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组胺对豚鼠乳头肌细胞内钠离子活性及收缩张力的影响。

Effects of histamine on intracellular Na+ activity and twitch tension in guinea pig papillary muscles.

作者信息

Yang J M, Chu C H, Yang S N, Jao M J

机构信息

Department of Physiology and Biophysics, National Defense Medical Center, Taipei, Taiwan, R.O.C.

出版信息

Jpn J Physiol. 1993;43(2):207-20. doi: 10.2170/jjphysiol.43.207.

Abstract

Effects of histamine on the twitch tension, intracellular Na+ activity (aiNa), and action potential were simultaneously and continuously measured in the isolated cardiac papillary muscle of guinea pigs. In the driven fiber at 60 beats/ min, histamine induced a concentration-dependent positive inotropic effect, and apparently increased the amplitude of the action potential and shortened the duration at 3 microM, and significantly decreased aiNa by 6.7% from the control value of 4.5 +/- 0.1 mM (n = 6, p < 0.05) at 0.3 microM. Cimetidine at 10 microM did not produce any significant effect but partially antagonized the action of histamine. The respective concentrations of 1 and 3 microM histamine significantly decreased aiNa by 5.4 and 14.3% from the control 5.6 +/- 0.1 mM (n = 6, p < 0.05) in the presence of 10 microM cimetidine. Chlorpheniramine at 10 microM significantly reduced the twitch tension and aiNa, and prolonged the action potential duration. Histamine at 1 microM increased the twitch tension and decreased aiNa from 4.5 +/- 0.1 to 4.1 +/- 0.1 mM (n = 5, p < 0.05) in the presence of 10 microM chlorpheniramine. The combined application of 10 microM cimetidine and 10 microM chlorpheniramine reduced the twitch tension and abolished most effects of histamine. In high potassium solution (16.2 mM), 1 microM histamine significantly decreased aiNa by 12.9% from the control of 3.1 +/- 0.2 mM (n = 5, p < 0.05). The treatment of 0.5 or 1 microM ouabain increased the tension development and aiNa, and abolished the decrease in aiNa produced by the effect of histamine. The results suggest that histamine can directly stimulate Na-K pump in sarcolemma through means of the activation of both H1- and H2-receptors.

摘要

在豚鼠离体心脏乳头肌中,同时连续测量组胺对抽搐张力、细胞内钠离子活性(aiNa)和动作电位的影响。在驱动频率为60次/分钟的纤维中,组胺诱导出浓度依赖性正性肌力作用,在3微摩尔时明显增加动作电位幅度并缩短动作电位时程,在0.3微摩尔时使aiNa较4.5±0.1毫摩尔的对照值显著降低6.7%(n = 6,p < 0.05)。10微摩尔的西咪替丁未产生任何显著影响,但部分拮抗组胺的作用。在存在10微摩尔西咪替丁的情况下,1微摩尔和3微摩尔组胺分别使aiNa较5.6±0.1毫摩尔的对照值显著降低5.4%和14.3%(n = 6,p < 0.05)。10微摩尔的氯苯那敏显著降低抽搐张力和aiNa,并延长动作电位时程。在存在10微摩尔氯苯那敏的情况下,1微摩尔组胺增加抽搐张力并使aiNa从4.5±0.1毫摩尔降至4.1±0.1毫摩尔(n = 5,p < 0.05)。联合应用10微摩尔西咪替丁和10微摩尔氯苯那敏降低抽搐张力并消除组胺的大部分作用。在高钾溶液(16.2毫摩尔)中,1微摩尔组胺使aiNa较3.1±0.2毫摩尔的对照值显著降低12.9%(n = 5,p < 0.05)。用0.5或1微摩尔哇巴因处理可增加张力发展和aiNa,并消除组胺作用所导致的aiNa降低。结果表明,组胺可通过激活H1和H2受体直接刺激肌膜上的钠钾泵。

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