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Gene expression related to lipid and glucose metabolism in white adipose tissue.

Authors :
Kadota Y
Kawakami T
Takasaki S
Sato M
Suzuki S
Source :
Obesity research & clinical practice [Obes Res Clin Pract] 2016 Jan-Feb; Vol. 10 (1), pp. 85-93. Date of Electronic Publication: 2015 Jun 05.
Publication Year :
2016

Abstract

Problem: A number of endogenous and external factors influence the development of obesity. However, the factors responsible for these differences in obesity pathogenesis between males and females are largely unknown.<br />Methods: We investigated the expression of 35 genes related to lipid and glucose metabolism and to receptors for insulin signaling in white adipose tissue (WAT) of 8-week-old 129/Sv mice and mice fed standard diet (STD) or high fat diet (HFD) for 35 weeks in males and females.<br />Results: At 8 weeks, the expression levels of two genes for fatty acid synthesis, Acaca and Fasn, were higher in females than in males. Female mice fed a STD for 35 weeks also had higher expression levels of an additional four genes related to glucose transporters (Slc2a1 and Slc2a4) and adipokines (Adipoq and Nampt). The expression levels of these six genes were also higher in females than in males fed a HFD for 35 weeks. At 43 weeks old, the female-to-male expression ratio of these six genes was similar for the STD and HFD groups. Furthermore, glucose tolerance testing showed that the half-life for the elimination of elevated blood glucose was shorter in females than males, although blood glucose parameters were generally similar between females and males.<br />Conclusions: These findings suggest that sex and aging may cause diet-independent differences in gene expression levels in female and male mice, and that higher expression of these genes in females could contribute to higher metabolic activity and resistance to obesity compared with males.<br /> (Copyright © 2015 Asia Oceania Association for the Study of Obesity. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1871-403X
Volume :
10
Issue :
1
Database :
MEDLINE
Journal :
Obesity research & clinical practice
Publication Type :
Academic Journal
Accession number :
25979685
Full Text :
https://doi.org/10.1016/j.orcp.2015.04.009