| Literature DB >> 17141367 |
Charles V Mobbs1, Jason Mastaitis, Kelvin Yen, Joseph Schwartz, Vinuta Mohan, Michal Poplawski, Fumiko Isoda.
Abstract
High-fat diets produce obesity in part because, per calorie, glucose produces greater post-prandial thermogenesis than lipids, an effect probably mediated by glucose-sensing neurons. A very low-carbohydrate/high-fat/high-protein Atkins-type diet produces obesity but is marginally ketogenic in mice. In contrast, high-sucrose/low-fat diets, and very low-carbohydrate/high-fat/low-protein (anti-epileptic) ketogenic diets reverse diet-induced obesity independent of caloric intake. We propose that a non-ketogenic high-fat diet reduces glucose metabolism and signaling in glucose-sensing neurons, thereby reducing post-prandial thermogenesis, and that a ketogenic high-fat diet does not reduce glucose signaling, thereby preventing and/or reversing obesity.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17141367 PMCID: PMC2714161 DOI: 10.1016/j.appet.2006.06.007
Source DB: PubMed Journal: Appetite ISSN: 0195-6663 Impact factor: 3.868