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Home NEWS Science News Health

Does dietary restriction protect against age-related leaky gut?

Bioengineer by Bioengineer
November 5, 2018
in Health
Reading Time: 3 mins read
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Flies eating a Spartan diet are protected from leaky gut and the systemic inflammation associated with it as they age. Conversely, flies on a rich Atkins-like diet are more prone to developing intestinal permeability, a condition linked to a variety of human conditions including inflammatory bowel disease. Publishing in PLOS Genetics, researchers from the Kapahi lab at the Buck Institute show that gaps in the intestinal barrier are caused by an age-related increase in the death of intestinal epithelial cells, also known as enterocytes.

"The integrity of our gut declines with age and problems with intestinal permeability are now suspect in chronic inflammation, metabolic diseases and even neurological diseases like Alzheimer's," said Buck professor Pankaj Kapahi, senior scientist on the study. "The possibility that dietary restriction, or the use of dietary restriction mimetics, could help prevent this decline in humans opens a new area of research that could influence healthspan and longevity."

Lead scientist Kazutaka Akagi, a former postdoc in the Kapahi lab who now runs his own lab at the National Center for Geriatrics and Gerontology in Aichi, Japan, zeroed in on dMyc, a gene involved in cell proliferation. He observed that levels of dMyc act as a barometer of cellular fitness in enterocytes, post-mitotic intestinal cells. He found that cells that have too little dMyc get eliminated by neighboring cells through a process termed "cell competition" in an attempt to maintain gut health. "But levels of dMyc naturally decline with age in enterocytes, leading to excessive cell loss and thus a leaky gut," he said. "In our study, this decline in dMyc was enhanced by the rich diet, while dietary restriction maintained dMyc level in the flies, preventing leaky gut and extending the lifespan of the animals."

Researchers in the Kapahi lab also looked at the role of dysbiosis, an imbalance in the intestinal bacteria or microbiome of the flies, as a potential contributor to leaky gut. Even though dysbiosis has been proposed as a leading cause of leaky gut, researchers found that removing intestinal bacteria with antibiotics conferred only minimal protection to the animals and did not prevent age-related damage to enterocytes. "The intestinal epithelium is affected by everything that moves through the gut. It would make sense that diet would have major impact on the health of those cells, especially over a lifetime of eating," said Kapahi. "While we understand the interest in the role of the microbiome, we think that diet may ultimately be the primary driver in cellular changes leading to leaky gut."

###

Citation: Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster.

DOI: 10.1371/journal.pgen.1007777

Other Buck researchers involved in the study include Kenneth A. Wilson, Subhash D. Katewa, Mauricio Ortega, Jesse Simons, Tyler Hilsabeck, Subir Kapuria, Amit Sharma and Heinrich Jasper.

The work was funded by NIH grants R01AG038688 and R01AG045835 and grants from the American Federation of Aging Research and the Hillblom Foundation.

About the Buck Institute for Research on Aging

At the Buck, we aim to end the threat of age-related diseases for this and future generations. We bring together the most capable and passionate scientists from a broad range of disciplines to study mechanisms of aging and to identify therapeutics that slow down aging. Our goal is to increase human health span, or the healthy years of life. Located just north of San Francisco, we are globally recognized as the pioneer and leader in efforts to target aging, the number one risk factor for serious diseases including Alzheimer's, Parkinson's, cancer, macular degeneration, heart disease, and diabetes. The Buck wants to help people live better longer. Our success will ultimately change healthcare. Learn more at: https://buckinstitute.org

Media Contact

Kris Rebillot
[email protected]
415-209-2080
@BuckInstitute

http://www.buckinstitute.org

http://dx.doi.org/10.1371/journal.pgen.1007777

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