Category: Pain / Inflammation

Today I wanted to share with you some published research which suggests that a common and readily accessible nutritional compound – 5-HTP may be able to mitigate the severity of Rheumatoid Arthritis (RA) and if it is consumed early on in the development stage of RA that it may in fact prevent the RA from developing.

Note that this study was done using an animal model – mice.

Rheumatoid Arthritis

From the Rheumatoid Arthritis. org website:


Rheumatoid arthritis (RA) is a complex disease that affects each patient differently. People from all ethnic backgrounds are at risk of developing RA. It is the third most common type of arthritis behind osteoarthritis and gout.

RA Facts and Statistics

RA is a chronic disease affecting over 1.3 million Americans and as much as 1% of the worldwide population. The specific cause of RA is not known, and as a result there is no known cure for the disease.

Researchers do know, however, that RA is the result of an autoimmune disorder. It is one of the most common autoimmune disorders – more common than psoriasis, Crohn’s disease, multiple sclerosis, and lupus. RA symptoms are triggered when a person’s antibodies mistakenly attack the normal synovial joint fluid, causing chronic inflammation.

Women are up to three times more likely to develop RA than men. Women are also more likely to develop the disease at a younger age than men. RA generally begins to affect people between the ages of 30 and 60 years old. The average person doesn’t develop symptoms of RA until they reach their 60’s.

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Following is an article from the Life Enhancement website which discusses this published research on 5-HTP for RA

Here is the link to the actual abstract if you want to review it.


In the article, it suggests that 5-HTP can be useful for Asthma, Depression, Obesity, Headaches, Fibromyalgia, Insomnia, and Arthritis.

Regards,

Rob


In addition to its use as an antidepressant …

New research brings additional clarity to the mechanisms of 5-HTP

The amino acid tryptophan is essential for humans, meaning the body cannot synthesize it and must obtain it from the diet. A tryptophan deficiency can lead to serious emotional imbalances as well as diminished neural health.

In part, this is because tryptophan is a precursor to serotonin and melatonin. To synthesize these, tryptophan drives two major metabolic pathways: the serotonin pathwayand kynurenine pathway.

The Pathway to Well-Being and Happiness

In the serotonin pathway, tryptophan is catalyzed into 5-hydroxytryptophan (5-HTP) by tryptophan hydroxylase-1 and then converted into serotonin. Biochemically derived from tryptophan or 5-HTP, serotonin is principally found in the gastrointestinal tract, blood platelets, and the central nervous system of humans and animals. Serotonin is generally thought to be a contributor to feelings of well-being and happiness.

Does Kynurenine Provide a Pathway to Inflammation?

A tryptophan deficiency can lead to 
serious emotional imbalances as well 
as diminished neural health.

In the kynurenine pathway, tryptophan is catalyzed into N-formylkynurenine by indoleamine 2,3 dioxygenase (IDO) and then converts into L-kynurenine. L-kynurenine is a metabolite of the amino acid L-tryptophan used in the production of niacin. However, the Kynurenine pathway is a mixed bag. Rheumatoid arthritis patients have increased kynurenine levels in their blood1,2 and its levels are positively correlated with C- Reactive Protein (CRP), a measure of inflammation.3

Serotonin is generally thought to be a 
contributor to feelings of well-being 
and happiness.

5-HTP Suppresses Inflammatory Responses 

In a new Taiwan study,4 researchers note that 5-HTP suppresses inflammatory responses in mouse models of asthma and sepsis. In prior studies, 5-HTP inhibited the production of pro-inflammatory mediators in different cell lines. These associations stimulated the researchers interest in whether 5-HTP could suppress inflammation and disease activity in collagen-induced arthritis (CIA) in mice. CIA is an animal form of human rheumatoid arthritis (RA).

The Value of Rheumatoid Arthritis’s Therapeutic Window

Evidence is accumulating that a preclinical phase is present before the onset of clinical signs and symptoms of RA. This phase represents an important therapeutic window within which interventions can dramatically modulate outcomes.

RA is a chronic inflammatory disorder that, unlike the wear-and-tear damage of osteoarthritis, typically affects the small joints in the hands and feet. RA also affects the lining of joints, causing a painful swelling that can eventually result in bone erosion and joint deformity. RA can occur at any age, although it usually begins after age 40 and is much more common in women.

Preventative Desired

An agent that could prevent RA in the preclinical phase would be a novel approach. In this study, the Taiwan researchers investigated whether the tryptophan metabolite, 5-HTP, could act as such an agent for the primary prevention of CIA. The CIA mouse model is the most commonly studied autoimmune model of rheumatoid arthritis. It is widely used to address questions of disease pathogenesis and to validate therapeutic targets.

5-HTP suppresses 
inflammatory responses in mouse 
models of asthma and sepsis.

5-HTP Suppressed Cell Proliferation

The Taiwan researchers found that 5-HTP given at 10, 20 and 50 μg/ml suppressed cell proliferation and decreased the production of Interleukin (IL)-22 type cells, which regulate the pathogenesis of autoimmune diseases.

5-HTP also suppressed the expression of IL-17, TNFα, IFNγ and T-bet in activated splenocytes (spleen cells). These findings did not result from cell death, because 5-HTP did not increase cell death at these levels.

It’s a Matter of Timing

In their animal studies, a supplement of 5-HTP from day 20 did not affect the disease course. However, 5-HTP given from day 7 before induction significantly decreased the arthritis scores and joint inflammation. Earlier was better than later.

5-HTP May Prevent RA

According to the Taiwan study, patients with allergy/asthma commonly have associated symptoms of anxiety/depression. These results suggest that 5-HTP supplements can be an approach to prevent arthritis.

5-HTP taken orally suppressed allergic lung inflammation, even though cytokine levels were not decreased on broncho-alveolar lavage (BAL).5 BAL is a medical procedure in which a bronchoscope is passed through the mouth or nose into the lungs and fluid is squirted into a small part of the lung and then collected for examination. It is typically performed to diagnose lung disease. (See “Galantamine Protects Against Lung Injury,” the sidebar in the lead article “Stop Smoking with Galantamine” in this issue.)

5-HTP given from day 7 before 
induction significantly decreased the 
arthritis scores and joint 
inflammation.

Serotonin and Major Depressive Disorders

Decreased levels of serotonin in the central nervous system are associated with major depressive disorders. Treatment with selective serotonin reuptake inhibitors (SSRIs) or supplementation with serotonin precursors (tryptophan and 5-HTP) is an important strategy in depression therapy. SSRIs can block serotonin re-uptake and thus increase serotonin levels in the brain and improve depression. Tryptophan and 5-HTP can make serotonin in the body and also improve depression.

SSRIs and Supplements

Of interest, certain SSRIs can decrease the production of pro-inflammatory cytokines, suppress airway inflammation in asthma patients, and reduce disease activity in RA patients. SSRIs have also been found to decrease the arthritis scores in CIA mice and suppress cytokine production in macrophages and synovial membrane cells. But SSRIs are not without adverse effects.

Patients with allergy/asthma 
commonly have associated symptoms 
of anxiety/depression.

The Taiwan researchers found that the SSRI fluoxetine (aka Prozac) effectively decreased the production of IFNγ and TNFα in activated splenocytes. In the animal study, it was found that 5-HTP given orally increased the serum levels of serotonin, whereas parenteral 5-HTP did not affect the serum levels of serotonin in CIA mice. Thus, regulation of serotonin levels is not likely to be the major mechanism behind the suppression of arthritis by 5-HTP in the CIA mice.

RA patients have increased kynurenine levels in the blood, and the levels are positively correlated with C-reactive protein. In addition, RA patients have increased indoleamine 2,3 dioxygenase (IDO) activity in the synovial fluid.

5-HTP Regulates Immune Responses

The Taiwan study provides both in vitro and in vivo evidence that 5- HTP, a tryptophan metabolite, can regulate immune responses. Taking a 5-HTP supplement before CIA induction can decrease disease activity, suppress joint inflammation and cause minimal side effects in CIA mice. Nevertheless (you’ve undoubtedly heard this before), further studies are required to elucidate whether the common dietary supplement 5-HTP can act as an agent for primary prevention of RA.

5-HTP taken orally 
suppressed allergic lung 
inflammation, even though cytokine 
levels were not decreased on 
broncho-alveolar lavage.

Also in the Taiwan study, it was found that 5-HTP did not affect the cytokine levels in the serum or the percentages of IFNγ+CD4+ T cells in the spleen. However, 5-HTP suppressed the expression of TNFα and IL-6 in the inflamed ankle joints and decreased the percentages of IFNγ+CD4+ T cells in the draining lymph nodes. These results suggest that 5-HTP decreased arthritis activity without affecting systemic immunity.

Serotonin Up; Kynurenine Down

Of great interest, pro-inflammatory cytokines such as TNFα, IL-1 and IFNγ can increase IDO expression and promote serotonin re-uptake, resulting in increased levels of kynurenine and decreased levels of serotonin. Indeed, IDO is the first and rate-limiting enzyme of tryptophan catabolism through the kynurenine pathway, thus causing depletion of tryptophan, which can cause halted growth of microbes as well as T cells.

The study showed that mice with a higher arthritis score were more likely to have high serum levels of kynurenine and low levels of serotonin.

5-HTP for Asthma, Depression, Obesity, Headaches, Fibromyalgia, Insomnia, and Arthritis

As reported by the Taiwan scientists, in mouse models of asthma, the amount of 5-HTP given to the mice was equivalent to consumption of 200 mg per day by a 100 lb person. In their study, the daily consumption of 5-HTP was equivalent to between 384 mg and 1,920 mg per day by a 132 lb person.

5-HTP given orally increased the 
serum levels of serotonin.

5-HTP is indicated for depression, obesity, headaches, fibromyalgia and insomnia. A 5-HTP supplement is well-tolerated and causes minimal side effects. In clinical studies, the doses of 5- HTP in the treatment of depression have been from 20 to 3,250 mg per day.

Treatment with 5- HTP at 600 mg per day was also found to decrease the frequency of migraine and improve insomnia. In a mouse model of asthma, the amount of 5-HTP given to the mice was equivalent to consumption of 200 mg per day by a 100 lb person.

In the Taiwan animal study, 5-HTP given orally did not affect body weight or cause diarrhea. However, the daily consumption of 5-HTP was equivalent to 384 mg and 1,920 mg per day by a 132 lb person. Furthermore, 5-HTP given by i.p. injection at 30, 100 and 300 mg/kg decreased the production of TNFa in a sepsis model.

These results suggest that 5-HTP 
decreased arthritis activity without 
affecting systemic immunity.

The mice receiving the i.p. amounts at 30, 100 and 300 mg/kg (human equivalents of 160 mg, 527 mg, 1,580 for a 132 lb person) had improved arthritis scores and decreased joint inflammation.

Epstein-Barr virus may be the leading cause of multiple sclerosis

Summary:

A new study provides compelling evidence of causality between Epstein-Barr virus and multiple sclerosis. It suggests that most MS cases could be prevented by stopping EBV infection, and that targeting EBV could lead to the discovery of a cure for MS.

Multiple sclerosis (MS), a progressive disease that affects 2.8 million people worldwide and for which there is no definitive cure, is likely caused by infection with the Epstein-Barr virus (EBV), according to a study led by Harvard T.H. Chan School of Public Health researchers.

Their findings will be published online in Science on January 13, 2022.

“The hypothesis that EBV causes MS has been investigated by our group and others for several years, but this is the first study providing compelling evidence of causality,” said Alberto Ascherio, professor of epidemiology and nutrition at Harvard Chan School and senior author of the study. “This is a big step because it suggests that most MS cases could be prevented by stopping EBV infection, and that targeting EBV could lead to the discovery of a cure for MS.”

MS is a chronic inflammatory disease of the central nervous system that attacks the myelin sheaths protecting neurons in the brain and spinal cord. Its cause is not known, yet one of the top suspects is EBV, a herpes virus that can cause infectious mononucleosis and establishes a latent, lifelong infection of the host. Establishing a causal relationship between the virus and the disease has been difficult because EBV infects approximately 95% of adults, MS is a relatively rare disease, and the onset of MS symptoms begins about ten years after EBV infection. To determine the connection between EBV and MS, the researchers conducted a study among more than 10 million young adults on active duty in the U.S. military and identified 955 who were diagnosed with MS during their period of service.

The team analyzed serum samples taken biennially by the military and determined the soldiers’ EBV status at time of first sample and the relationship between EBV infection and MS onset during the period of active duty. In this cohort, the risk of MS increased 32-fold after infection with EBV but was unchanged after infection with other viruses. Serum levels of neurofilament light chain, a biomarker of the nerve degeneration typical in MS, increased only after EBV infection. The findings cannot be explained by any known risk factor for MS and suggest EBV as the leading cause of MS.

Ascherio says that the delay between EBV infection and the onset of MS may be partially due the disease’s symptoms being undetected during the earliest stages and partially due to the evolving relationship between EBV and the host’s immune system, which is repeatedly stimulated whenever latent virus reactivates.

“Currently there is no way to effectively prevent or treat EBV infection, but an EBV vaccine or targeting the virus with EBV-specific antiviral drugs could ultimately prevent or cure MS,” said Ascherio.

Other Harvard Chan School researchers who contributed to this study include Kjetil Bjornevik, Marianna Cortese, Michael Mina, and Kassandra Munger.

Funding for this study came the National Institute of Neurological Disorders and Stroke, National Institutes of Health (NS046635, NS042194, and NS103891), the National Multiple Sclerosis Society (PP-1912-35234), the German Research Foundation (CO 2129/ 1-1), the National Institutes of Health (DP5- OD028145), and the Howard Hughes Medical Institute.


Story Source:

Materials provided by Harvard T.H. Chan School of Public Health. Note: Content may be edited for style and length.


Journal Reference:

  1. Kjetil Bjornevik, Marianna Cortese, Brian C. Healy, Jens Kuhle, Michael J. Mina, Yumei Leng, Stephen J. Elledge, David W. Niebuhr, Ann I. Scher, Kassandra L. Munger, Alberto Ascherio. Longitudinal analysis reveals high prevalence of Epstein-Barr virus associated with multiple sclerosis. Science, 2022 DOI: 10.1126/science.abj8222

  Harvard T.H. Chan School of Public Health. “Epstein-Barr virus may be leading cause of multiple sclerosis.” ScienceDaily. ScienceDaily, 13 January 2022. <www.sciencedaily.com/releases/2022/01/220113151342.htm>.

I was reminded this morning of the significant potential health benefits of earthing/grounding while watching a program on GAIA.

If you are not familiar with GAIA, it is similar to Netflix but with more of an emphasis on topics such as integrative health, spirituality etc.

In fact I enjoy the content available on GAIA that I rarely watch Netflix any more.

Here is a link to the episode that I watched this morning on earthing/grounding which you can watch for free

Here is an example of what the published research has to say about the potential health benefits of earthing/grounding:
Environ Public Health. 2012; 2012: 291541. Published online 2012 Jan 12. doi: 10.1155/2012/291541 PMCID: PMC3265077PMID: 22291721

Earthing: Health Implications of Reconnecting the Human Body to the Earth’s Surface Electrons

Gaétan Chevalier, 1, 2 ,*Stephen T. Sinatra, 3 James L. Oschman, 4 Karol Sokal, 5 and Pawel Sokal 6

Abstract

Environmental medicine generally addresses environmental factors with a negative impact on human health. However, emerging scientific research has revealed a surprisingly positive and overlooked environmental factor on health: direct physical contact with the vast supply of electrons on the surface of the Earth.

Modern lifestyle separates humans from such contact. The research suggests that this disconnect may be a major contributor to physiological dysfunction and unwellness. Reconnection with the Earth’s electrons has been found to promote intriguing physiological changes and subjective reports of well-being. Earthing (or grounding) refers to the discovery of benefits—including better sleep and reduced pain—from walking barefoot outside or sitting, working, or sleeping indoors connected to conductive systems that transfer the Earth’s electrons from the ground into the body. This paper reviews the earthing research and the potential of earthing as a simple and easily accessed global modality of significant clinical importance.

2.1. Sleep and Chronic Pain

2.3. Earthing Reduces Electric Fields Induced on the Body

2.4. Physiological and Electrophysiological Effects

4.4. Heart Rate Variability

4.5. Reduction of Primary Indicators of Osteoporosis, Improvement of Glucose Regulation, and Immune Response

4.6. Altered Blood Electrodynamics

Table 1

Subjective sleep, pain, and well-being feedback.

CategoriesTest subjects*Control subjects**
SameImprovedSameImproved
Time to fall asleep4 = 15%23 = 85%20 = 87%3 = 13%
Quality of sleep2 = 7%25 = 93%20 = 87%3 = 13%
Wake feeling rested0 = 0%27 = 100%20 = 87%3 = 13%
Muscles stiffness and pain5 = 18%22 = 82%23 = 100%0 = 0%
Chronic back and/or joint pain7 = 26%20 = 74%23 = 100%0 = 0%
General well-being6 = 22%21 = 78%20 = 87%3 = 13%

*Reports not received from three participants.

**Reports not received from seven participants.

4. Conclusion

De Flora et al. wrote the following: “Since the late 20th century, chronic degenerative diseases have overcome infectious disease as the major causes of death in the 21st century, so an increase in human longevity will depend on finding an intervention that inhibits the development of these diseases and slows their progress” [33].

Could such an intervention be located right beneath our feet? Earthing research, observations, and related theories raise an intriguing possibility about the Earth’s surface electrons as an untapped health resource—the Earth as a “global treatment table.” Emerging evidence shows that contact with the Earth—whether being outside barefoot or indoors connected to grounded conductive systems—may be a simple, natural, and yet profoundly effective environmental strategy against chronic stress, ANS dysfunction, inflammation, pain, poor sleep, disturbed HRV, hypercoagulable blood, and many common health disorders, including cardiovascular disease. The research done to date supports the concept that grounding or earthing the human body may be an essential element in the health equation along with sunshine, clean air and water, nutritious food, and physical activity.

This simple behavioral change has the potential to initiate powerful improvements in health conditions and is something that may warrant consideration for everyone.

I want to share with you a podcast I recently guested on that really goes into the science of NAD+, ENERGY and the benefits of Pricera – here is the link: https://lnkd.in/g-EK96G

Here is some  information on our NAD+ precursor formulation – Pricera.

NAD+ levels decline precipitously as we age: it is down 50% by the age of 50 and down 90 – 96% by the age of 80
– one of the key functions of NAD+ is to activate the Sirtuin longevity genes which are critical for healthy aging
– when the Sirtuins are not activated, it accelerates vascular aging which will of course impact on the vascular system  but since the vascular system delivers oxygen and nutrients to every cell in the body, the lack of NAD+ will have a consequential negative impact on virtually EVERY cell in the body and virtually all chronic degenerative conditions

Increased Energy Levels

Certainly reported increased energy (due to Pricera’s impact on the mitochondria) has been widely reported however that is just one reported benefit – and the report often comes in from individuals in good to excellent health.

Others key applications include:

  • Neurodegenerative conditions – such as Parkinson’s
  • Inflammation
  • Addictions
  • Chronic Fatigue Syndrome
  • Exercise performance and recovery
  • Immune system activation
  • Low energy/mitochondrial dysfunctions
  • Blood sugar issues
  • Hypertension
  • Elevated cholesterol levels
  • Mood disorders
  • Oxidative stress

Order Pricera now:

http://www.healthspan-formulations.com

Here are a couple of examples of typical testimonials:

Liking Pricera 🙂

Definitely boosting energy and focus.
It’s been ages since I got out in the evening for a bike ride
just because I was so knackered.

This changed within 2 days of starting the Pricera.
Also more mental clarity.

Chris Spooner, ND
Vernon, BC 

For a number of years I have been dealing with low energy and stamina, Chronic Fatigue and hand tremors. 

One of the key areas where Pricera impacts me is my energy levels – in the past, I often could only work for 4-5 hours before I felt exhausted and would have to stop. 

Some days it felt like my energy levels were so depleted that it was a struggle to get out of bed. 

Since starting on the Pricera, I have experienced a tremendous boost to my energy levels and I can now work 8-10 hours at a stretch. 

I have gained more stamina, energy and clarity and I have seen a significant improvement in my exercise capacity. 

For myself, Pricera has been a life saver, and I will not miss a single day taking it! 

Let me know if you would like any additional information or if you have any questions.

http://www.healthspan-formulations.com

Like many of you, I am constantly tinkering and experimenting with different modifiable lifestyle factors to try to optimize my quality of life – I am truly a biohacker.

As you would know, there is a big difference between Chronological Age and Biological Age.  We have all worked with patients and seen individuals who look a lot older – or younger than their Chronological Age.

There are a lot of factors that can influence this difference: we cannot discount genetics however as we all know epigenetic expression can be significantly influenced by lifestyle and environmental factors.

So factors that we typically help our patients with would be included, such as diet, sleep, exercise, mental attitude, exposure to environmental toxins etc. can influence Biological Age.

When I am working with clients, I use a technology device which I have referred to previously – the iHeart technology which functions as a pulse oximeter but as well it measures AoPWV- Aortic Pulse Wave Velocity which is a measurement of aortic flexibility.

This biomarker is increasingly being used by progressive cardiologists and other health care practitioners as an indication of CV health and the potential for future events including sudden death, strokes and heart attacks. 

This is considered a more accurate predictor of these events vs. lipid panels due to the fact that approximately 40% of individuals who have one of these events have normal lipid panels.

But what I really love about the iHeart is that it has an algorithm which compares Chronological Age vs. Biological Age.

I use this technology with all my clients and I find it works well to convey the concept of Healthspan and to optimize compliance.

I use this device regularly on myself and I get good results: I am 66 years old and my Biological Age result is typically around 25 years of age.

I take a lot of supplements and I have been doing some experimentation recently whereby I would check my Biological Age before and after taking my supplements to see if they were having any impact on my Biological Age results.

And sure enough, recent experimentation has shown that prior to taking my supplements my Biological Age reading was around 40 years – and then an hour or two after taking my supplements it was down to around 25 years of age.

And then I wanted to see if I could determine which of my supplements was having the most significant effect.

Sure enough the most significant impact came from just two supplements which would decrease my Biological Age by approximately 15 years and these two supplements turned out to be our two key Integra Nutrition formulations: Pricera, our very popular NAD+ precursor formulation as well as our GenZogenol formulation.

I won’t go into detail on these two formulations in this article: if you want more details on them, have a look at our Integra Nutrition website.

GenZogenol: this formulation includes a key ingredient – Enzogenol which has been shown in a rat study to LENGTHEN telomeres by 40% and in a mouse study to to lengthen healthspan and lifespan by the equivalent of approximately 15 years in humans.

Pricera: is an NAD+ precursor formulation and according to the published literature the best on the market.***

NAD+ levels decrease by 50% by the age of 50 and they are down by 90-96% by the age of 80.

One key factor about NAD+ is it is necessary to activate the Sirtuin longevity genes so if these are not being activated, it accelerates vascular aging which has an impact on virtually every cell in the body.

Optimizing NAD+ levels can have a significant impact on energy levels due to its impact on mitochondrial function: many users feel a surge in energy levels even within 24-72 hours.

These two formulations can have a dramatic positive impact on your personal aging process and healthsplan.

In addition, they can have a significant positive impact on pretty much all chronic, degenerative conditions.

If you would like to get some additional documentation of these two formulations – including some of the published research, reach out to me.

Pricera Testimonials

Liking Pricera 🙂

Definitely boosting energy and focus.
It’s been ages since I got out in the evening for a bike ride just because I was so knackered.

This changed within 2 days of starting the Pricera.
Also more mental clarity.

Chris Spooner, ND
Vernon, BC

For a number of years I have been dealing with low energy and stamina, Chronic Fatigue and hand tremors.

One of the key areas where Pricera impacts me is my energy levels – in the past, I often could only work for 4-5 hours before I felt exhausted and would have to stop.

Some days it felt like my energy levels were so depleted that it was a struggle to get out of bed.

Since starting on the Pricera, I have experienced a tremendous boost to my energy levels and I can now work 8-10 hours at a stretch.

I have gained more stamina, energy and clarity and I have seen a significant improvement in my exercise capacity.

For myself, Pricera has been a life saver, and I will not miss a single day taking it!

MG Vancouver, BC

I wanted to share with you today an article from Quanta magazine which focuses on “Why Sleep Deprivation Kills”.

We all know about the importance of sleep as an integral component of overall health.

We have all experienced the negative effects of a lack of sleep on our health and cognitive function.

Despite decades of research, sleep is still a poorly understood process and why a lack of sleep can cause such significant negative health effects.

Now it appears that part of the answer to this question may have finally been resolved.

As it suggests in the article, many of us would assume that the origin of these types of issues would be focused in the brain however it turns out that this may not in fact be the case, but rather due to the generation of ROS (Reactive Oxygen Species) in the gut.

It is a bit of a long article so here are the abstract as well as study highlights.

If you want to read the whole article you can click on the link above.

Feeling dead tired? Scientists may finally be on the verge of learning why too little sleep is inevitably fatal.
  Article| Volume 181, ISSUE 6, P1307-1328.e15, June 11, 2020

Sleep Loss Can Cause Death through Accumulation of Reactive Oxygen Species
in the Gut

Published:June 04, 2020DOI:
https://doi.org/10.1016/j.cell.2020.04.049

Highlights

  • Sleep deprivation leads to ROS accumulation in the fly and mouse gut
  • Gut-accumulated ROS trigger oxidative stress in this organ
  • Preventing ROS accumulation in the gut allows survival without sleep in flies

Summary

The view that sleep is essential for survival is supported by the ubiquity of this behavior, the apparent existence of sleep-like states in the earliest animals, and the fact that severe sleep loss can be lethal. The cause of this lethality is unknown.

Here we show, using flies and mice, that sleep deprivation leads to accumulation of reactive oxygen species (ROS) and consequent oxidative stress, specifically in the gut. ROS are not just correlates of sleep deprivation but drivers of death: their neutralization prevents oxidative stress and allows flies to have a normal lifespan with little to no sleep.

The rescue can be achieved with oral antioxidant compounds or with gut-targeted transgenic expression of antioxidant enzymes. We conclude that death upon severe sleep restriction can be caused by oxidative stress, that the gut is central in this process, and that survival without sleep is possible when ROS accumulation is prevented.

Pricera is now available!

PRICERA NAD+ Presursor:

KEY APPLICATIONS

  • Parkinson’s and other neurodegenerative conditions
  • Inflammation
  • Addictions
  • Chronic Fatigue Syndrome
  • Exercise performance and recovery
  • Immune system activation
  • Mitochondrial dysfunction
  • Diabesity Spectrum
  • Hypertension
  • Elevated cholesterol levels
  • Depression
  • Oxidative stress