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多巴胺对豚鼠心脏标本跨膜电位的影响。

Effect of dopamine on the transmembrane potentials of guinea-pig heart preparations.

作者信息

Kecskeméti V, Kelemen K

出版信息

Pol J Pharmacol Pharm. 1985 May-Jun;37(3):411-9.

PMID:2415959
Abstract

The effects of dopamine on the transmembrane action potentials of electrically driven left auricle and right papillary muscle of guinea pig were studied in Tyrode solution and in 25 mM K+-Tyrode solution. Under physiological condition dopamine at concentration less than 10(-6) M had no effect, at concentrations between 10(-6) and 10(-4) M it slightly increased the resting potential (RP), caused a marked increase of the overshoot (OS), but did not change the maximum rate of rise (Vmax) of the action potential (AP). The duration of AP was significantly enhanced by 10(-6) and 10(-5) M but was shortened by 10(-4) M dopamine. The effects of dopamine on AP were antagonized by pindolol (4 X 10(-7) M) but not by phentolamine (5 X 10(-6) M). In the atrium in which the fast sodium channels were blocked by partial depolarization (25 mM K+-Tyrode) and the preparation was inexcitable, dopamine in high concentrations (10(-4)--2.5 X 10(-4) M) restored the electrical and mechanical activity. Dopamine induced APs having very slow rate of rise and low RP, characteristics of the given extracellular K+ concentration. The slow electrical responses were unaffected by haloperidol (10(-5) M), but were abolished by pindolol. The effects of dopamine and adrenaline on the depressed fast Na+ system (using 4 mM to 20 mM K+-Tyrode solution) were compared in the papillary muscle. The steady state inactivation of Vmax was shifted by 6 mV to more negative potentials by adrenaline (5 X 10(-6) M) and by 3 mV to more negative potentials by dopamine (2.5 X 10(-4) M).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在台氏液和25 mM钾 - 台氏液中研究了多巴胺对豚鼠电驱动左心房和右乳头肌跨膜动作电位的影响。在生理条件下,浓度低于10(-6) M的多巴胺无作用,浓度在10(-6)至10(-4) M之间时,它会轻微增加静息电位(RP),使超射(OS)显著增加,但不改变动作电位(AP)的最大上升速率(Vmax)。10(-6) M和10(-5) M的多巴胺可显著延长AP的持续时间,但10(-4) M的多巴胺则使其缩短。多巴胺对AP的作用可被吲哚洛尔(4×10(-7) M)拮抗,但不能被酚妥拉明(5×10(-6) M)拮抗。在快速钠通道因部分去极化(25 mM钾 - 台氏液)而被阻断且标本无兴奋性的心房中,高浓度(10(-4) - 2.5×10(-4) M)的多巴胺可恢复电活动和机械活动。多巴胺诱导的AP上升速率非常缓慢且RP较低,具有给定细胞外钾浓度的特征。缓慢的电反应不受氟哌啶醇(10(-5) M)影响,但可被吲哚洛尔消除。在乳头肌中比较了多巴胺和肾上腺素对抑制的快速钠系统(使用4 mM至20 mM钾 - 台氏液)的作用。肾上腺素(5×10(-6) M)使Vmax的稳态失活向更负电位偏移6 mV,多巴胺(2.5×10(-4) M)使其向更负电位偏移3 mV。(摘要截短于250字)

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