martes, 13 de enero de 2015

Pathways Underlying the Benefits of Calorie Restriction - NIH Research Matters - National Institutes of Health (NIH)

Pathways Underlying the Benefits of Calorie Restriction - NIH Research Matters - National Institutes of Health (NIH)



National Institutes of Health (NIH) - Turning Discovery Into Health

Contact Us

Mailing Address:
NIH Research Matters
Bldg. 31, Rm. 5B64A, MSC 2094
Bethesda, MD 20892-2094

About NIH Research Matters

Editor: Harrison Wein, Ph.D.
Assistant Editors: Vicki Contie, Carol Torgan, Ph.D.
NIH Research Matters is a weekly update of NIH research highlights from the Office of Communications and Public Liaison, Office of the Director, National Institutes of Health.
ISSN 2375-9593


Pathways Underlying the Benefits of Calorie Restriction

At a Glance

  • A mouse study revealed that some of the health benefits of calorie restriction are due to increased production of the gas hydrogen sulfide.
  • The key metabolic pathways exist in yeast, worms, flies, and mice, suggesting they are highly conserved and could have potential clinical applications.
Calorie restriction is the process of reducing food intake—typically by at least 30% from a normal diet—without malnutrition. Researchers have known since the 1930’s that this regimen, also referred to as dietary restriction, has numerous health benefits. It can extend the lifespan of yeast, worms, flies, and some mice. Calorie restriction can also improve tolerance to certain metabolic stresses to the body.
Hydrogen sulfide molecules.
Calorie restriction leads to increased production of the gas hydrogen sulfide.
A team led by Drs. Christopher Hine and James Mitchell at the Harvard School of Public Health set out to determine the molecular mechanisms by which calorie restriction can bring health benefits. The study was funded in part by NIH’s National Institute on Aging (NIA), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), and National Cancer Institute (NCI). Results appeared online on December 23, 2014, in Cell.
The researchers induced surgical stress in mice by temporarily halting blood flow to the liver. When blood flow is restored to the tissue, it shows damage and inflammation. This injury model, known as ischemia reperfusion, is similar to what occurs during organ transplantation, stroke, or heart attack in humans.
The team found that mice that had their diet restricted by 50% for a week before the surgery showed less liver damage than mice provided with unlimited food. The beneficial effects of the calorie restriction could be blocked, however, by providing the mice with extra methionine and cysteine. These 2 amino acids are notable because they both contain sulfur.
The scientists determined that restricting these 2 sulfur-containing amino acids activated a metabolic pathway called the transsulfuration pathway, which resulted in increased production of the gas hydrogen sulfide (H2S). When they deleted a gene for an H2S-producing enzyme in mice, the protective effects of dietary restriction were lost. Conversely, mice genetically manipulated to make more of the gas had less surgical damage, even without dietary intervention. Thus, production of the gas was important for the benefits of calorie restriction against surgical stress.
Further experiments showed that H2S production played a role in calorie-restricted models of longevity in yeast, worms, fruit flies, and mice. This implicates an evolutionarily conserved metabolic pathway in several of the benefits of calorie restriction.
“This finding suggests that H2S is one of the key molecules responsible for the benefits of dietary restriction in mammals and lower organisms as well,” Mitchell says. “While more experiments are required to understand how H2S exerts its beneficial effects, it does give us a new perspective on which molecular players to target therapeutically in our efforts to combat human disease and aging.”
—by Carol Torgan, Ph.D.

RELATED LINKS:

Reference: Endogenous Hydrogen Sulfide Production Is Essential for Dietary Restriction Benefits. Hine C, Harputlugil E, Zhang Y, Ruckenstuhl C, Lee BC, Brace L, Longchamp A, Treviño-Villarreal JH, Mejia P, Ozaki CK, Wang R, Gladyshev VN, Madeo F, Mair WB, Mitchell JR. Cell. 2014 Dec 23. pii: S0092-8674(14)01525-6. doi: 10.1016/j.cell.2014.11.048. [Epub ahead of print]. PMID: 25542313.
Funding: NIH’s National Institute on Aging (NIA), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), and National Cancer Institute (NCI); Glenn Foundation; Austrian Science Fund; American Heart Association; and the Canadian Institutes of Health Research.

No hay comentarios:

Publicar un comentario