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乙酰毒毛旋花子苷对心室肌变力作用的机电研究。

Electromechanical studies on the inotropic effects of acetylstrophanthidin in ventricular muscle.

作者信息

Greenspan A M, Morad M

出版信息

J Physiol. 1975 Dec;253(2):357-84. doi: 10.1113/jphysiol.1975.sp011194.

Abstract

Three phases in the inotropic response of acetyl strophanthidin (AcS) on the electromechnical activity of the frog ventricular myocardium were identified and studied using a single sucrose voltage-clamp technique and other conventional electrophysiological methods. 2. the positive inotropic response of the drug was accompanied by a shift in tension-voltage relation, so that more tension developed with every depolarization step above the mechanical threshold (-50mV). Only at higher drug concentrations or with long exposure times did the mechanical threshold shift to more negative membrane potentials (-60 to-70 mV). 3. In tetrodotoxin-treated muscles AcS produced marked potentiation of twitch tension and an appropriate shift in the tension-voltage relation. 4. the positive inotropic response of the drug was not related to the magnitude of the direction of the fast or slow Na current. 5. in tetrodotoxin-treated ventricular strips the direction or the magnitude of the secondary inward current (ICa or INa) were not related to the inotropic effect of AcS. 6. AcS shortens the action potential markedly during the later stages of its positive inotropic response. When Ca2+ is omitted from the bathing solution AcS not only fails to shorten the action potential, but often prolongs it. 7. The shortening of the action potential in the presence of AcS is accompanied by an increase in the "instantaneous" membrane conductance both at rest and during the time course of the plateau. 8. The decline in the positive inotropic response of the drug was accompanied by the shortening of the action potential. Electrical or chemical prolongation of the action potential restored the full positive inotropic response if the membrane had not depolarized. 9. Membrane depolarization and the development of diastolic tension always occurred at later stages of drug action. Elevation of [Mg+2]degrees to 5 or 10 mM prevented or suppressed the membrane depolarization and the diastolic tension. 10. KCl-induced contractures were potentiated throughout the duration of drug exposure. The tonic component of the contracture tension was markedly elevated especially at later stages of drug action. 11. The experimental evidence suggests that no unitary mechanism could account for multiple actions of acetyl strophanthidin. However, the contributions of the Na pump, the Ca+2 sequestering system, and the K-efflux system to the various stages of drug action are discussed.

摘要

采用单蔗糖电压钳技术和其他传统电生理方法,确定并研究了乙酰毒毛花苷(AcS)对蛙心室肌机电活动变力反应的三个阶段。2. 药物的正性变力反应伴随着张力 - 电压关系的改变,使得在高于机械阈值(-50mV)的每个去极化步骤中产生更多的张力。只有在较高药物浓度或长时间暴露时,机械阈值才会向更负的膜电位(-60至 -70mV)移动。3. 在河豚毒素处理的肌肉中,AcS使抽搐张力显著增强,并使张力 - 电压关系发生适当改变。4. 药物的正性变力反应与快或慢钠电流的大小或方向无关。5. 在河豚毒素处理的心室条带中,二次内向电流(ICa或INa)的方向或大小与AcS的变力作用无关。6. AcS在其正性变力反应的后期显著缩短动作电位。当从浴液中去除Ca2+时,AcS不仅不能缩短动作电位,反而常常使其延长。7. 在存在AcS的情况下动作电位的缩短伴随着静息时和平台期过程中“瞬时”膜电导的增加。8. 药物正性变力反应的下降伴随着动作电位的缩短。如果膜未去极化,电或化学方式延长动作电位可恢复完全的正性变力反应。9. 膜去极化和舒张期张力的发展总是发生在药物作用的后期。将[Mg+2]°升高至5或10 mM可预防或抑制膜去极化和舒张期张力。10. 在药物暴露的整个过程中,KCl诱导的挛缩增强。挛缩张力的强直成分显著升高,尤其是在药物作用的后期。11. 实验证据表明,没有单一机制可以解释乙酰毒毛花苷的多种作用。然而,讨论了钠泵、Ca+2 螯合系统和钾外流系统对药物作用各个阶段的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3148/1348510/297154b8e8c9/jphysiol00876-0053-a.jpg

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