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新型强心剂MCI - 154可逆转酸性pH值引起的心肌肌丝对钙离子反应性的降低:与舒马唑和匹莫苯丹的比较。

MCI-154, a novel cardiotonic agent, reverses the acidic pH-induced decrease in responses of cardiac myofilaments to Ca++: comparison with sulmazole and pimobendan.

作者信息

Kitada Y, Abe Y, Narimatsu A, Tobe A

机构信息

Pharmaceuticals Laboratory, Mitsubishi Kasei Corporation, Yokohama, Japan.

出版信息

J Pharmacol Exp Ther. 1991 May;257(2):812-9.

PMID:2033522
Abstract

In the present study, we have examined the effects of decreasing pH from 7.0 to 6.6 on the tension developed by direct activation of the myofilaments in chemically skinned fibers from guinea pig papillary muscles. We then compared the effects of the novel inotropic agents MCI-154, pimobendan and sulmazole, which have direct action on cardiac myofilaments, on the acidic pH-induced changes in responses of the contractile system to Ca++. The reduction of pH from 7.0 to 6.8 shifted the pCa (-log[Ca++] M)-tension relation curve to the right with no change in maximum tension. However, the reduction of pH from 7.0 to 6.6 shifted the pCa tension relation curve to the right and also depressed maximum force development. These effects were reversible by returning to neutral pH (pH 7.0), but were not overcome by increasing the free [Ca++] (decreasing pCa from 4.4 to 4.0). The amplitude of pMg-ATP (-log[MgATP]M)-tension curve in the absence of free Ca++ (Ca++ less than 1 nM, bell-shaped curve) was shifted downward by reducing pH from 7.0 to 6.6. MCI-154 (1-100 microM) reversed the acidic pH-induced decrease of tension development which was activated by pCa 5.8 in a concentration-dependent manner. Moreover, the acidosis induced reductions of maximum tension (pCa, 4.4) and pMgATP 6.0-activated tension (Ca++ less than 1 nM) were also reversed by MCI-154 (1-100 microM) in a concentration-dependent manner.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,我们检测了将pH从7.0降至6.6对豚鼠乳头肌化学去膜纤维中肌丝直接激活所产生张力的影响。然后,我们比较了新型正性肌力药物MCI-154、匹莫苯丹和舒马唑对酸性pH诱导的收缩系统对Ca++反应变化的影响,这些药物对心肌肌丝有直接作用。将pH从7.0降至6.8时,pCa(-log[Ca++] M)-张力关系曲线右移,最大张力无变化。然而,将pH从7.0降至6.6时,pCa张力关系曲线右移,同时最大力发展也受到抑制。通过恢复到中性pH(pH 7.0),这些效应是可逆的,但增加游离[Ca++](将pCa从4.4降至4.0)并不能克服这些效应。在无游离Ca++(Ca++小于1 nM,钟形曲线)时,将pH从7.0降至6.6会使pMg-ATP(-log[MgATP]M)-张力曲线向下移动。MCI-154(1-100 microM)以浓度依赖的方式逆转了酸性pH诱导的由pCa 5.8激活的张力发展降低。此外,MCI-154(1-100 microM)也以浓度依赖的方式逆转了酸中毒诱导的最大张力(pCa,4.4)和pMgATP 6.0激活的张力(Ca++小于1 nM)降低。(摘要截断于250字)

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