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硝酸甘油使交感神经末梢释放去甲肾上腺素,从而引起心房出现正性变时和变力反应。

Positive chronotropic and inotropic responses to release of norepinephrine from sympathetic nerve terminals produced by nitroglycerin in atria.

作者信息

Ma S X, Long J P

机构信息

Department of Pharmacology, College of Medicine, University of Iowa, Iowa City 52242.

出版信息

Arch Int Pharmacodyn Ther. 1991 Jan-Feb;309:125-36.

PMID:1909520
Abstract

Nitroglycerin produced concentration-dependent increases in spontaneous rate and enhancements of positive chronotropic and inotropic responses to transmural stimulation of isolated right guinea-pig atria. The effects of nitroglycerin were significantly potentiated by desmethylimipramine, which is an inhibitor of norepinephrine uptake, and were significantly inhibited by either guanethidine, which inhibits release of norepinephrine, or alpha-methyl-p-tyrosine, which inhibits synthesis of norepinephrine. The effects of nitroglycerin were not modified by either prazosin or atropine, but were significantly inhibited by either the beta-adrenoceptor antagonist propranolol or the alpha 2-adrenoceptor antagonist yohimbine. Nitroglycerin significantly increased the concentration of norepinephrine in the medium bathing atria and the 3,4-dihydroxyphenylglycol concentration in the atrial tissue, which were quantified using high-performance liquid chromatography with electrochemical detection. The atrial responses to nitroglycerin appear to mimic sympathetic neuronal activities and may involve the modulatory role of alpha 2-adrenoceptors in the release of norepinephrine.

摘要

硝酸甘油可使豚鼠离体右心房的自发频率呈浓度依赖性增加,并增强对跨壁刺激的正性变时和变力反应。去甲丙咪嗪(一种去甲肾上腺素摄取抑制剂)可显著增强硝酸甘油的作用,而胍乙啶(抑制去甲肾上腺素释放)或α-甲基对酪氨酸(抑制去甲肾上腺素合成)则可显著抑制其作用。硝酸甘油的作用不受哌唑嗪或阿托品的影响,但可被β-肾上腺素能受体拮抗剂普萘洛尔或α2-肾上腺素能受体拮抗剂育亨宾显著抑制。硝酸甘油可显著增加心房灌流液中去甲肾上腺素的浓度以及心房组织中3,4-二羟基苯乙二醇的浓度,这些浓度通过高效液相色谱-电化学检测法定量。心房对硝酸甘油的反应似乎模拟了交感神经神经元的活动,可能涉及α2-肾上腺素能受体在去甲肾上腺素释放中的调节作用。

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