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组胺对犬心脏的变时性和变传导性作用。

Chronotropic and dromotropic effects of histamine on the canine heart.

作者信息

Hageman G R, Urthaler F, Isobe J H, James T N

出版信息

Chest. 1979 May;75(5):597-604. doi: 10.1378/chest.75.5.597.

DOI:10.1378/chest.75.5.597
PMID:436489
Abstract

The actions of 2-methylhistamine (H1 agonists), 4-methylhistamine (H2 agonist), and histamine were studied by selective perfusion of the sinus node artery and atrioventricular node artery in 75 dogs anesthetized with pentobarbital sodium. 2-Methylhistamine and histamine had variable and inconsistent effects on the sinus rate. 4-Methylhistamine (100 microgram/ml) produced acceleration of the sinus rate from 158 +/- 4 to 173 +/- 5 beats per minute (P less than 0.05) when perfused via the sinus node artery. The effects of the histamine agonists on atrioventricular junctional rhythms were similar to the effects on sinus rhythm. The response of the sinus node to vagal stimulation was attenuated by selective perfusion with histamine; however, the direct negatively chronotropic action of acetylcholine was not affected by histamine. Neither 2-methylhistamine nor 4-methylhistamine affected the response of the sinus node to vagal stimulations. Both 4-methylhistamine and histamine (but not 2-methylhistamine) attenuated (P less than 0.05) the response of the sinus node to stimulation of the right stellate ganglion. The positively chronotropic effects of directly perfused norepinephrine were unaffected by histamine or 4-methylhistamine. These results suggest a neural depressing action of histamine on autonomic efferent fibers. In the atrioventricular junction, both histamine and 2-methylhistamine (but not 4-methylhistamine) had negatively dromotropic effects. Cimetidine (an H2 antagonist) had no significant direct effects on the sinus rate or atrioventricular conduction and failed to prevent the acceleration of the sinus rate produced by local perfusion with 4-methylhistamine.

摘要

在用戊巴比妥钠麻醉的75只犬中,通过选择性灌注窦房结动脉和房室结动脉,研究了2-甲基组胺(H1激动剂)、4-甲基组胺(H2激动剂)和组胺的作用。2-甲基组胺和组胺对窦性心率的影响多变且不一致。当通过窦房结动脉灌注4-甲基组胺(100微克/毫升)时,窦性心率从每分钟158±4次加速至173±5次(P<0.05)。组胺激动剂对房室交界性心律的作用与对窦性心律的作用相似。组胺选择性灌注可减弱窦房结对迷走神经刺激的反应;然而,乙酰胆碱直接的负性变时作用不受组胺影响。2-甲基组胺和4-甲基组胺均不影响窦房结对迷走神经刺激的反应。4-甲基组胺和组胺(但2-甲基组胺不影响)均可减弱(P<0.05)窦房结对右星状神经节刺激的反应。直接灌注去甲肾上腺素的正性变时作用不受组胺或4-甲基组胺影响。这些结果提示组胺对自主神经传出纤维有神经抑制作用。在房室交界区,组胺和2-甲基组胺(但4-甲基组胺不影响)均有负性传导作用。西咪替丁(一种H2拮抗剂)对窦性心率或房室传导无明显直接作用,且不能阻止局部灌注4-甲基组胺所引起的窦性心率加速。

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