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TGR5多种配体抑制高脂饮食小鼠肥胖及高血糖的效果对比研究

陈小松 闫柳 陈瑛 李向禹 郭志辉 李铭

中国美容医学2017,Vol.26Issue(7):32-36,5.
中国美容医学2017,Vol.26Issue(7):32-36,5.

TGR5多种配体抑制高脂饮食小鼠肥胖及高血糖的效果对比研究

Comparison of the Effects of TGR5 Ligands on Obesity and Hyperglycemia in High Fat Diet Mice

陈小松 1闫柳 1陈瑛 1李向禹 1郭志辉 1李铭1

作者信息

  • 1. 福建医科大学附属协和医院整形外科 福建 福州 350001
  • 折叠

摘要

Abstract

Objective To screen out the best ligand by comparing the weight loss and hypoglycemic effects of various ligands for bile acid receptor TGR5 in diet-induced obese mice. Methods Wild-type mice of 6 weeks old were fed with HF or the control regular chow diet for 10 weeks. Then mice fed with HF were randomly divided into seven groups. One group were kept feeding with HF. The other groups were switched to HF+OA(H)、HF+OA(L)、HF+CDCA、HF+CA、HF+DCA、HA+LCA for additional 10 weeks. Glucose tolerance test and serum insulin levels were detected after 20 weeks. Hematoxylin and eosin staining was performed for standard histological examination in liver and adipose tissues. Expression of genes related to glucose metabolism in adipose tissues was measured by Real-time PCR. Mice body weights were monitored during the entire process. Results TGR5 activation by its ligands decreased the body weight, enhanced insulin sensitivity in mice and up-regulated the expression of genes related to fatty acid synthesis and oxidation in adipose tissues, with OA(H), CDCA and CA affected significantly. Conclusion OA(H)、CDCA and CA were identified as being effective at reducing weight, improving glucose tolerance, reducing serum insulin levels, relieving liver lipid deposition and regulating the expression of fat metabolism related genes.

关键词

TGR5配体/褐色脂肪/肥胖/糖脂代谢

Key words

TGR5 ligands/BAT/obesity/glycolipid metabolism

分类

医药卫生

引用本文复制引用

陈小松,闫柳,陈瑛,李向禹,郭志辉,李铭..TGR5多种配体抑制高脂饮食小鼠肥胖及高血糖的效果对比研究[J].中国美容医学,2017,26(7):32-36,5.

基金项目

国家自然科学基金(No.81372092) (No.81372092)

国家自然科学基金(No.81671930) (No.81671930)

福建省科技厅高校产学研合作项目(No.2016Y4003) (No.2016Y4003)

福建省发改委产业技术联合创新项目(No. 02011601) (No. 02011601)

福建省财政专项项目(No.010110002) (No.010110002)

中国美容医学

OACSTPCD

1008-6455

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