Suppr超能文献

[氨氯地平对离体灌注大鼠心脏缺血后早期和晚期恢复的影响——Na⁺/H⁺和Na⁺/Ca²⁺交换可能的参与情况]

[Effect of amiloride on the early and late stage of postischemic recovery in isolated perfused rat hearts--possible involvement of Na+/H+ and Na+/Ca2+ exchange].

作者信息

Yoshizumi M, Kitagawa T, Masuda Y, Hori T, Kawahito T, Chikugo F, Fukuta Y, Katoh I

机构信息

Department of Cardiovascular Surgery, University of Tokushima, School of Medicine, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1996 Sep;44(9):1735-41.

PMID:8911047
Abstract

To investigate whether Na+/H+ exchange or Na+/Ca2+ exchange involves in the ischemic-reperfusion injury, we examined the effect of amiloride, a potent inhibitor of Na+/H+ exchange, on the ischemic reperfused rat heart. When, the hearts were loaded with 0.1 mM amiloride preischemically, the recovery of left ventricular developed pressure was significantly improved than that of the control group, whereas the recovery of heart rate was not influenced by amiloride pretreatment at 30 min of reperfusion. Measurement of intracellular cations revealed that intracellular Na+ accumulation in the early stage (within 5 min) of reperfusion was inhibited by amiloride pretreatment. On the other hand, in the late stage (from 5 min to 30 min) of reperfusion, Ca2+ overload was inhibited by amiloride. These results suggest that Na+/H+ exchange mainly participates in the early stage of reperfusion injury and Na+/Ca2+ exchange system, secondary to the Na+/H+ exchange, participates in the late stage of the reperfusion injury. Moreover, pretreatment with amiloride also decreased creatine phosphokinase activity in the coronary effluent and completely abolished the incidence of ventricular arrhythmia during reperfusion. It is assumed that the improvement of postischemic cardiac dysfunction induced by amiloride pretreatment may be attributable to its inhibition on the resultant Ca2+ accumulation during ischemia.

摘要

为了研究钠/氢交换或钠/钙交换是否参与缺血再灌注损伤,我们检测了钠/氢交换的强效抑制剂氨氯地平对缺血再灌注大鼠心脏的影响。当心脏在缺血前加载0.1 mM氨氯地平时,左心室舒张末压的恢复较对照组显著改善,而在再灌注30分钟时,心率的恢复不受氨氯地平预处理的影响。细胞内阳离子的测定显示,氨氯地平预处理可抑制再灌注早期(5分钟内)细胞内钠的蓄积。另一方面,在再灌注后期(5分钟至30分钟),氨氯地平可抑制钙超载。这些结果表明,钠/氢交换主要参与再灌注损伤的早期,而继发于钠/氢交换的钠/钙交换系统参与再灌注损伤的后期。此外,氨氯地平预处理还降低了冠状动脉流出液中肌酸磷酸激酶的活性,并完全消除了再灌注期间室性心律失常的发生率。推测氨氯地平预处理诱导的缺血后心脏功能障碍的改善可能归因于其对缺血期间所致钙蓄积的抑制作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验