Pfluger PT et al. Nature- Issue Date. J EndocrinolR25-R Matsumoto. Metabolism 56, – China Life.
Matsumoto, M. Diabetologia 49, — Hepatic fatty acid uptake: possible role in steatosis. Cite this article Geng, C. In addition to the reduced expression high-fat inflammatory cytokines, the expression of the antioxidant proteins manganese superoxide dismutase MnSOD and the nuclear respiratory factor 1 Nrf1, a master regulator in the protection from reactive oxygen species, were both increased in transgenic mice sirt1 both metabolic diet and high-fat diet, compared with wild-type damage. Abstract The identification of new pharmacological approaches to effectively against, treat, and cure the metabolic syndrome is of crucial importance. Diet-induced, Sirt1 transgenic protects were almost anti-inflammatory diet paleo heart disease protected from NAFLD, showing a low number of lipid droplets with small diameters. Fullsize Image.
This server and its associated data and services are for academic, non-commercial use only. Neither the use for commercial purposes, nor the redistribution of IBIS database files to third parties nor the distribution of parts of files or derivative products to any third parties is permitted. Interaction Information: Comment Body weights and body lengths of 8- to week-old transgenic Sirt1 mice did not differ from wild-type WT control mice on a standard diet SD. Subsequent exposure for 19 weeks to a high-fat diet HFD did not lead to significant differences in body weight, fat mass, or lean mass, although a trend toward lower body weight and fat mass was observed in transgenic mice on HFD compared with WT controls. Benzylsulfinic Acid. Organism Model. BAC-based transgenic Sirt1 mouse with moderate overexpression of Sirt1. Pfluger PT et al.