. You can also shine it on other parts of your head and on your entire body, including on your thyroid, thymus gland and gut. I have experienced incredible benefits from doing this.

  • Optimal 300 Brain Photobiomodulation Therapy Light (Combo Red/NIR) - This is a smaller and more convenient device that I have taken with me when travelling.

  • Vielight Neuro Duo – This is a transcranial-intranasal headset with 810 nm of near infrared light. It penetrates deeper into brain tissue and is absorbed better by the central nervous system. If you decide to get this one, you can use the coupon code JORDANFALLIS for a 10% discount. Some research has shown a 20-fold higher efficiency of light delivery to the deep brain through the nose instead of transcranial application (125). Vielight has several different devices and you can also use the coupon code JORDANFALLIS for 10% off any of them.

Unlike most pharmaceuticals, LLLT is very safe, non-toxic and non-invasive, so you can easily try it on yourself without concern and see if it helps you like it has helped me (33, 34, 126). 

You can shine the light all over your head. But start slow and apply the light to different areas of your head for just 1-2 minutes, maybe even less if you’re really sensitive. Then work your way up to longer periods of time, perhaps 5-10 minutes per area. There’s no exact proper way to do this. Listen to your body and see how it affects you. 

It’s important to note that some people experience grogginess and fatigue after using LLLT. I experienced this the day after my first treatment. I was incredibly tired and lethargic. This was a sign that I did too much. 

If you feel extremely tired immediately after LLLT or the next day, take a break and do less next time. For example, if you applied light to your forehead for 3 minutes, then drop back down to 2 minutes for your next session. 

It is also important to cycle LLLT. The way it works is similar to exercise, so you need to take breaks in order to heal and get stronger. Using it everyday can cause a burnout effect. You can use it every other day to give your brain a chance to recover.

 

More Details on How I’ve Used the Optimal 1000 Therapy Light

Someone recently asked me for more details on how to use the Optimal 1000 Brain Photobiomodulation Therapy Light (Combo Red/NIR). So I thought I’d share what I told them here:

I usually hang the Optimal 1000 Brain Photobiomodulation Therapy Light (Combo Red/NIR) on my door, and then start by standing in front of it for about 10 minutes. I would say I'm about 1 or 2 feet away so that the light is shining on most of my body. I tend to prioritize my upper body though, particularly my thyroid, gut, thymus gland, and of course my head. But what I've found is that shining it on other parts of your body (besides my brain) actually leads to indirect cognitive benefits as well. So it's not just shining it on the brain that helps with cognitive function.

I will also sometimes turn my back to the light and shine it on my back and spine area, and on the back of my head, for about 5 to 10 minutes.

I also get much closer (perhaps about 2-3 inches away) and shine it just on my forehead for 4-5 minutes or so. It is safe to do this because our devices emit a very low, safe level of EMFs.

So what I usually do is 10 minutes on my entire body and then right after that, 5 minutes on my face/forehead. But it's completely fine to do them separately at different times of the day or on completely separate days if you want.

It's usually good to limit your exposure to a maximum of 20 minutes at a time though, because too much at one time can make you too tired and negate the beneficial effects.

The back of your head where your spine meets your skull is another great area to shine the light. I also like to shine the light on the sides of my head (around my ears) for a few minutes each.

 

Conclusion

Frankly, it’s ridiculous that this therapy is not more well-known and promoted by doctors. But like everything else on this website, you don’t have to wait for conventional medicine to catch up, and you can experiment with the LLLT devices yourself. There is a high benefit-to-risk ratio. 

I suspect that home-use application of LLLT will become much more popular in the coming years.

The remarkable effects of the treatment in healing the brain in a non-invasive manner, along with the fact that there is little evidence of any adverse side effects, suggests to me that it’s use will only increase.

At the same time, distrust in pharmaceuticals continues to grow because of uncertain efficacy and unbearable side effects. 

And as the Western population continues to age, the incidence of the degenerative brain diseases will only continue to increase, which will produce a severe financial and societal burden.

So people will realize they are at a disadvantage by not having their own device(s) and will start using them on a regular basis for optimal mental health and cognition.

 
Click here to subscribe

Live Optimally,

Jordan Fallis

Connect with me

References:

(1) http://www.ncbi.nlm.nih.gov/pubmed/23003120

(2) http://www.ncbi.nlm.nih.gov/pubmed/23281261

(3) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945284/

(4) http://www.ncbi.http://www.ncbi.nlm.nih.gov/pubmed/21274733lm.nih.gov/pubmed/21274733

(5) http://www.http://www.ncbi.nlm.nih.gov/pubmed/22850314.nlm.nih.gov/pubmed/22850314

(6) http://www.ncbi.nlm.nih.gov/pubmed/15954817

(7) http://onlinelibrary.wiley.com/doi/10.1002/lsm.20583/abstract

(8) http://www.ncbi.nlm.nih.gov/pubmed/9421973

(9) http://www.ncbi.nlm.nih.gov/pubmed/11959421

(10) http://www.ncbi.nlm.nih.gov/pubmed/17603858

(11) http://www.ncbi.nlm.nih.gov/pubmed/5098661  

(12) http://www.ncbi.nlm.nih.gov/pubmed/4659882

(13) http://www.ncbi.nlm.nih.gov/pubmed/10365442/

(14) http://www.ncbi.nlm.nih.gov/pubmed/6479342/ 

(15) http://www.ncbi.nlm.nih.gov/pubmed/2476986/

(16) http://www.ncbi.nlm.nih.gov/pubmed/17463313/

(17) http://www.ncbi.nlm.nih.gov/pubmed/19837048/

(18) http://www.ncbi.nlm.nih.gov/pubmed/19995444/

(19) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442599/

(20) http://www.sciencedirect.com/science/article/pii/S0004951414601276

(21) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288797/

(22) http://www.ncbi.nlm.nih.gov/pubmed/23239434?dopt=AbstractPlus

(23) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3953713/

(24) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065857/

(25) https://www.ncbi.nlm.nih.gov/pubmed/26535475

(26) https://www.ncbi.nlm.nih.gov/pubmed/26347062

(27) https://www.ncbi.nlm.nih.gov/pubmed/24568233

(28) https://www.ncbi.nlm.nih.gov/pubmed/21182447

(29) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796659/

(30) http://stroke.ahajournals.org/content/40/4/1359.long

(31) https://www.ncbi.nlm.nih.gov/pubmed/17463313

(32) http://www.medscape.com/viewarticle/775815

(33) https://www.psio.com/pdf/LLLT-of-eye-and-brain.pdf

(34) http://www.ncbi.nlm.nih.gov/pubmed/6200808

(35) http://www.ncbi.nlm.nih.gov/pubmed/22275301

(36) http://www.ncbi.nlm.nih.gov/pubmed/17439348

(37) http://www.ncbi.nlm.nih.gov/pubmed/17868110

(38) http://www.ncbi.nlm.nih.gov/pubmed/26202374

(39) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288797/

(40) http://www.isabelleverbeek.nl/wp-content/uploads/2014/05/A2-cognitie-Gonzalez-softlaser-fotonen-therapie-2014b.pdf

(41) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065857/

(42) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538543/

(43)https://www.researchgate.net/publication/273781132_Red_and_NIR_light_dosimetry_in_the_human_deep_brain

(44) http://www.ncbi.nlm.nih.gov/pubmed/25772014

(45) http://www.ncbi.nlm.nih.gov/pubmed/19837048

(46) http://www.sciencedirect.com/science/article/pii/S0006295213007417

(47) http://www.ncbi.nlm.nih.gov/pubmed/15025051

(48) http://www.ncbi.nlm.nih.gov/pubmed/16043128

(49) http://www.ncbi.nlm.nih.gov/pubmed/12946880

(50) http://www.ncbi.nlm.nih.gov/pubmed/15061044

(51) http://www.ncbi.nlm.nih.gov/pubmed/15570642

(52) http://www.ncbi.nlm.nih.gov/pubmed/12181629

(53) http://www.ncbi.nlm.nih.gov/pubmed/10739143

(54) http://www.ncbi.nlm.nih.gov/pubmed/19995444

(55) https://www.ncbi.nlm.nih.gov/pubmed/27267860

(56) http://dose-response.org/wp-content/uploads/2014/06/Gonzalez-Lima_2014.pdf

(57) https://www.ncbi.nlm.nih.gov/pubmed/23200785

(58) https://www.ncbi.nlm.nih.gov/pubmed/26535475

(59) https://www.ncbi.nlm.nih.gov/pubmed/26347062

(60) https://www.cdc.gov/traumaticbraininjury/pdf/bluebook_factsheet-a.pdf

(61) http://www.ncbi.nlm.nih.gov/pubmed/18234750/

(62) https://www.cdc.gov/traumaticbraininjury/pdf/mtbireport-a.pdf

(63) http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0053454

(65) https://www.ncbi.nlm.nih.gov/pubmed/24568233

(66) https://www.ncbi.nlm.nih.gov/pubmed/26347062

(67) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3104287/

(68) https://www.ncbi.nlm.nih.gov/pubmed/26535475

(69) http://www.ncbi.nlm.nih.gov/pubmed/17439348/

(70) http://www.ncbi.nlm.nih.gov/pubmed/19800810/

(71) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538543/

(72) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397203

(73) http://www.ncbi.nlm.nih.gov/pubmed/11059663

(74) http://www.ncbi.nlm.nih.gov/pubmed/19637966

(75) http://www.ncbi.nlm.nih.gov/pubmed/16120426

(76) http://www.ncbi.nlm.nih.gov/pubmed/18501200/

(77) http://www.ncbi.nlm.nih.gov/pubmed/19995444/

(78) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397203/

(79) http://www.ncbi.nlm.nih.gov/pubmed/17439348/

(80) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397203/

(81) http://www.ncbi.nlm.nih.gov/pubmed/17439348/

(82) http://www.ncbi.nlm.nih.gov/pubmed/17439348

(83)https://www.researchgate.net/publication/229161498_Transcranial_low_level_laser_light_therapy_for_traumatic_brain_injury

(84) http://www.ncbi.nlm.nih.gov/pubmed/18769048/

(85) https://www.researchgate.net/publication/263742704_Low-Level_Laser_Therapy_Ameliorates_Disease_Progression_in_a_Mouse_Model_of_Alzheimer%27s_Disease

(86) http://www.ncbi.nlm.nih.gov/pubmed/24994540

(87) http://www.ncbi.nlm.nih.gov/pubmed/23946409

(88) http://www.ncbi.nlm.nih.gov/pubmed/17855128/

(89) https://www.ncbi.nlm.nih.gov/pubmed/23200785

(90) https://www.ncbi.nlm.nih.gov/pubmed/27080072

(91) https://www.ncbi.nlm.nih.gov/pubmed/26017772

(92) https://www.ncbi.nlm.nih.gov/pubmed/27220529

(93) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3953713/

(94) http://www.ncbi.nlm.nih.gov/pubmed/24387311

(95) http://www.sciencedirect.com/science/article/pii/S1074742707001153

(96) http://www.ncbi.nlm.nih.gov/pubmed/23806754

(97) http://www.ncbi.nlm.nih.gov/pubmed/22615511

(98) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352636/

(99) http://www.ncbi.nlm.nih.gov/pubmed/19143012/

(100) https://www.ncbi.nlm.nih.gov/pubmed/26817446

(101) http://www.ncbi.nlm.nih.gov/pubmed/15674998/

(102) http://www.ncbi.nlm.nih.gov/pubmed/19995444

(103) http://www.ucdmc.ucdavis.edu/publish/news/newsroom/8932

(104) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554862/

(105) http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0004913

(106) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626880/

(107) http://www.ncbi.nlm.nih.gov/pubmed/23196997

(108) http://www.ncbi.nlm.nih.gov/pubmed/12811613

(109) http://www.ncbi.nlm.nih.gov/pubmed/19534794/

(110) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538543/

(111) http://www.ncbi.nlm.nih.gov/pubmed/19995444

(112) http://www.ncbi.nlm.nih.gov/pubmed/17463313/

(113) http://www.ncbi.nlm.nih.gov/pubmed/19233936/

(114) http://www.ncbi.nlm.nih.gov/pubmed/17463313/

(115) http://www.ncbi.nlm.nih.gov/pubmed/19233936/

(116) http://www.ncbi.nlm.nih.gov/pubmed/20425181/

(117) http://www.ncbi.nlm.nih.gov/pubmed/19837048/     

(118) http://www.ncbi.nlm.nih.gov/pubmed/19995444

(119) http://www.ncbi.nlm.nih.gov/pubmed/16946145/

(120) http://www.ncbi.nlm.nih.gov/pubmed/17693028/

(121) http://www.ncbi.nlm.nih.gov/pubmed/17678491/

(122) http://www.ncbi.nlm.nih.gov/pubmed/16444697/  

(123) http://www.ncbi.nlm.nih.gov/pubmed/17693028

(124) http://www.ncbi.nlm.nih.gov/pubmed/15155955

(125)https://www.researchgate.net/publication/273781132_Red_and_NIR_light_dosimetry_in_the_human_deep_brain

(126) http://www.ncbi.nlm.nih.gov/pubmed/23675984

Terms and Conditions

Privacy Policy

Affiliate Disclosure

Disclaimer

The Remarkable Antioxidant That Can Help Treat 6 Mental Illnesses

Silhouette of man, other person adding missing piece to puzzle.

When I went to the doctor years ago for help with my concussion symptoms and mental health challenges, he offered me two options – addictive sleeping pills or antidepressants.

That was it.

I was left in the dark.

I had no other options and nowhere to turn, so I had to take the medication.

Years later, I now know there are many other options and solutions.

N-acetyl-cysteine (NAC), a cheap amino acid and antioxidant, is an effective way to deal with the root cause of mental illness and sub-optimal cognition.

 

What's N-Acetylcysteine? How Can It Help The Brain?

N-acetyl-cysteine (NAC) is a modified form of the amino acid cysteine and helps your body produce glutathione.

Glutathione is a powerful antioxidant that supports liver detoxification and reduces free radicals in the body. 

Over the past 30 years, high doses of NAC have been used in emergency rooms to combat acetaminophen (Tylenol) toxicity (1, 2). 

But there is also an overwhelming amount of evidence showing that NAC can help treat a number of neurological and psychiatric disorders, and it helped me years ago when I was trying to recover from mental illness and post-concussion syndrome

A systematic review of all of the evidence suggests that NAC is effective at treating the following conditions (4, 6, 18, 19):

•    Major depressive disorder
•    Bipolar disorder
•    Drug addiction
•    Obsessive-compulsive disorder
•    Autism
•    Schizophrenia
•    Alzheimer's disease
•    Certain forms of epilepsy (progressive myoclonic)

NAC also reduces the severity of mild traumatic brain injury in soldiers, and animal studies show that it can improve cognition after moderate traumatic brain injury (5). 

Disorders such as anxiety and attention deficit hyperactivity disorder have preliminary evidence but require larger studies (4, 6). 

Overall, it’s clear to me that NAC should be a first-line treatment for mental illness.

My recommendation: I used to take 1200 mg of NAC every day to manage my long-term mental health. It was very helpful at one point in time. I no longer need to take it anymore because I’m completely recovered and well. It’s just not necessary for me anymore because I’m healthy. However, when I was taking it, I eventually started experienced some side effects due to heavy metal redistribution. Studies show that people benefit from taking anywhere between 500 mg to 3000 mg daily or every other day. But I find that many people actually do better when they take a lower dose because high doses of NAC can sometimes redistribute heavy metals into the brain. You’ll obviously want to avoid this. I now recommend people take just 250 mg of NAC, which can be found in the Optimal Antiox supplement. Optimal Antiox also contains a number of other antioxidants and nutrients that can support your brain and mental health. Optimal Antiox also includes leucine, which is an amino acid. Taking leucine with NAC prevents mercury from being reabsorbed into the central nervous system.

 

How Is It So Effective At Treating All These Mental Health Conditions?

First of all, it's important to note that NAC seems to target biological pathways that are common across all mental disorders.

Here are some possible explanations for its effectiveness:

  • NAC has anti-inflammatory properties, and inflammation has been linked to depression and other mental health disorders (12, 13).

  • NAC has also been shown to successfully cross the blood-brain-barrier and raise glutathione levels in the brain. Low levels of glutathione in the brain have been linked to a number of psychiatric disorders (8-11, 17-19, 24).

  • High levels of oxidative stress have been identified in the brains of patients with a variety of psychiatric illnesses. Increasing brain glutathione by supplementing with NAC can help reduce this oxidative stress and protect neurons from oxidative damage (20-23, 25).

  • Lastly, NAC may be having beneficial effects on patients by reducing glutamate, a major excitatory neurotransmitter in the brain that can lead to overstimulation (14-16, 26).

Therefore, if you take NAC, you're giving your body an efficient way to soak up excess glutamate. You’re also reducing oxidative stress and inflammation by giving it glutathione. As a result, this helps alleviate a number of different mental health problems. 

Below, I’ll lay out some of the research exploring NAC as a possible treatment for six mental health problems. Feel free to skip to your condition to learn about it. 

Click here to subscribe

Depression and Bipolar Disorder

Here is some of the research looking into NAC as a possible treatment for depression and bipolar disorder:

  • A randomized controlled trial examined 149 individuals with moderate depression. They received two grams of NAC or placebo. Before treatment, the estimated mean depression score was 19.7. At the end of the 8-week study, the score had decreased to 11.1. Individuals who received NAC witnessed improvements in functioning and quality of life (27).

  • Another randomized controlled trial looked at 75 patients with bipolar disorder. Two grams of NAC or placebo was given for 6 months. At the end of this period, the group who received NAC saw a reduction in their depression and significant improvements in their global, social and occupational functioning. The improvements were rated as “medium to high” and it was concluded that "NAC is a safe and effective augmentation strategy for depressive symptoms” (28).

  • Several other studies have examined the effects of NAC on bipolar disorder (including mania) and found that two grams of NAC daily significantly improves and even causes a full remission of both depressive and manic symptoms (29-31).

It’s important to note that some of these studies lasted 6 months, which is a very long time for randomized control trials. And all of the studies had beneficial effects and zero severe side effects. That’s quite impressive.

All of the above research makes sense in light of a meta-analysis that found that patients with bipolar disorder have significantly higher levels of oxidative stress and glutamate in their brain.

A number of mood-stabilizing medications aim to decrease glutamate, yet they come with numerous side effects (14-16, 26, 27, 32, 33).

And as I've discussed before, certain antidepressants can deplete glutathione, which further increases oxidative stress. 

 

Addiction

Substance abuse and addiction are very costly. Yet there are hardly any efficient treatments that prevent relapse. 

But a lot of research is emerging demonstrating a link between oxidative stress and drug addiction, and how NAC can help manage it (66-68). 

  • In a small study, 13 people abstaining from cocaine were given 2,400 mg of NAC or placebo over two days. The participants who received NAC witnessed a significant reduction in their withdrawal symptoms and cravings for cocaine (34). Follow-up studies also showed that NAC reduced desire and interest in cocaine (35, 36).

  • Smokers voluntarily reduce their cigarette use by around 25% after two weeks of supplementing with 2,400 mg of NAC (37, 65).

  • And it’s not just addiction to drugs. NAC also shows promise for the treatment of gambling addiction. A randomized control trial with 27 pathological gamblers showed that gamblers who supplemented with NAC scored 60% lower on the “Obsessive Compulsive Scale for Pathological Gambling." (38).

Here are 8 other nutrients that can help with addiction.

 

Obsessive-Compulsive Disorder (OCD)

Not surprisingly, there are brain similarities among people who suffer from addiction and obsessive–compulsive disorder (OCD).

Just like addiction, higher levels of oxidative stress and glutamate are found in people with OCD (39-44). 

The standard treatment for OCD is a combination of antidepressants and psychotherapy.

But around 20% of patients don’t get better with this combination, and many suffer from a variety of drug side effects (45). 

Since NAC is inexpensive and widely available, it’s clear that it has significant advantages for patients.

I also encourage you to check out this article for 21 other ways to treat OCD.

Click here to subscribe

Autism

Autism is a touchy subject. So let me start out by saying that NAC will not cure autism. Autism has many different causes and contributing factors.

However, NAC will likely improve some autistic symptoms. 

Multiple studies suggest that NAC is a well-tolerated treatment for autistic individuals and can reduce their irritability (46-48). 

Like the disorders above, research has found that autistic individuals have higher levels of oxidative stress and lower levels of the antioxidant glutathione in their brains, making it likely that NAC will help them (49-55). 

There is also lots of evidence suggesting that too much glutamate in the brain contributes to autistic symptoms. As discussed earlier, glutamate in a major excitatory neurotransmitter in the brain. It is also the precursor to GABA, a calming neurotransmitter that reduces anxiety

There is an enzyme that converts glutamate to GABA, and researchers have found that this enzyme is lower in individuals on the autism spectrum. This leads to more glutamate and less GABA, and therefore much more excitation. Not surprisingly then, glutamate antagonists (e.g. NAC) have been shown to reduce symptoms of autism, bringing them more into balance (56-60). 

Since oxidation and glutamate are abnormally elevated in persons with autism, NAC can kill two birds with one stone by providing an antioxidant effect and reducing glutamate levels in the brain of autistic individuals. 

 

Schizophrenia

The last mental disorder I’m going to explore is schizophrenia. There is a good amount of research suggesting that NAC can help with this condition as well.

  • Researchers gave 2 grams of NAC to schizophrenic patients during a six-month randomized control trial. The participants who received NAC experienced improvements in their symptoms, and many of them did not experience improvements from other treatments. They demonstrated improvements in insight, self-care, social interaction, motivation, and stabilization of mood. Follow-up studies found similar results (62, 63, 70).

  • I found one study that explored NAC’s ability to change schizophrenic patient’s electroencephalogram (EEG) synchronicity – a measure of electrical activity within the brain that I discussed in my post about neurofeedback (69).

  • I also found a case report of a young woman with treatment-resistant schizophrenia who showed significant improvements in symptoms by taking just 600 mg of NAC every day (64).

This makes sense considering there is an expanding body of evidence suggesting oxidative stress occurs in individuals with schizophrenia. Some research shows that the more oxidative stress a schizophrenic patient experiences, the worse their symptoms get. And several studies indicate that NAC may benefit schizophrenics by increasing glutathione and reducing glutamate (61, 71-74).

 

Conclusion

Overall, oxidation and glutamate are often abnormally elevated in people with a wide range of neurological and psychiatric disorders. 

NAC may correct these underlying problems by generating the antioxidant glutathione and reducing the excitatory neurotransmitter glutamate.

If you suffer from depression, bipolar disorder, OCD, drug addiction or autism, you could start taking it and see if it helps you. If it helps, keep taking. If not, then try something else. 

Many of the studies also suggest that NAC enhances the effectiveness of psychiatric medications. So if you're already on medication, NAC and your medication will likely work better together.

My recommendation: I used to take 1200 mg of NAC every day to manage my long-term mental health. It was very helpful at one point in time. I no longer need to take it anymore because I’m completely recovered and well. It’s just not necessary for me anymore because I’m healthy. However, when I was taking it, I eventually started experienced some side effects due to heavy metal redistribution. Studies show that people benefit from taking anywhere between 500 mg to 3000 mg daily or every other day. But I find that many people actually do better when they take a lower dose because high doses of NAC can sometimes redistribute heavy metals into the brain. You’ll obviously want to avoid this. I now recommend people take just 250 mg of NAC, which can be found in the Optimal Antiox supplement. Optimal Antiox also contains a number of other antioxidants and nutrients that can support your brain and mental health. Optimal Antiox also includes leucine, which is an amino acid. Taking leucine with NAC prevents mercury from being reabsorbed into the central nervous system.

 
Click here to subscribe

Live Optimally,

Jordan Fallis

Connect with me

References:

1.    http://www.ncbi.nlm.nih.gov/pubmed/677146/ 
2.    Atkuri, K.R., et al. “N-Acetylcysteine — a safe antidote for cysteine/glutathione deficiency”. Current Opinion in Pharmacology Vol. 7, No. 4 (2007): 355–359.
3.    http://www.ncbi.nlm.nih.gov/pubmed/16439183
4.    http://www.ncbi.nlm.nih.gov/pubmed/25957927
5.    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553161/ 
6.    http://www.ncbi.nlm.nih.gov/pubmed/11673605/ 
7.    http://www.ncbi.nlm.nih.gov/pubmed/12512991
8.    http://www.ncbi.nlm.nih.gov/pubmed/2029805/ 
9.    http://www.ncbi.nlm.nih.gov/pubmed/18004285/ 
10.    http://www.ncbi.nlm.nih.gov/pubmed/11691805  
11.    http://www.ncbi.nlm.nih.gov/pubmed/12603840
12.    http://www.ncbi.nlm.nih.gov/pubmed/20021321
13.    http://www.ncbi.nlm.nih.gov/pubmed/19122532
14.    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044191/ 
15.    http://www.ncbi.nlm.nih.gov/pubmed/17401648/ 
16.    http://www.ncbi.nlm.nih.gov/pubmed/12584726/ 
17.    http://www.ncbi.nlm.nih.gov/pubmed/12512991
18.    http://www.ncbi.nlm.nih.gov/pubmed/24752591  
19.    http://www.ncbi.nlm.nih.gov/pubmed/25004186
20.    Andreazza, A.C., et al. “Oxidative stress markers in bipolar disorder: a meta-analysis”. Journal of Affective Disorders Vol. 111, No. 2–3 (2008): 135–144. 
21.    Kim, H.K., et al. “Oxidation and nitration in dopaminergic areas of the prefrontal cortex from patients with bipolar disorder and schizophrenia”. Journal of Psychiatry & Neuroscience Vol. 39, No. 1 (2014): 130155.
22.    Wang, J.F., et al. “Increased oxidative stress in the anterior cingulate cortex of subjects with bipolar disorder and schizophrenia”. Bipolar Disorders Vol. 11, No. 5 (2009): 523–529.
23.    Gawryluk, J.W., et al. “Decreased levels of glutathione, the major brain antioxidant, in post-mortem prefrontal cortex from patients with psychiatric disorders”. The International Journal of Neuropsychopharmacology Vol. 14, No. 1 (2011): 123–130.
24.    Holmay, M.J., et al. “N-Acetylcysteine boosts brain and blood glutathione in Gaucher and Parkinson diseases”. Clinical Neuropharmacology Vol. 36, No. 4 (2013): 103–106.
25.    Gawryluk, J.W., et al. “Decreased levels of glutathione, the major brain antioxidant, in post-mortem prefrontal cortex from patients with psychiatric disorders”. The International Journal of Neuropsychopharmacology Vol. 14, No. 1 (2011): 123–130
26.    Gigante, A.D., et al. “Brain glutamate levels measured by magnetic resonance spectroscopy in patients with bipolar disorder: a meta-analysis”. Bipolar Disorders Vol. 14, No. 5 (2012): 478–487.
27.    Berk, M., et al. “The efficacy of N-acetylcysteine as an adjunctive treatment in bipolar depression: an open label trial”. Journal of Affective Disorders Vol. 135, No. 1–3 (2011): 389–394.
28.    http://www.ncbi.nlm.nih.gov/pubmed/18534556
29.    Magalhães, P.V., et al. “N-Acetylcysteine for major depressive episodes in bipolar disorder”. Revista Brasileira de Psiquiatria Vol. 33, No. 4 (2011): 374–378.
30.    Magalhães P.V., et al. “N-Acetyl cysteine add-on treatment for bipolar II disorder: a subgroup analysis of a randomized placebo-controlled trial. Journal of Affective Disorders Vol. 129, No. 1–3 (2011): 317–320.
31.    Magalhães, P.V., et al. “A preliminary investigation on the efficacy of N-acetyl cysteine for mania or hypomania”. The Australian and New Zealand Journal of Psychiatry Vol. 47, No. 6 (2013): 564–568.
32.     http://www.ncbi.nlm.nih.gov/pubmed/18539338/ 
33.    http://www.ncbi.nlm.nih.gov/pubmed/19568477/ 
34.    http://www.ncbi.nlm.nih.gov/pubmed/16449100/ 
35.    http://www.ncbi.nlm.nih.gov/pubmed/17606664/ 
36.    http://www.ncbi.nlm.nih.gov/pubmed/17113207/ 
37.    http://www.ncbi.nlm.nih.gov/pubmed/19103434
38.    http://www.ncbi.nlm.nih.gov/pubmed/17445781
39.    http://www.ncbi.nlm.nih.gov/pubmed/12207144
40.    http://www.ncbi.nlm.nih.gov/pubmed/19272303
41.    http://www.ncbi.nlm.nih.gov/pubmed/16682105
42.    http://www.ncbi.nlm.nih.gov/pubmed/18957313
43.    http://www.ncbi.nlm.nih.gov/pubmed/18006203
44.    http://link.springer.com/article/10.1007/s00213-005-0246-6
45.    http://www.ncbi.nlm.nih.gov/pubmed/19468281/ 
46.    http://www.ncbi.nlm.nih.gov/pubmed/23826003
47.    http://www.ncbi.nlm.nih.gov/pubmed/22342106
48.    http://www.ncbi.nlm.nih.gov/pubmed/23886027
49.    http://www.ncbi.nlm.nih.gov/pubmed/21519954
50.    http://www.ncbi.nlm.nih.gov/pubmed/22225920
51.    http://www.ncbi.nlm.nih.gov/pubmed/22127832
52.    http://www.ncbi.nlm.nih.gov/pubmed/16081262
53.    http://www.ncbi.nlm.nih.gov/pubmed/22528835
54.    http://www.ncbi.nlm.nih.gov/pubmed/21484198
55.    http://www.ncbi.nlm.nih.gov/pubmed/22051046
56.    http://www.ncbi.nlm.nih.gov/pubmed/21967199
57.    http://www.ncbi.nlm.nih.gov/pubmed/22653211
58.    http://www.ncbi.nlm.nih.gov/pubmed/17502791
59.    http://www.ncbi.nlm.nih.gov/pubmed/22342106
60.    http://www.ncbi.nlm.nih.gov/pubmed/22579303
61.    http://www.ncbi.nlm.nih.gov/pubmed/18538422/ 
62.    http://www.ncbi.nlm.nih.gov/pubmed/18436195/ 
63.    http://www.ncbi.nlm.nih.gov/pubmed/20868637/ 
64.    http://www.ncbi.nlm.nih.gov/pubmed/19735056/ 
65.    http://www.ncbi.nlm.nih.gov/pubmed/19103434/ 
66.    http://www.ncbi.nlm.nih.gov/pubmed/18440072
67.    http://www.ncbi.nlm.nih.gov/pubmed/18996163
68.    http://www.ncbi.nlm.nih.gov/pubmed/18225476
69.    Carmeli, C., et al. “Glutathione precursor N-acetyl-cysteine modulates EEG synchronization in schizophrenia patients: a double-blind, randomized, placebo-controlled trial”. PLoS One Vol. 7, No. 2 (2012): e29341.
70.    https://www.researchgate.net/publication/258347895_N-Acetylcysteine_as_an_Adjunct_to_Risperidone_for_Treatment_of_Negative_Symptoms_in_Patients_With_Chronic_Schizophrenia_A_Randomized_Double-Blind_Placebo-Controlled_Study
71.    http://www.ncbi.nlm.nih.gov/pubmed/19689277
72.    http://www.ncbi.nlm.nih.gov/pubmed/19576938
73.    http://www.ncbi.nlm.nih.gov/pubmed/19788631
74.    http://www.ncbi.nlm.nih.gov/pubmed/18205981

Terms and Conditions

Privacy Policy

Affiliate Disclosure

Disclaimer

How to Fight Alzheimer's Disease with Intranasal Insulin

A woman spraying insulin up her cose with an intranasal bottle.

Today I want to discuss "intranasal insulin", a cutting-edge therapy that could help a lot of people. 

Neurologists and psychiatrists tend to undervalue the impact of hormones originating outside the brain.

Until modern medicine treats the entire body as one unified system, people will continue to lose faith in conventional practitioners and look elsewhere for solutions to their chronic brain and mental health problems. 

As Dr. Suzanne Craft, Ph.D, Professor of Gerontology and Geriatric Medicine, explains:

People are now starting to understand the critical interaction between the brain and the body and that many of the peptides and hormones produced in the body have very substantial roles to play in the brain. I think we’re at the beginning of a very exciting era in which we’re going to be able to start putting together these systems to understand Alzheimer’s disease, which is clearly a disease of the entire organism, not just of the brain.

Insulin is one of the hormones that significantly affects brain function.

It's been shown to pass the blood-brain barrier and act on insulin receptors directly within the brain (3, 4). 

Not only does our body produce and release it, but it can also be taken as a medication, particularly for the treatment of diabetes (1, 2). 

Researchers have found that insulin has “neurotrophic, neuromodulatory, and neuroprotective effects” by:

Insulin in the dictionary.
In the brain, insulin has a number of roles to play. It promotes glucose uptake in the neurons of the hippocampal formation and the frontal lobes, areas that are involved in memory. Insulin also strengthens the synaptic connections between brain cells, helping to form new memories. In addition, insulin regulates the neurotransmitter acetylcholine, which plays an important role in learning and memory.
— Dr. Suzanne Craft, Ph.D

So, it clearly does a lot in the brain, and research shows that it can be therapeutic for a number of mental health conditions, particularly Alzheimer’s disease

In a new therapeutic approach, commercially-available insulin (Novalin R) is prepared and added to nasal spray bottles, and sprayed and inhaled through the nose to support brain and mental health. 

Dr. William Banks, Professor of Internal Medicine and Geriatrics, says there are more than 100 different intranasal compounds that are being tested for the treatment of Alzheimer’s disease

“Intranasal insulin” is just one of them, and it’s one of the more promising ones, as it’s been reported to significantly enhance memory, increase mental energy, reduce brain fog, improve mood, and lower anxiety and stress levels

Click here to subscribe

The Link Between Alzheimer’s Disease, Insulin and Diabetes

Many of the brain health experts I’ve talked to are convinced that Alzheimer’s disease should actually be called "Type 3 diabetes".

This is because diabetes and insulin are closely linked to cognitive decline and dementia

Many studies show that diabetes is associated with an increased risk of cognitive dysfunction, and people with diabetes are 2 to 3 times more likely to be diagnosed with Alzheimer’s disease and mild cognitive impairment than non-diabetics (14-21). 

Researchers have also found that insulin declines in the brain as people age, and patients with Alzheimer’s disease often have insulin resistance and reduced levels of insulin in their brains (25-30)

But what if insulin deficiency is detected in the brain, and then insulin is supplied to the brain, could neurodegeneration and the development of dementia be prevented? And could the progression of existing Alzheimer’s disease be halted?

The answers to these questions appears to be yes:

  • Diabetic patients who take insulin have improved memory and reduced rates of Alzheimer’s disease;

  • Elderly diabetics who take insulin have less severe Alzheimer’s disease compared with non-diabetics;

  • Insulin improves cognition and memory in people with Alzheimer’s disease; and

  • Insulin prevents and reverses brain degeneration and cognitive impairment in diabetic animals (22-24).

Check out the below video to learn more from one of the leading researchers in the field: 

Cutting-Edge Research Shows That Intranasal Insulin Improves Cognition and Memory

The intranasal route of insulin administration provides direct access to the cerebrospinal fluid and brain.

This allows insulin to directly enter the brain from the nose, and bind to receptors within specific areas of the brain that are involved in memory and cognition (42). 

Insulin receptors in the brain are found in high densities in the hippocampus, a region that is fundamentally involved in the acquisition, consolidation, and recollection of new information.

An increasing amount of research has been published over the last ten years, demonstrating that intranasal insulin can significantly improve cognition, attention, memory and overall brain function in people with mild cognitive impairment and Alzheimer’s disease (31-33, 38-39, 43-45). 

In fact, there are over 30 randomized, double-blind, placebo-controlled trials showing that it’s effective at improving memory, learning and cognitive performance in humans (34-37). 

Illustration of how intranasal insulin works.

Yet most people aren’t aware of it, and doctors aren’t prescribing it, while millions of people suffer from dementia

One study found that it improved objective biomarkers of neurodegeneration, including amyloid deposits and tau pathology, in people with Alzheimer’s disease within a few months. In the group of patients that didn’t receive intranasal insulin, brain function continued to deteriorate (40). 

In another study, researchers gave intranasal insulin to 104 adults with mild cognitive impairment or Alzheimer’s disease. At the end of the 4-month study, the participants who received insulin had significantly better memory and cognitive function compared to the group who didn’t receive insulin (41). 

The researchers also found that the improvements in cognition were correlated with improvements in objective biomarkers, and concluded that “intranasal insulin therapy can help to stabilize, slow, or possibly even reverse the course of Alzheimer’s disease (41). 

Because of the promising research so far, the US government is currently funding a two-year long clinical trial to see if intranasal insulin will help 240 people with Alzheimer’s disease. Results from the Study of Nasal Insulin in the Fight Against Forgetfulness (SNIFF) are expected to be released in 2017. 

And intranasal insulin doesn’t just help elderly people with dementia. It’s also been shown to improve memory in younger, healthy individuals (46-51). 

Click here to subscribe

Intranasal Insulin and Other Brain and Mental Health Disorders

Alzheimer’s disease isn’t the only brain and mental health condition that can benefit from intranasal insulin. 

Here are some others:

  • ADHD and drug addiction – Insulin affects dopamine, which is a neurotransmitter linked to both these conditions (52).

  • Depression, anxiety and anger – In one study, 38 healthy people took intranasal insulin for 8 weeks and experienced enhanced mood, increased self-confidence and reduced anger. Another study found that it affected heart-rate variability (53, 59).

  • Stroke – Researchers point out that “intranasally administered insulin possesses many of the ideal properties for acute stroke neuroprotection” (54, 62).

  • Bipolar disorder – One study found that intranasal insulin significantly improved executive function in patients with bipolar disorder (55).

  • Neurodevelopmental disorder – Two studies have found that intranasal insulin improves cognition, autonomy, motor activity, nonverbal communication, social skills and developmental functioning of children and adults with a rare neurodevelopmental disorder (Phelan-McDermid syndrome) (57, 58).

  • Overall brain function – “Intranasal insulin appears to restore complex neural networking in the direction of normalization”. In other words, it seems to “reboot” the brain (56).

  • Parkinson’s disease and Down Syndrome – There is no evidence for this yet but there are ongoing trials looking into whether intranasal insulin could help people with these conditions (60, 61).

 

Safety of Intranasal Insulin and How to Try It Yourself

Numerous studies show that intranasal insulin is incredibly safe and does not cause any significant adverse side effects. The only minor side effects I came across were dizziness, nose bleeding and mild rhinitis, but these were rare (63-65). 

This is because unlike regular insulin administration, intranasal insulin only affects the nose and brain. It doesn’t enter the bloodstream, change insulin levels throughout the entire body, or cause low blood sugar (66-83). 

Intranasal spray bottle.

Overall, I believe the benefits outweigh the risks and it’s worth trying, especially if you’re struggling with mild cognitive impairment or early Alzheimer’s disease. It may be another decade or more until the research trickles down and reaches your doctor’s office. Research shows that it takes about 17 years for new scientific evidence to be implemented in clinical practice

However, I’m not a doctor and you should definitely talk to your doctor about this if you’re considering trying it. If you have an open-minded doctor, perhaps they will support you in trying it. Don’t be surprised if they dismiss the idea entirely though. 

With that said, you can easily and legally buy insulin yourself. It’s available over the counter without a prescription at any pharmacy (in the US and Canada). Pharmacists hold it behind the counter and you just have to walk up and ask for “Novolin R.” In Canada, it’s called “Novolin Toronto.”

It’s that simple. You don’t need to provide personal identification or sign anything. It costs about $30.

After that, you can get a nasal spray bottle - like this one or this one

Then, use pliers to carefully remove the rubber cap from the insulin vial, and pour the insulin into the spray bottle. 

At this point, you’re ready to use it. Make sure to keep it in the fridge when you're not using it. 

Again, I’m not a doctor. So talk to your doctor about this before trying it. But I feel this is worth sharing and writing about considering it has massive potential to help many people who are struggling day-to-day. 

Click here to subscribe

Dosage

Each spray from the nasal bottle is 0.1mL or 10IU of insulin. 

Dosages in human studies range from 10IU to 160IU (1 to 16 sprays) daily. 

In the longest lasting study, participants took either 20 IU (2 sprays) or 40IU (4 sprays) of insulin daily for four months (86). 

So, if you’re going to try it, I wouldn’t take more than 40IU (4 sprays) for longer than 4 months.

However, participants in the ongoing SNIFF trial have been taking intranasal insulin for more than one year, so once the results from that study are released in 2017, my recommendation may change. 

Overall, self-experimentation is necessary to find the correct dosage that works best for you. 

 

Conclusion

Intranasal insulin is a very impressive and exciting substance, and the lack of side effects is encouraging. 

If you’re looking to improve your memory and brain function and avoid Alzheimer’s disease, it’s definitely worth considering and talking to your doctor about it. 

An elderly man sprays intranasal insulin up his nose.

All that’s needed is:

I’m aware that this might be little bit “out there” for some people, but I think it has the potential to help a lot of people reach optimal brain and mental health. 

Please share with anyone who is struggling with cognitive impairment or the early signs of dementia because it isn't a very well known treatment. 

 
Click here to subscribe

Live Optimally,

Jordan Fallis

Connect with me

References:

(1) http://link.springer.com/article/10.1007/s00125-003-1153-1

(2) http://diabetes.diabetesjournals.org/content/31/11/957.short

(3) http://press.endocrine.org/doi/abs/10.1210/edrv-13-3-387

(4) http://www.ncbi.nlm.nih.gov/pubmed/26401706

(5) https://www.ncbi.nlm.nih.gov/pubmed/15750214/

(6) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191295/

(7) https://www.ncbi.nlm.nih.gov/pubmed/15750214/

(8) https://www.ncbi.nlm.nih.gov/pubmed/22586589

(9) https://www.ncbi.nlm.nih.gov/pubmed/18348871

(10) https://www.ncbi.nlm.nih.gov/pubmed/23907764

(11) https://www.ncbi.nlm.nih.gov/pubmed/26040423

(12) https://www.ncbi.nlm.nih.gov/pubmed/26777890

(13) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391678/

(14) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191295/

(15) https://www.ncbi.nlm.nih.gov/pubmed/22201977/

(16) http://diabetes.diabetesjournals.org/content/54/5/1264?ijkey=3186b318b004c253abda2b3f67535508da9fa50a&keytype2=tf_ipsecsha

(17) http://diabetes.diabetesjournals.org/content/63/7/2253?ijkey=5cc5fc39ea0a601c551a668d0829247222ae292e&keytype2=tf_ipsecsha

(18) http://care.diabetesjournals.org/content/20/3/438

(19) https://www.ncbi.nlm.nih.gov/pubmed/11678970

(20) https://www.ncbi.nlm.nih.gov/pubmed/10647755

(21) http://www.alzheimersanddementia.com/article/S1552-5260(13)02918-X/abstract

(22) https://www.ncbi.nlm.nih.gov/pubmed/15750215/

(23) https://www.ncbi.nlm.nih.gov/pubmed/23565496/

(24) https://www.ncbi.nlm.nih.gov/pubmed/22201977/

(25) https://www.ncbi.nlm.nih.gov/pubmed/17049785?dopt=Abstract

(26) https://www.ncbi.nlm.nih.gov/pubmed/17430239/

(27) https://www.ncbi.nlm.nih.gov/pubmed/16340083/

(28) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743662/

(29) https://www.ncbi.nlm.nih.gov/pubmed/18549783

(30) https://www.ncbi.nlm.nih.gov/pubmed/15750215

(31) http://www.karger.com/Article/Abstract/106378

(32) http://link.springer.com/article/10.1007%2Fs40263-013-0076-8

(33) http://jamanetwork.com/journals/jamaneurology/fullarticle/1107947

(34) https://www.ncbi.nlm.nih.gov/pubmed/25008180/

(35) https://www.ncbi.nlm.nih.gov/pubmed/16266773

(36) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260944/

(37) https://www.ncbi.nlm.nih.gov/pubmed/21883804

(38) https://www.ncbi.nlm.nih.gov/pubmed/22710630?dopt=Abstract

(39) https://www.ncbi.nlm.nih.gov/pubmed/21911655?dopt=Abstract

(40) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743662/

(41) https://www.ncbi.nlm.nih.gov/pubmed/219116/

(42) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443484/

(43) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804944/

(44) http://www.ncbi.nlm.nih.gov/pubmed/17942819/

(45) https://www.ncbi.nlm.nih.gov/pubmed/23507773

(46) https://www.ncbi.nlm.nih.gov/pubmed/20719831/

(47) http://www.psyneuen-journal.com/article/S0306-4530(04)00052-6/abstract

(48) https://www.ncbi.nlm.nih.gov/pubmed/15288712

(49) https://www.ncbi.nlm.nih.gov/pubmed/15288712?dopt=Abstract

(50) https://www.ncbi.nlm.nih.gov/pubmed/19091002?dopt=Abstract

(51) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391678/

(52) http://www.news-medical.net/news/2007/10/18/31385.aspx

(53) https://www.ncbi.nlm.nih.gov/pubmed/15288712

(54) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828994/

(55) https://www.ncbi.nlm.nih.gov/pubmed/23107220

(56) https://www.ncbi.nlm.nih.gov/pubmed/25249577

(57) http://www.nature.com/ejhg/journal/v24/n12/full/ejhg2016109a.html

(58) https://www.ncbi.nlm.nih.gov/pubmed/18948358

(59) http://diabetes.diabetesjournals.org/content/63/12/4083.long

(60) https://clinicaltrials.gov/ct2/show/NCT02064166

(61) https://clinicaltrials.gov/ct2/show/NCT02432716

(62) https://www.ncbi.nlm.nih.gov/pubmed/26040423

(63) http://www.ncbi.nlm.nih.gov/pubmed/25374101

(64) https://www.ncbi.nlm.nih.gov/pubmed/18948358

(65) http://www.ncbi.nlm.nih.gov/pubmed/25374101

(66) http://press.endocrine.org/doi/pdf/10.1210/jc.2007-2606

(67) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743662/

(68) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743662/

(69) https://www.ncbi.nlm.nih.gov/pubmed/23719722?dopt=Abstract

(70) https://www.ncbi.nlm.nih.gov/pubmed/15288712?dopt=Abstract

(71) https://www.ncbi.nlm.nih.gov/pubmed/19091002?dopt=Abstract

(72) https://www.ncbi.nlm.nih.gov/pubmed/26777890

(73) https://www.ncbi.nlm.nih.gov/pubmed/15288712

(74) https://www.ncbi.nlm.nih.gov/pubmed/11992114

(75) https://www.ncbi.nlm.nih.gov/pubmed/26855666

(76) https://www.ncbi.nlm.nih.gov/pubmed/12951650

(77) https://www.ncbi.nlm.nih.gov/pubmed/15288712

(78) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804944/

(79) https://www.ncbi.nlm.nih.gov/pubmed/12951650

(80) https://www.ncbi.nlm.nih.gov/pubmed/23107220

(81) https://www.ncbi.nlm.nih.gov/pubmed/24101698

(82) https://www.ncbi.nlm.nih.gov/pubmed/25337926

(83) https://www.ncbi.nlm.nih.gov/pubmed/25374101

(84) https://www.ncbi.nlm.nih.gov/pubmed/20876713

(85) https://www.ncbi.nlm.nih.gov/pubmed/15288712

(86) https://www.ncbi.nlm.nih.gov/pubmed/21911655

Terms and Conditions

Privacy Policy

Affiliate Disclosure

Disclaimer

13 Powerful Ways to Support Your Thyroid & Mental Health

When you know better, you do better.
— Maya Angelou
Picture of the thyroid gland.

Sometimes it may feel as if we have no control over our thoughts and emotions. Our minds can take on a life of their own, with no rhyme or reason as to why we're suddenly sad and anxious.

But there are always underlying causes of these mood swings, and with a better understanding of them, you can learn to manage and overcome them. 

Like I have, you can connect the dots, determine your underlying triggers, learn to control them and even completely eliminate them over time. 

So today I want to talk about thyroid dysfunction. It was one of the underlying issues of my chronic mental illness. 

Your thyroid is a small butterfly-shaped gland located in your neck below your Adam’s apple.

It’s one of your most important glands, producing hormones – thyroxine (T4) and triiodothyronine (T3) – which impact the health and functioning of your entire body.

In fact, normal metabolism and energy levels depend on these hormones. 

Your thyroid also plays a key role in the optimal health and functioning of your brain. It can impact your cognition, concentration, mood, memory and emotions. 

So when your thyroid hormones are out of balance, you can be too, and brain and mental problems can arise.

Your thyroid can either be overactive and produce too much thyroid hormone (hyperthyroidism), or underactive and produce too little thyroid hormone (hypothyroidism).

Hypothyroidism (low thyroid) is much more common, and since I personally struggled with symptoms of hypothyroidism, this post will mostly focus on that.

Picture of thyroid gland.

Hypothyroidism can also be caused by an autoimmune conditions called Hashimoto’s thyroiditis in which the body’s immune system attacks the thyroid tissue.

According to Dr. Datis Kharrazian, author of Why Isn’t My Brain Working? and Why Do I Still Have Thyroid Symptoms?, 90% of people with hypothyroidism have Hashimoto’s. 

Here are some of the common brain and mental health symptoms of low thyroid that I experienced:

  • Chronic fatigue

  • Brain fog

  • Low mood

  • Forgetfulness

  • Weakness

  • Sluggishness

Sounds just like depression, doesn’t it?

 

You Don't Have Mental Illness, You Have Thyroid Problems

Many studies show that people with cognitive, emotional and behavioural disturbances have lower levels of thyroid hormone than the general population, and their psychiatric symptoms improve when they take thyroid hormone.

The following symptoms and disorders have been linked to thyroid problems (69-86): 

  • Depression

  • Anxiety

  • Bipolar disorder, mania and mood swings

  • Irritability and rage

  • Insomnia

  • Paranoid schizophrenia and psychosis

  • Dementia and confusion

  • Social anxiety disorder

  • Generalized anxiety disorder

  • Borderline personality disorder

  • Obsessive-compulsive disorder (OCD)

  • Attention-deficit hyperactivity disorder (ADHD)

In fact, many people struggling with these conditions see better improvements when they are treated with thyroid hormone than when they are treated with psychiatric medication (and experience fewer side effects). 

Psychiatric patients with subclinical hypothyroidism - especially those with incomplete responses to psychotropic therapy - should usually be treated with thyroid hormone. In some patients with no clear evidence of a biochemical or clinical thyroid disorder, mood symptoms nevertheless respond to thyroid hormone.
— Thomas D. Geracioti Jr, MD

A number of different medical practitioners and researchers have written books about how thyroid problems can negatively affect brain and contribute to mental illness:

  • “Brain cells have more thyroid hormone receptors than any other tissue, which means that a proper uptake of thyroid hormone is essential for the brain cells to work properly.” – Dr. Barry Durrant-Peatfield, MD, Author of Your Thyroid and How to Keep It Healthy

  • “How much of what we call “mental illness” is actually thyroid-driven? In my experience, a vast majority.” – Dr. Kelly Brogan, MD, Author of A Mind of Your Own: The Truth About Depression and How Women Can Heal Their Bodies to Reclaim Their Lives

  • "T3 [thyroid hormone] is actually a bonafide neurotransmitter. If you don’t have enough T3, or if its action is blocked, an entire cascade of neurotransmitter abnormalities may ensue, which can lead to mood and energy changes, including depression and anxiety.”– Dr. Christiane Northrup, MD, Author of Women's Bodies, Women's Wisdom: Creating Physical and Emotional Health and Healing

  • “Scientists now consider thyroid hormone one of the major players in brain chemistry disorders. And as with any brain chemical disorder, until treated correctly, thyroid hormone imbalance has serious effects on the patient’s emotions and behavior.” – Dr. Ridha Arem, MD, Author of The Thyroid Solution: A Mind Body Program for Beating Depression and Regaining Your Emotional and Physical Health

  • “There’s a very tight correlation between hypothyroidism and depression. Unfortunately, patients are misdiagnosed with depression when really they have low thyroid. There are well designed clinical trials to show you that your active thyroid hormone is essential to a happy mood. Correcting and nourishing the thyroid gland is absolutely imperative in order to improve mood.” – Suzy Cohen, Author of Thyroid Healthy: Lose Weight, Look Beautiful and Live the Life You Imagine

  • “People with mental health issues have greater rates of thyroid antibodies and Hashimoto's. I've had so many clients who were misdiagnosed. They were on heavy-duty psychotropic medications. They were hospitalized. But it was their thyroid disorder that was causing their issues.” – Dr. Izabella Wentz, PharmD, Author of Hashimoto's Thyroiditis: Lifestyle Interventions for Finding and Treating the Root Cause

So if you struggle with brain or mental illness, you likely do not need a prescription for antidepressants, antipsychotics and anti-anxiety medication. What you really need is to support your thyroid. Treating the underlying thyroid problem is critical to alleviating the associated psychiatric symptoms.

Luckily, there are easy, natural ways for you to do just that.

Below are 13 main strategies I’ve used to balance my thyroid hormones and improve thyroid function. 

Before implementing all of them, I highly recommend getting a full thyroid panel so that you know your starting point.

Click here to subscribe

1. Cut Out Gluten

Certain foods can disrupt proper thyroid function and you should avoid them to optimize brain and mental health. 

Gluten-containing grains (barley, wheat, rye, spelt) are the worst offenders.  

Picture of bread and bagels, which are full of gluten and worsen thyroid function.

The problem with gluten is that it can increase intestinal permeability (leaky gut syndrome). When this happens, small particles of food can leak into your bloodstream. Your immune system sees these food particles as foreign entities and attacks them, increasing inflammation throughout your body. 

On top of this, the molecular structure of gliadin (the protein found in gluten) resembles that of the thyroid gland. So when gliadin enters your bloodstream, your immune system not only attacks the gliadin, but also your thyroid tissue because of its close resemblance. And this can cause many brain and mental health problems (11-13). 

Research shows that people with celiac disease and gluten intolerance are more likely to have thyroid diseases and mental illnesses, and vice versa (1-10). 

Many people that have hypothyroidism really have gluten sensitivity. Over time, they actually have significant brain degeneration. When people degenerate their brain, one of the first things they get is depression.
— Dr. Datis Kharrazian

Thyroid function, and therefore brain and mental health, will often improve after the elimination of gluten-containing grains. 

 

2. Eat Enough Calories and Carbohydrates

Making sure you eat enough calories and carbohydrates on a daily basis is critical for optimal thyroid and brain function.  

A landmark paper, known as the Vermont Study, found that thyroid hormone drops when you don’t eat enough calories and carbohydrates (14). 

Person holding potatoes in their hands.

Several other studies also show that ketogenic low-carb diets can suppress thyroid function and reduce thyroid hormone. This is because carbohydrates play a key role on the production of thyroid hormone (15-18). 

In previous posts, I have mentioned that fasting and ketogenic dieting can have beneficial effects on your brain. This is still true. However, it's important to note fasting and low-carb diets should be followed intermittently and not consistently over long stretches of time, mainly because of their detrimental effects on the thyroid. I prefer to take exogenous ketones instead. They immediately increase my mental clarity without having to restrict carbohydrates. 

My Free Grocery Shopping Guide for Optimal Brain Health contains plenty of healthy, nutrient-dense sources of carbohydrate, including:

  • Yams

  • Squash

  • Potatoes

  • Carrots

  • Other root vegetables

  • Berries

  • Apples

  • Bananas

  • Raw honey

 

3. Avoid Vegetable Oils

You should also significantly limit all refined vegetable oils, including soybean, corn, safflower, sunflower, and canola. 

These oils are predominantly made up of omega-6 polyunsaturated fatty acids (PUFAs), which are highly unstable and oxidize very easily within your body. 

Unfortunately, like gluten, rancid PUFAs are everywhere and hard to avoid. Most commercially-prepared processed foods include them. 

And your thyroid is particularly vulnerable to their effects.

Dr. Raymond Peat, PhD, says that the sudden increase of fragile and rancid polyunsaturated oils into our food supply after World War II has caused many changes in human health, particularly thyroid function and hormones: 

Their [polyunsaturated oils] best understood effect is their interference with the function of the thyroid gland. Unsaturated oils block thyroid hormone secretion, its movement in the circulatory system, and the response of tissues to the hormone. By 1950, then, it was established that unsaturated fats suppress the metabolic rate, apparently creating hypothyroidism. The more unsaturated the oils are, the more specifically they suppress tissue response to thyroid hormone, and transport of the hormone on the thyroid transport protein. And in 1980, experimenters demonstrated that young rats fed milk containing soy oil incorporated the oil directly into their brain cells, and had structurally abnormal brain cells as a result.
Click here to subscribe

4. Eat coconut oil

I’ve discussed the brain and mental health benefits of coconut oil before here

It can help reduce brain fog and enhance your cognitive performance. And it may be accomplishing this by supporting your thyroid. 

According to Dr. Raymond Peat, coconut oil is very beneficial to the brain and thyroid:

Coconut oil has a general pro-thyroid action by diluting and displacing anti-thyroid unsaturated oils. And brain tissue is very rich in complex forms of fats. An experiment in which pregnant mice were given diets containing either coconut oil or unsaturated oil showed that brain development was superior in the young mice whose mothers ate coconut oil. Because coconut oil supports thyroid function, and thyroid governs brain development, including myelination, the result might simply reflect the difference between normal and hypothyroid individuals.

And you don’t need to stick with coconut oil. Coconut milk, water and meat are other ways to get the benefits of coconut. 

 

5. Try Low-level Laser Therapy (LLLT)

Low-level laser therapy (LLLT) is probably the best cutting-edge way to support your thyroid. I wrote about it previously here.  

Using it on my thyroid has made a remarkable difference in my energy levels and mental clarity. And this is likely because of an increase in my thyroid hormones. 

Multiple studies show that LLLT can improve the production of thyroid hormones and improve thyroid function in patients with chronic autoimmune thyroid disease. Study participants were able to reduce the dosage of their thyroid medication (36, 37).  

A study from Brazil showed that LLLT not only reduced the need for thyroid medication in all patients, but 9 months later after the study concluded, it also showed that 47% of patients no longer required any thyroid medication at all.  Participants with Hashimoto’s thyroiditis also saw a reduction in their anti-thyroid antibodies by more than 39% (40). 

A Russian study also demonstrated a 97% success rate when treating women with subclinical hypothyroidism. Researchers concluded LLLT should be the “method of choice in the treatment of [subclinical hypothyroidism], especially in the elderly” (40). 

Animal research has found similar results in rats and rabbits (38, 39). 

I shine the Optimal 1000 Brain Photobiomodulation Therapy Light (Combo Red/NIR) device on my thyroid. It includes both red and infrared light. I’m convinced most people would benefit from it.

When I’m travelling, I take this smaller and more convenient device with me.

Infrared saunas are another excellent way to expose yourself to infrared light and support thyroid function. Check out my post about the benefits here

 

6. Get Enough Vitamin A and D

Fat soluble vitamins A and D are also critical for optimal thyroid and brain function.

Illustration of the sun with “Vitamin D” in the middle.

Vitamin D is necessary to help transport thyroid hormone into your cells and deficiency is quite common in people with thyroid problems. Vitamin D deficiency is also associated with thyroid disease and supplementation has been shown to benefit the thyroid. (22-24). 

I previously discussed the brain health benefits of vitamin D here.

You should test and monitor your Vitamin D levels regularly.

Vitamin A helps your body produce thyroid hormone and protects the thyroid gland from oxidative stress (which is higher in people with thyroid issues). Research also shows that vitamin A can reduce your risk of hypothyroidism (19-21). 

However, I personally don’t recommend you supplement with vitamin A. It’s better to get it from food. Pastured eggs, grass-fed liver and butter (or ghee if you can't tolerate butter) are ideal sources. 

Cod liver oil is another great option as it contains both vitamin A, vitamin D and omega-3 fatty acids all together. I take it every so often.

 

7. Get Enough Minerals

Your thyroid gland needs specific trace minerals to do its job properly. 

I take and recommend a multi-mineral supplement so that you have all the minerals you need to support brain and thyroid health. It includes a small amount of iodine, selenium, magnesium and zinc.

Iodine is the most important, as it’s one of the building blocks used by your thyroid to create hormones. 

However, I don’t recommend supplementing with large doses of iodine separately. Many functional medicine practitioners that I’ve learned from over the years have told me that high iodine intake through supplements can often do more harm than good. Too much supplemental iodine has been shown to cause further thyroid problems (66-68). 

Brazil nuts contain selenium, which can support your thyroid.

So I think the small amount in a multi-mineral is enough.

And getting some more iodine from whole foods, including seafood and sea vegetables, can also benefit you since they contain other nutrients that can support your thyroid.  

Selenium is another indispensable mineral for your thyroid and brain health.

It helps regulate and recycle your iodine stores, and selenium-based proteins help regulate thyroid hormone synthesis and metabolism.

Without it, you’ll likely experience low-thyroid symptoms.

Brazil nuts are the richest dietary source of selenium. 

Low levels of zinc can also lead to depleted thyroid hormones, and vice versa (34). This is just another reason to supplement with zinc.

As I’ve discussed before, a zinc deficiency can also contribute to stress and anxiety.

And although it isn't mentioned very often, magnesium is also critical for optimal thyroid function. The thyroid gland can't function properly without it (89).

I previously discussed how it can help a lot of people with depression and anxiety here

Click here to subscribe

8. Reduce Stress and Cortisol

High levels of physical and mental stress can be detrimental to your thyroid function. 

Your adrenal glands –  two walnut-shaped glands that sit atop the kidneys – secrete your stress stress hormones, such as cortisol, epinephrine and norepinephrine. 

Research shows that cortisol inhibits thyroid hormones from getting into your cells, and weakened adrenal glands can lead to hypothyroid symptoms over time (35).

That’s why it’s critical that you manage stress.

I highly recommend you try to do something every day to manage it. 

The most effective way to significantly and permanently reduce your stress and anxiety is neurofeedback. It’s advanced, guided meditation and I previously wrote about my experience with it here

Person meditating outside.

If you can’t access neurofeedback, taking up a daily meditation practice is an excellent idea. 

I’m a big fan of the Muse headband . It can guide your meditation. Similar to neurofeedback, it gives you real-time feedback while you meditate. I wrote an entire review about it here, and you can get it through the Muse website

I also find massage, acupuncture, heart-rate variability (HRV) training and an acupressure mat very helpful as well.

Lying on the acupressure mat while using my EmWave2 for just 10 minutes relaxes my entire body and mind. I do this at night before bed. 

Supplements that can help with stress include zinc, ashwagandha and phosphatidylserine, which have been shown to lower cortisol levels (87, 88). 

This anti-anxiety supplement also includes a number of natural compounds that have helped me manage my stress over the years.

Lastly, you should get enough sleep and don’t exercise too much. The stress caused by excessive exercise can wear you’re your body and contribute to thyroid problems. So make sure you get plenty of rest and recover between workout sessions.

 

9. Take Thyroid-Supporting Herbs

A number of different herbs can assist your thyroid gland. 

Ashwagandha is one of my favourites. Not only can it reduce stress and anxiety, but a number of studies show that it can boost thyroid hormones (25-29).

Bacopa is another adaptogen that has been shown to increase thyroid (T4) hormone levels by 42% (30). 

Forskolin stimulates the release of thyroid hormones (31). 

And one study found that ginseng increases and normalizes thyroid hormone levels (32). 

And last but not least, researchers say that rhodiola can “improve the quality of life of patients with short-term hypothyroidism” (33). 

Rhodiola also has a number of brain and mental health benefits. I explored them previously here

I’ve experimented with all of these herbs and they have improved my brain and mental health.

But it’s good to know they have some beneficial effects on my thyroid as well.

 

10. Eat “Head to Tail”

Whole plant foods tend to be much healthier when they’re left whole, as they tend to have various nutrients that work together synergistically. 

The same can be said about animal food. 

Muscle meats contain so much tryptophan and cysteine that a pure meat diet can suppress the thyroid. In poor countries, people have generally eaten all parts of the animal, rather than just the muscles – bones, cartilage, skin, organs, and other odd bits. About half of the protein in an animal is collagen, and collagen is deficient in tryptophan and cysteine. This means that, in the whole animal, the amino acid balance is similar to the adult’s requirements.
— Dr. Raymond Peat

In other words, muscle meat (chicken breasts, lean beef) shouldn’t be your only source of animal protein. Our ancestors didn’t eat this way, so neither should we.  

Your body and thyroid prefer and expect to receive a balance of amino acids from different parts of whole animals.

That’s why I recommend “head-to-tail eating” – consuming a wide variety of proteins from the entire animal. 

Along with muscle meat, you should regularly cook and eat organ meats such as liver and bone broth.

Jars of bone broth.

Bone broth contains collagen, gelatin and amino acids such as glycine and proline that help the body better metabolize muscle meat.

Organ meats such as liver have an abundance of beneficial nutrients that aren’t found in muscle meat alone. For example, it’s much higher in vitamin A, which is important for optimal thyroid health (19, 20). 

I previously discussed the benefits of liver in more depth here.

I personally don’t like the taste of liver and bone broth can be inconvenient to make all the time, so I often supplement with grass-fed beef liver capsules and drink high-quality pre-made bone broth.

I also take a Multi-Glandular For Men, which contains a number of different organ tissues. There is also one for women. 

But if you’re actually interested in learning about how to cook and incorporate more whole animal proteins into your diet, I recommend checking out the book Odd Bits: How to Cook the Rest of the Animal by Jennifer McLagan.

 

11. Limit Halogens

Your thyroid doesn’t know the difference between iodine, and other halogens such as bromine, fluorine, chlorine, and perchlorate, which are often found in tap water. 

So your thyroid soaks them up and uses them like iodine.

By occupying iodine receptors, they worsen iodine deficiency, inhibit the production of your thyroid hormones and contribute to thyroid dysfunction.

Studies show that chlorine interferes with proper conversion of thyroid hormone (50, 58-61). 

That’s why I recommend filtering your drinking and shower water. Brita filters aren't enough because they don’t remove fluoride. I use this water filter to make sure I’m drinking the purest water available. It filters everything out of the water. I also use this filter to remove chlorine from my shower water. 

The research shows that bromide in particular can cause a lot of problems. Bromide is found in pesticides, prescription medication, plastic products and personal care products. PBDE (bromide) fire retardants have been added to mattresses, carpeting, electronics, furniture and car interiors since the 1970s. 

Even small amounts of bromide can be problematic, depleting iodine and weakening the thyroid gland. Bromide levels are 50 times higher in thyroid cancer than normal thyroid tissue, and elevated levels of bromide have been linked to mental illness, including depression and schizophrenia (50-57). 

 

12. Avoid Environmental and Dietary Mycotoxins

Mycotoxins – toxic metabolites produced by mold – can also disrupt normal thyroid function.

Mycotoxins are released into the air in water-damaged buildings, and you may not realize it’s affecting your brain and thyroid health until you develop certain symptoms. And even then, people frequently won’t make the connection between the mold and their health. 

That’s what happened to me, and my hormonal health went downhill, along with my brain and mental health. Luckily I’ve recovered since then

Mycotoxins are known hormone disruptors that cause inflammation, and a couple of studies mention that there is an increased frequency of “thyroid, immune dysfunction and autoimmune conditions” in people exposed to water-damaged building (41, 42). 

Very moldy home and man trying to clean it.

And one study shows that mold exposure is correlated with hypothyroidism and Hashimoto’s thyroiditis (43). 

Kurt and Lee Ann Billings wrote the book Mold: The War Within after extensive personal bouts with toxic mold exposure. They write extensively about their experience and recovery and describe ongoing problems with thyroid dysfunction. 

After I moved out of the moldy home, I became extremely sensitive to any environmental mold and mycotoxins. 

I now use an air filter in my apartment. It removes any mold spores and smoke that may be in the air.

Low amounts of mycotoxins are often found in some seemingly healthy foods, such as tea, nuts, grains, coffee and chocolate. I recommend finding the freshest, highest-quality, organic versions of these foods.

Lastly, if exposed to mold or their toxins, you should supplement with activated charcoal or bentonite clay.

Activated charcoal and bentonite clay are potent natural treatments that can trap toxins and chemicals, allowing them to be flushed out of your body.

 

13. Avoid and Remove Other Environmental Toxins

Mold and other halogens aren’t the only endocrine disruptors in your environment that can affect your thyroid metabolism and function.

In the book Thyroid Mind Power, Dr. Karilee Shames reports that “the last 40 years have witnessed a massive increase in the amount of hormone-disrupting synthetic chemicals, finding their way into our air, food and water. The most sensitive and highly susceptible of human tissues turned out to be the thyroid gland.”

Here are some common ones:

Water bottle. The plastic in water bottles can disrupt the thyroid.
  • Bisphenol A – found in plastic bottles and containers. I recommend you only eat and drink out of glass, ceramic and stainless steel. Avoid storing any of your food in plastic too. BPA-free plastic isn’t much better for you and can still disrupt hormonal health.

  • Perfluorooctanoic acid (PFOA) – found in common household products including non-stick cookware and waterproof fabrics. Researchers have found that people with higher levels of PFOA (perfluorooctanoic acid) have a higher incidence of thyroid disease (44, 45).

  • Other pesticides and chemical additives – You should avoid processed food and eat organic as often as possible, wash all produce thoroughly to minimize your pesticide exposure, and find personal care products that don’t include toxic chemicals.

I also recommend increasing your levels of glutathione – your body’s main antioxidant and master detoxifier – to help your body combat the above substances from your body. I do this by supplementing with glutathione on regular basis. 

Or you could take NAC and Vitamin C to help your body produce more of its own glutathione. 

Researchers have found that a decrease in thyroid function could be reversed by NAC supplementation, which increased glutathione. This is because glutathione plays a key role in the production and conversion of your thyroid hormones (46-49). 

Epsom salt baths, infrared saunas, and turmeric can also help your body release and remove environmental toxins. 

 

Summary and Conclusion

With the right information, you can make simple choices to improve thyroid health.

Here's a summary of everything we've gone over:

Doctor holding a woman’s neck to monitor her thyroid.
  • Cut out gluten-containing grains (barley, wheat, rye, spelt)

  • Don't follow a long-term ketogenic low-carb diet and eat enough calories and healthy sources of carbohydrates. See my free food guide for plenty of options. And consider taking exogenous ketones to get the cognitive benefits of a ketogenic diet without actually having to follow the diet.

  • Avoid refined vegetable oils, including soybean, corn, safflower, sunflower, and canola

  • Eat coconut oil

  • Try low-level laser therapy (LLLT)

  • Supplement with Vitamin D, and make sure you get enough Vitamin A from egg yolks, grass-fed liver and ghee

  • Take a multimineral with iodine, selenium and zinc

  • Reduce stress with deep sleep, massage, acupuncture, meditation, neurofeedback, the Muse headband, an acupressure mat, the EmWave2, ashwagandha and phosphatidylserine

  • Take herbs such as bacopa, ginseng, forskolin and rhodiola

  • Eat beef liver and bone broth

  • Filter your drinking water with a filtration system to avoid fluoride, chlorine and other halogens

  • Avoid mold, mycotoxins and other environmental toxins, and protect yourself from them with an air filter, activated charcoal and glutathione

So with that, I want to leave you with a quote from a book I read recently by Sam Harris, called Free Will.

I think this quote is appropriate considering the wide variety of factors that underlie brain and mental health problems:

Becoming sensitive to the background causes of one’s thoughts and feelings can - paradoxically - allow for greater creative control over one’s life. It is one thing to bicker with your wife because you are in a bad mood; it is another to realize that your mood and behaviour have been caused by low blood sugar. This understanding reveals you to be a biochemical puppet, of course, but it also allows you to grab hold of one of your strings: A bite of food may be all your personality requires. Getting behind our conscious thoughts and feelings can allow us to steer a more intelligent course through our lives (while knowing, of course, that we are ultimately being steered).

So even though it seems like there are an overwhelming amount of “strings” to pull, realize that you don’t have to pull them all at once.

You just have to start with one, and go from there.

And then over time, you'll start to get a handle on all of them, and you'll heal.

 
Click here to subscribe

Live Optimally,

Jordan Fallis

Connect with me

References:

(1) http://www.ncbi.nlm.nih.gov/pubmed/11280546

(2) http://www.ncbi.nlm.nih.gov/pubmed/12217453

(3) http://www.ncbi.nlm.nih.gov/pubmed/11123714

(4) http://www.ncbi.nlm.nih.gov/pubmed/10529537

(5) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111403/

(6) http://www.eje-online.org/content/130/2/137.abstract

(7) http://www.ncbi.nlm.nih.gov/pubmed/15244201

(8) http://www.ncbi.nlm.nih.gov/pubmed/9872614

(9) http://www.ncbi.http://www.ncbi.nlm.nih.gov/pubmed/12919165lm.nih.gov/pubmed/12919165

(10) http://www.ncbi.nlm.nih.gov/pubmed/11768252

(11) http://www.ncbi.nlm.nih.gov/pubmed/12366374

(12) http://www.ncbi.nlm.nih.gov/pubmed/19014325

(13) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1808742/

(14) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC371281/

(15) http://www.ncbi.nlm.nih.gov/pubmed/6761185

(16) http://www.ncbi.nlm.nih.gov/pubmed/3740086

(17) http://ajcn.nutrition.org/content/35/1/24.full.pdf

(18) http://www.ncbi.nlm.nih.gov/pubmed/1249190

(19) http://www.ncbi.nlm.nih.gov/pubmed/6470830

(20) http://www.ncbi.nlm.nih.gov/pubmed/23378454

(21) http://ajcn.nutrition.org/content/34/8/1489.abstract

(22) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921055/

(23) http://www.ncbi.nlm.nih.gov/pubmed/12919165

(24) http://www.ncbi.nlm.nih.gov/pubmed/10750047

(25) http://www.ncbi.nlm.nih.gov/pubmed/19789214

(26) http://www.ncbi.nlm.nih

(27) http://onlinelibrary.wiley.com/doi/10.1211/146080800128735782/abstract

(28) http://www.ncbi.nlm.nih.gov/pubmed/9811169

(29) http://www.ncbi.nlm.nih.gov/pubmed/10619390

(30) http://www.sciencedirect.com/science/article/pii/S037887410200048X

(31) http://www.ncbi.nlm.nih.gov/pubmed/6327383

(32) http://www.ncbi.nlm.nih.gov/pubmed/6327383

(33) http://www.ncbi.nlm.nih.gov/pubmed/20946017

(34) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746228/

(35) http://www.ncbi.nlm.nih.gov/pubmed/17002934

(36) http://www.ncbi.nlm.nih.gov/pubmed/20662037

(37) http://www.ncbi.nlm.nih.gov/pubmed/22718472

(38) http://www.ncbi.nlm.nih.gov/pubmed/25265487

(39) http://www.ncbi.nlm.nih.gov/pubmed/25975382

(40) http://valtsus.blogspohttp://va

(41) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654247/

(42) http://www.ncbi.nlm.nih.gov/pubmed/15143854

(43) http://www.ncbi.nlm.nih.gov/pubmed/430949

(44) http://www.ncbi.nlm.nih.gov/pubmed/24407430

(45) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866686/

(46) http://www.ncbi.nlm.nih.gov/pubmed/21540553?dopt=Abstract

(47)https://www.researchgate.net/publication/12044880_Effect_of_Glutathione_GSH_Depletion_on_the_Serum_Levels_of_Triiodothyronine_T_3_Thyroxine_T_4_and_T_3_T_4_Ratio_in_Allyl_AlcoholTreated_Male_Rats_and_Possible_Protection_With_Zinc

(48) http://www.ncbi.nlm.nih.gov/pubmed/7408784

(49) http://www.ncbi.nlm.nih.gov/pubmed/7052928

(50) http://www.ncbi.nlm.nih.gov/pubmed/8909694

(51) http://www.ncbi.nlm.nih.gov/pubmed/15255296

(52) http://www.ncbi.nlm.nih.gov/pubmed/10999431

(53) http://www.ncbi.nlm.nih.gov/pubmed/9542578

(54) http://www.ncbi.nlm.nih.gov/pubmed/9341949

(55) http://www.ncbi.nlm.nih.gov/pubmed/8909694

(56) http://www.ncbi.nlm.nih.gov/pubmed/6548284

(57) http://www.ncbi.nlm.nih.gov/pubmed/8909694

(58) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890436/

(59) http://www .ncbi.nlm.nih.gov/pubmed/1087230

(60) http://www.ncbi.nlm.nih.gov/pubmed/19318504

(61) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956646/

(62) http://www.ncbi.nlm.nih.gov/pubmed/9140329

(63) http://www.ncbi.nlm.nih.gov/pubmed/21001996

(64) www.gulflink.osd.mil/library/randrep/pb_paper/mr1018.2chap10.html

(65) http://www.optimox.com/iodine-study-18

(66) http://www.ncbi.nlm.nih.gov/pubmed/7477223

(67) http://www.ncbi.nlm.nih.gov/pubmed/20517655?dopt=AbstractPlus

(68) http://www.eymj.org/Synapse/Data/PDFData/0069YMJ/ymj-44-227.pdf

(69) https://www.ncbi.nlm.nih.gov/pubmed/15213796

(70) http://www.drrichardhall.com/Articles/hashimoto.pdf

(71) http://www.ncbi.nlm.nih.gov/pubmed/11958781

(72) http://www.ncbi.nlm.nih.gov/pubmed/17141745

(73) http://bmcpsychiatry.biomedcentral.com/articles/10.1186/1471-244X-4-25

(74) http://cpementalhealth.biomedcentral.com/articles/10.1186/1745-0179-1-23

(75) http://www.ncbi.nlm.nih.gov/pubmed/19215985

(76) http://www.ccjm.org/indhttp://www.ccjm.org/index.php?id=107937&tx_ttnews[

(77) http://www.health.harvard.edu/diseases-and-conditions/thyroid-deficiency-and-mental-health

(78) http://www.ncbi.nlm.nih.gov/pubmed/20404728

(79) http://www.ncbi.nlm.nih.gov/pubmed/27268005

(80) http://www.ncbi.nlm.nih.gov/pubmed/24480318

(81) http://www.ncbi.nlm.nih.gov/pubmed/24480318

(82) http://www.eje-online.org/content/138/1/1.full.pdf

(83) http://www.ncbi.nlm.nih.gov/pubmed/24443228

(84) http://www.ncbi.nlm.nih.gov/pubmed/24345793

(85) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013313/

(86) http://www.ncbi.nlm.nih.gov/pubmed/23380316

(87) http://www.ncbi.nlm.nih.gov/pubmed/23439798

(88) http://www.ncbi.nlm.nih.gov/pubmed/1325348

(89) http://www.ncbi.nlm.nih.gov/pubmed/6747732

Terms and Conditions

Privacy Policy

Affiliate Disclosure

Disclaimer