Downregulation of K+ channel genes expression in type I diabetic cardiomyopathy

被引:73
作者
Qin, DY
Huang, BY
Deng, LL
El-Adawi, H
Ganguly, K
Sowers, JR
El-Sherif, N
机构
[1] New York Harbor Healthcare Syst, Dept Vet Affairs, Brooklyn, NY 11209 USA
[2] Suny Downstate Med Ctr, Dept Med, Brooklyn, NY 11203 USA
关键词
rats; experimental diabetes mellitus; ion channels; gene expression; Kv2.1; Kv4.2; Kv4.3; Ito-f; Ito-g;
D O I
10.1006/bbrc.2001.4825
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
Type I diabetic cardiomyopathy has consistently been shown to be associated with decrease of repolarising K+ currents, but the mechanisms responsible for the decrease are not well defined. We investigated the streptozotocin (STZ) rat model of type I diabetes. We utilized RNase protection assay and Western blot analysis to investigate the message expression and protein density of key cardiac K+ channel genes in the diabetic rat left ventricular (LV) myocytes, Our results show that message and protein density of Kv2.1, Kv4.2, and Kv4.3 are significantly decreased as early as 14 days following induction of type I diabetes in the rat. The results demonstrate, for the first time, that insulin-deficient type I diabetes is associated with early downregulation of the expression of key cardiac K+ channel genes that could account for the depression of cardiac K+ currents, Ito-f and Ito-8. These represent the main electrophysiological abnormality in diabetic cardiomyopathy and is known to enhance the arrhythmogenecity of the diabetic heart. The findings also extend the extensive list of gene expression regulation by insulin. (C) 2001 Academic Press.
引用
收藏
页码:549 / 553
页数:5
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