Defective phosphatidic acid-phospholipase C signaling in diabetic cardiomyopathy

被引:12
作者
Tappia, PS
Maddaford, TG
Hurtado, C
Dibrov, E
Austria, JA
Sahi, N
Panagia, V
Pierce, GN
机构
[1] Univ Manitoba, Fac Pharm, Winnipeg, MB, Canada
[2] St Boniface Gen Hosp, Res Ctr, Inst Cardiovasc Sci, Winnipeg, MB, Canada
[3] Univ Manitoba, Fac Human Ecol, Dept Human Nutr Sci, Winnipeg, MB, Canada
基金
加拿大健康研究院;
关键词
phosphatidic acid; phospholipase C; diabetic cardiomyopathy; cardiomyocyte; calcium transients; heart;
D O I
10.1016/j.bbrc.2004.02.045
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
The effects of exogenous phosphatidic acid (PA) on Ca(2+) transients and contractile activity were studied in cardiomyocytes isolated from chronic streptozotocin-induced diabetic rats. In control cells, 25 muM PA induced a significant increase in active cell shortening and Ca(2+) transients. PA increased IP(3) generation in the control cardiomyocytes and its inotropic effects were blocked by a phospholipase C inhibitor. In cardiomyocytes from diabetic rats, PA induced a 25% decrease in active cell shortening and no significant effect on Ca(2+) transients. Basal and PA-induced IP(3) generation in diabetic rat cardiomyocytes was 3-fold lower as compared to control cells. Sarcolemmal membrane PLC activity was impaired. Insulin treatment of the diabetic animals resulted in a partial recovery of PA responses. Our results, therefore, identify an important defect in the PA-PLC signaling pathway in diabetic rat cardiomyocytes, which may have significant implications for heart dysfunction during diabetes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:280 / 289
页数:10
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