Thursday, December 31, 2009

Acute Stress Leaves Epigenetic Marks on the Hippocampus

Yesterday I posted two long articles of PTSD (PTSD and the Military and The Science of PSTD and its Future as a DSM-V Diagnosis), and in the second, in talking about the science, I mentioned that one of the features is shrinking of hippocampus while the amygdala tends to enlarge.

So, of course, today Science Daily posts an article on new research that shows the impact of acute stress on the hippocampus is mediated by epigenetics. It's interesting that a single 30-minute exposure caused such drastic changes, and more so that the brains did not adapt to the stress over a 21-day period of chronic stress.

And once again, anti-depressants like Prozac (fluoxetine) show an ability to mitigate the damage not through serotonin channels, as the drug companies have promoted, but through reversing some of the methylation effects caused by chronic stress.

Other studies have shown fluoxetine's ability (paroxetine [paxil] appears to do the same thing, in PTSD specifically) to generate neurogenesis in the hippocampus. The mounting evidence that these drugs are effective pieces of the treatment puzzle, but also that they appear to increase hippocampal volume in non-PTSD brains suggests a possible prophylactic use for those who are going into acute or chronic stress situations.

Acute Stress Leaves Epigenetic Marks on the Hippocampus

ScienceDaily (Dec. 31, 2009) — In trying to explain psychiatric disorders, genes simply cannot tell the whole story. The real answers are in the interaction of genes and the environment. Post-traumatic stress disorder requires some trauma, for instance, and people, for the most part, aren't born depressed. Now research has revealed one mechanism by which a stressful experience changes the way that genes are expressed in the rat brain. The discovery of "epigenetic" regulation of genes in the brain is helping change the way scientists think about psychiatric disorders and could open new avenues to treatment.

Richard Hunter, a postdoc in Rockefeller University's Harold and Margaret Milliken Hatch Laboratory of Neuroendocrinology, found that a single 30-minute episode of acute stress causes a rapid chemical change in DNA packaging proteins called histones in the rat hippocampus, which is a brain region known to be especially susceptible to the effects of stress in both rodents and humans.

The chemical change Hunter examined, called methylation, can either increase or decrease the expression of genes that are packaged by the histones, depending on the location of the methylation. He looked for methylation on three regions of histone H3 that have been shown to actively regulate gene expression. In experiments published this month in Proceedings of the National Academy of Sciences, he shows that methylation of one mark, H3K9 trimethyl, roughly doubled in the hippocampus. Methylation of a second mark, H3K27 trimethyl, dropped by about 50 percent in the same area. Changes associated with the third mark were minor.

"The hippocampus is involved in episodic memory, so you would expect it to be sensitive to episodic experiments like this, more so than the motor regions, for instance," says Hunter, who worked on the project with Rockefeller scientists Bruce S. McEwen and Donald W. Pfaff. "But what is surprising is the magnitude and regional specificity of these patterns." The sheer size of the change in histone methylation suggests that it is important to the brain's response to acute stress, although its exact role remains a mystery. The two methyl marks that changed are both thought to repress gene expression usually, but methylation increased in one and decreased in the other.

Hunter also checked for similar changes as a result of chronic stress -- exposure to a 30-minute stress each day for 21 days. He did not find a major effect, which could reflect the animals' adjusting to the stress. However, when he treated the rats with fluoxetine, the generic form of the popular antidepressant Prozac, he reversed some methylation effects associated with chronic stress.

It's becoming increasingly evident, Hunter says, that the epigenetic changes like the methyl marks he observed and others, such as acetylation and phosphorylation, could play a significant role in the brain's response to stress and the treatment of stress related diseases, such as post-traumatic stress disorder.

"There was a thought that the genome project would reveal all in neuropsychiatric disease, but that has proven not to be the case," he says. "Epigenetics has become much more interesting because it allows us to look at how gene expression is changed by environmental events, explainable in part by histone modifications."

Journal Reference:

  1. Hunter et al. Regulation of hippocampal H3 histone methylation by acute and chronic stress. Proceedings of the National Academy of Sciences, 2009; 106 (49): 20912 DOI: 10.1073/pnas.0911143106


Ana said...

Hi William,
I just saw one of your comments at FS.
I'm sorry but you have so many ads at your page that I believe some people reads the ads and don't pay attention to your own work.
I was trapped by this ad:

This is not you.
Sorry to say that.
I know you are a very bright person and that's why I want to tell you this.
Happy New year!

william harryman said...

Sorry you got side-tracked by the ad - I only promote books and that one program run by a couple of friends.

I think it might the "roll over" link function. I'll try to remove that.

Thanks for reading and commenting.