Protective effects of calcium antagonist (nitrendipine) on calcium ionophore A23187-induced liver cell injury.

S Matsuda
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Abstract

Calcium ionophore A23187-induced liver damage was studied in perfused rat liver and isolated hepatocytes. Two groups of calcium antagonists, dihydropyridine-type and nondihydropyridine-type, were examined for their protective effects on A23187-induced liver damage. The former calcium antagonist inhibited cell damage at pharmacological doses, whereas nondihydropyridine-type calcium antagonists were unable to prevent A23187-induced cytotoxicity. Different inhibitors, such as cAMP phosphodiesterase inhibitor OPC3689, calmodulin inhibitor W-7, and C-kinase inhibitor H-7, were tested in isolated hepatocytes to determine whether intracellular signal transduction systems are involved in the liver cell injury produced by A23187. Calcium ionophore A23187-induced LDH activity of the medium was depressed by W-7 and H-7 to 55 +/- 4% and 63 +/- 4% of controls (p less than 0.01), respectively. However, OPC3689 did not show a protective effect. We conclude that A23187-induced liver cell injury was inhibited by dihydropyridine-type calcium antagonists which may interfere with activation of calmodulin and C-kinase.

钙拮抗剂尼群地平对钙离子载体a23187诱导的肝细胞损伤的保护作用。
研究了钙离子载体a23187对灌注大鼠肝脏和离体肝细胞的损伤作用。研究了两组钙拮抗剂(二氢吡啶型和非二氢吡啶型)对a23187肝损伤的保护作用。前一种钙拮抗剂在药理学剂量下抑制细胞损伤,而非二氢吡啶型钙拮抗剂无法阻止a23187诱导的细胞毒性。不同的抑制剂,如cAMP磷酸二酯酶抑制剂OPC3689,钙调素抑制剂W-7和c激酶抑制剂H-7,在分离的肝细胞中进行了测试,以确定细胞内信号转导系统是否参与了A23187引起的肝细胞损伤。W-7和H-7对钙离子载体a23187诱导的LDH活性的抑制作用分别为对照的55 +/- 4%和63 +/- 4% (p < 0.01)。然而,OPC3689没有显示出保护作用。我们认为,二氢吡啶型钙拮抗剂可以抑制a23187诱导的肝细胞损伤,这种拮抗剂可能干扰钙调素和c激酶的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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