| Literature DB >> 29129786 |
Rachel J Perry1, Liang Peng2, Gary W Cline1, Yongliang Wang1, Aviva Rabin-Court1, Joongyu D Song1, Dongyan Zhang3, Xian-Man Zhang1, Yuichi Nozaki1, Sylvie Dufour3, Kitt Falk Petersen1, Gerald I Shulman4.
Abstract
Caloric restriction rapidly reverses type 2 diabetes (T2D), but the mechanism(s) of this reversal are poorly understood. Here we show that 3 days of a very-low-calorie diet (VLCD, one-quarter their typical intake) lowered plasma glucose and insulin concentrations in a rat model of T2D without altering body weight. The lower plasma glucose was associated with a 30% reduction in hepatic glucose production resulting from suppression of both gluconeogenesis from pyruvate carboxylase (VPC), explained by a reduction in hepatic acetyl-CoA content, and net hepatic glycogenolysis. In addition, VLCD resulted in reductions in hepatic triglyceride and diacylglycerol content and PKCɛ translocation, associated with improved hepatic insulin sensitivity. Taken together, these data show that there are pleotropic mechanisms by which VLCD reverses hyperglycemia in a rat model of T2D, including reduced DAG-PKCɛ-induced hepatic insulin resistance, reduced hepatic glycogenolysis, and reduced hepatic acetyl-CoA content, PC flux, and gluconeogenesis.Entities:
Keywords: T2D; acetyl-CoA; caloric restriction; gluconeogenesis; glycogenolysis; type 2 diabetes; very low calorie diet; very-low-calorie diet
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Year: 2017 PMID: 29129786 PMCID: PMC5762419 DOI: 10.1016/j.cmet.2017.10.004
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287