Galanin antagonist increases insulin resistance by reducing glucose transporter 4 effect in adipocytes of rats

被引:56
作者
Guo, Lili [2 ]
Shi, Mingyi [1 ]
Zhang, Ling [1 ]
Li, Guangzhi [1 ]
Zhang, Lingxiang [1 ]
Shao, Hu [1 ]
Fang, Penghua [1 ]
Ma, Yingping [1 ]
Li, Jian [1 ]
Shi, Qiaojia [1 ]
Sui, Yumei [1 ]
机构
[1] Yangzhou Univ, Dept Physiol, Yangzhou 225001, Jiangsu Prov, Peoples R China
[2] Chuzhou Coll, Dept Phys Educ, Chuzhou 239012, Anhui, Peoples R China
关键词
Adipose; GLUT4; Glucose transport; Galanin; GLUCOSE-TRANSPORT; ADIPOSE-TISSUE; LIPID-METABOLISM; EXPRESSION; INHIBITION; ENDOCRINE; SECRETION; OBESITY; FAMILY; GENE;
D O I
10.1016/j.ygcen.2011.05.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Seeing that galanin increases animal body weight on the conditions of inhibiting insulin secretion and animals with metabolic disorder of galanin easily suffer from diabetes, we postulate that endogenous galanin is necessary to reduce insulin resistance in adipocytes. To test this hypothesis, we compared four groups of rats to examine whether an increase in galanin secretion stimulated by swimming may reduce insulin resistance. The rats from sedentary and trained drug groups were injected by M35, a galanin antagonist. The rats from trained control and trained drug groups swam after each injection for four weeks. We found that exercise significantly elevated plasma galanin contents and glucose transporter 4 (GLUT4) mRNA levels in adipocytes. Meanwhile. M35 treatment reduced GLUT4 and GLUT4 mRNA levels, and glucose infusing rates in euglycemic-hyperinsulinemic clamp tests. The ratios of GLUT4 concentrations at plasma membranes to total cell membranes in both drug groups were lower compared with each control group, respectively. These observations suggest that endogenous galanin reduces insulin resistance by increasing GLUT4 contents and promoting GLUT4 transportation from intracellular membranes to plasma membranes in adipocytes. Galanin is an important hormone to reduce insulin resistance in rats. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:159 / 163
页数:5
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