GSK3 involvement in amylin signaling in isolated rat soleus muscle

被引:3
作者
Abaffy, T
Cooper, GJS
机构
[1] Univ Auckland, Fac Sci, Sch Biol Sci, Auckland 1001, New Zealand
[2] Univ Miami, Sch Med, Dept Cellular & Mol Pharmacol, Miami, FL 33136 USA
关键词
glycogen; cAMP; 2-deoxy-glucose; CGRP;
D O I
10.1016/j.peptides.2004.08.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amylin can evoke insulin resistance by antagonizing insulin in a non-competitive manner. Here. we investigated the glycogenolytic effect of amylin in isolated skeletal muscle and compared it to the effects of a calcitonin gene-related peptide (CGRP). Amylin alone had no statistically significant effect on glucose transport. However, amylin decreased insulin-stimulated glucose transport by about 30%. The involvement of cAMP could not be detected at the concentrations shown to promote glycogenolysis. Previously. it has been shown that increased glycogen synthase kinase 3 (GSK3) activity plays a role in insulin resistance. Here. the ratio of GSK3 alpha:beta isoforms in rat soleus was found to be 1:2:1. We found that amylin increased GSK3alpha activity, which in turn led to increased phosphorylation Of glycogen synthase and decreased glycogen synthesis de novo. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:2119 / 2125
页数:7
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