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Dr. James Wilson

Dr. James Wilson

James L. Wilson D.C., N.D., Ph.D. has helped thousands of people with Adrenal Fatigue regain their health and vitality during his 24 years of private practice.

Natural Medicine, August - November 2018

Exploring Adrenal Fatigue

Natural Medicine, May - August 2018

What is Adrenal Fatigue?

Listner, July 11

Listner, July 11

Stressed to Excess

Wellbeing, Feb 2010

WellBeing, Feb 10

Stress Less

Woman's Weekly Feb 2010

Woman's Weekly Feb 10

A modern-day problem

Listener Jan 09

Listener Jan 09

Relax, don’t diet.

Chronic Stress May Cause Lasting Genetic Changes

 

Long-term exposure to the hormone cortisol may leave a lasting mark on the genome and influence how genes that control mood and behavior are expressed, a study led by Johns Hopkins researchers suggests. The finding, published in the September 2010 issue of Endocrinology, could eventually lead to new ways to explain and treat depression, bipolar disorder, and other mental illnesses.

Scientists and physicians have long been interested in the cause of depression, a sometimes debilitating disorder that affects about 16 percent of people at least once over the course of a lifetime. While studies have shown that many other mental illnesses are strongly heritable, studies have shown that the risk of depression is only about 40 percent genetic. Consequently, environmental factors are thought to play a major role in causing this disease.

Unsurprisingly, previous research has shown that stressful life events can increase the risk of depression. But how these life events play into the biology of this disease is unknown.

James Potash, M.D., M.P.H., an associate professor at the Johns Hopkins University School of Medicine, and colleagues suspected that epigenetic factors might be at work in the disease. Epigenetic, or "above the genome," factors are so named because they affect how genes are expressed without changing the genetic sequence. One of the most prevalent epigenetic changes, or "marks," are methyl chemical groups that clip onto DNA, often shutting off the gene that they attach to.

To see if stress might influence epigenetic marks on genes involved in depression, Potash and his Johns Hopkins colleagues, including study co-leader Gary Wand, M.D., a professor in the Division of Endocrinology, assistant professor Kellie Tamashiro, Ph.D., and postdoctoral fellow Richard Lee, Ph.D., gave some mice corticosterone in their drinking water for four weeks. Corticosterone is the mouse version of cortisol, a hormone produced by the human body during stressful situations. Other mice drank plain water without this hormone.

At the end of the four-week period, the mice who received corticosterone displayed anxious characteristics in behavioral tests. Gene expression tests on these animals showed a marked increase in protein produced by a gene called Fkbp5. This gene’s human form has been linked to mood disorders, including depression and bipolar disease.

When the researchers examined the rodents’ DNA for epigenetic marks on Fkbp5, they found substantially fewer methyl groups attached to this gene in mice that received corticosterone compared with those that didn’t. These differences in epigenetic marks persisted for weeks after the mice stopped receiving the hormone, suggesting long-lasting change.

"This gets at the mechanism through which we think epigenetics is important," says Potash, who directs Johns Hopkins’ Mood Disorders Research Programs.He explains that epigenetic marks that are added through life experience may prepare an animal for future events. "If you think of the stress system as preparing you for fight or flight, you might imagine that these epigenetic changes might prepare you to fight harder or flee faster the next time you encounter something stressful."

These behaviors, which were probably advantageous earlier in evolution, aren’t as useful today with modern stressors that we can’t fight or flee, such as work deadlines, Potash adds. Consequently, chronic stress might instead lead to depression or other mood disorders triggered by epigenetic changes.

Potash notes that, eventually, doctors may be able to look for these epigenetic changes in DNA isolated from a patient’s blood to predict or diagnose psychiatric illnesses. Ultimately, researchers may someday be able to target these epigenetic marks with drugs to treat depression and other diseases.

Source: Johns Hopkins Medicine

Eric Bakker ND’s  comment: What this Hopkins study has revealed is something we have known for years – that acute or chronic low grade stress affects our cortisol level, initially the levels will be high and then reduce over time. Dr. James Wilson mentioned in a lecure in New Zealand that cortisol affects every single part of a person’s body, save the fingernails and hair. The mental and emotional state of a person is profoundly affected, and the only current conventional treatments are aimed at pharmaceutical drug intervention. The time has now in the 21st century come for medical scientists to now fully expose the affects of stress on the human organism, and help direct our attention at the altered state of the HPA axis. We know that stress causes disease – it is the archetypal cause. We now need to focus our treatments at the primary exciting causes and stop treating the end effects. Stress causes illness – a fact. Thomas Huxley once said: "The great tragedy of science is the slaying of a beautiful hypothesis by an ugly fact".

 

Diana Parker said,

March 1, 2011 @ 8:12 am

I have had 14 years of hell in the mental health system (losing everything along the way). I agree with your adrenal fatigue theory absolutely. I am now labeled bipolar II because I developed hypomania on certain antidepressants. I am very pleased to have this information as I start to work as a peer support specialist in the mh industry! I now use Omega 3, Vit C, Magnesium & Kelp supplements but will endeavour to obtain a copy of John Wilsons book here in NZ.

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