The headline and pitch of this study seem misleading. Fasting for 24 hours in mice is not the same as fasting for 24 hours in humans. We'd have to fast for a much longer period of time to gain the benefits (if any...) suggested here. They're looking for a fasting mimetic, of course, because of their well-traveled belief that "people won't fast because it's too hard or too dangerous..." I beg to differ. More people would be motivated to fast if more studies in actual humans were performed that indicate fasting might actually do important things to slow metabolic aging.
Nevertheless, it's nice to see something being done on fasting; but I wish Sabatini et al would study fasting in humans.
Fasting For Just 24 Hours Boosts The Regeneration of Stem Cells, Study Finds
PETER DOCKRILL 7 MAY 2018
https://www.sciencea...stine-longevity
Fasting Activates Fatty Acid Oxidation to Enhance Intestinal Stem Cell Function during Homeostasis and Aging
Cell Stem Cell Volume 22, Issue 5, p769–778.e4, 3 May 2018
Highlights
•Fasting induces fatty acid oxidation (FAO) in intestinal stem and progenitor cells
•Aging reduces ISC numbers and function, correlating with decreased FAO
•PPAR/CPT1a-mediated FAO augments ISC function in aging and during regeneration
•PPARδ agonists boost and restore ISC and progenitor function in young and old age
Summary
Diet has a profound effect on tissue regeneration in diverse organisms, and low caloric states such as intermittent fasting have beneficial effects on organismal health and age-associated loss of tissue function. The role of adult stem and progenitor cells in responding to short-term fasting and whether such responses improve regeneration are not well studied. Here we show that a 24 hr fast augments intestinal stem cell (ISC) function in young and aged mice by inducing a fatty acid oxidation (FAO) program and that pharmacological activation of this program mimics many effects of fasting. Acute genetic disruption of Cpt1a, the rate-limiting enzyme in FAO, abrogates ISC-enhancing effects of fasting, but long-term Cpt1a deletion decreases ISC numbers and function, implicating a role for FAO in ISC maintenance. These findings highlight a role for FAO in mediating pro-regenerative effects of fasting in intestinal biology, and they may represent a viable strategy for enhancing intestinal regeneration.