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钙拮抗剂对成年大鼠心室肌细胞活力的不同影响。

Differential effects of calcium antagonists on viability of adult rat ventricular myocytes.

作者信息

Miller L S, Barrett J N, Cameron J S, Bassett A L

出版信息

J Mol Cell Cardiol. 1985 Dec;17(12):1129-37. doi: 10.1016/s0022-2828(85)80109-7.

DOI:10.1016/s0022-2828(85)80109-7
PMID:4087303
Abstract

This study was designed to determine whether the various classes of Ca2+ channel blockers have differential protective effects on isolated adult rat ventricular myocytes exposed to high K+ under anoxic (100% N2) conditions. Calcium-tolerant myocytes were incubated under control (4mM K+) aerobic conditions and then subjected to high K+ (75 mM) and N2. The cells were assessed by morphological criteria (i.e. absence of blebbing, granulation etc.), maintenance of ATP levels, exclusion of trypan blue, and the presence or absence of spontaneous contractile activity. Under control conditions, the cells were quiescent and declined at a rate of approximately 10%/h. In the absence of O2, the rate of cell decline was significantly faster. Verapamil, diltiazem and the dihydropyridines had no significant effects on cell decline under these conditions. Cells exposed to 75 mM K0+ exhibited contractile activity and accelerated rate of decline under anoxic conditions; these effects were independent of lowering Na0+ to 75mM. Cells in high K0+ and N2 were significantly protected (i.e. contractile activity and rate of decline were decreased) by verapamil, less so by diltiazem, and not at all by the dihydropyridines. The uptake of 45Ca2+ into cells in high K0+ was not significantly altered by verapamil or diltiazem. Caffeine induced the immediate cessation of contractile activity of cells incubated in high K0+, but did not affect the accelerated rate of cell declined under anoxic conditions. Verapamil and diltiazem still conferred significant protection in this non-beating cell preparation. Neither verapamil nor diltiazem had any effect on the oscillation frequency of skinned heart cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在确定各类钙通道阻滞剂对在缺氧(100%氮气)条件下暴露于高钾环境的成年大鼠离体心室肌细胞是否具有不同的保护作用。耐钙心肌细胞先在对照(4mM钾)有氧条件下孵育,然后置于高钾(75mM)和氮气环境中。通过形态学标准(即无起泡、颗粒化等)、ATP水平的维持、台盼蓝排斥试验以及有无自发收缩活动来评估细胞。在对照条件下,细胞静止,以约10%/小时的速率衰退。在无氧条件下,细胞衰退速率明显加快。维拉帕米、地尔硫䓬和二氢吡啶类药物在这些条件下对细胞衰退无显著影响。暴露于75mM钾的细胞在缺氧条件下表现出收缩活动且衰退速率加快;这些作用与将钠离子降至75mM无关。高钾和氮气环境中的细胞受到维拉帕米的显著保护(即收缩活动和衰退速率降低),地尔硫䓬的保护作用较小,而二氢吡啶类药物则完全没有保护作用。维拉帕米或地尔硫䓬对高钾环境中细胞摄取45Ca2+没有显著影响。咖啡因可使高钾环境中孵育的细胞立即停止收缩活动,但不影响缺氧条件下细胞加快的衰退速率。在这种无搏动细胞制剂中,维拉帕米和地尔硫䓬仍具有显著保护作用。维拉帕米和地尔硫䓬对去表皮心肌细胞的振荡频率均无影响。(摘要截断于250字)

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引用本文的文献

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Effects of hypoxia, elevated K+ and acidosis on the potency of verapamil, diltiazem and nifedipine in the guinea-pig isolated papillary muscle.缺氧、高钾血症和酸中毒对豚鼠离体乳头肌中维拉帕米、地尔硫䓬和硝苯地平效能的影响。
Br J Pharmacol. 1989 Nov;98(3):937-49. doi: 10.1111/j.1476-5381.1989.tb14624.x.