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犬气管肌肉组织和血管系统中组胺受体的药理学分析(原位)

Pharmacological analysis of histamine receptors in musculature and vasculature of the dog trachea in situ.

作者信息

Himori N, Taira N

出版信息

Br J Pharmacol. 1978 Dec;64(4):553-8. doi: 10.1111/j.1476-5381.1978.tb17317.x.

Abstract

1 The role of histamine H1- and H2-receptors in the musculature and vasculature of the dog trachea was investigated in the blood-perfused trachea in situ. 2 Histamine and acetylcholine caused increases in blood flow (tracheal, vasodilatation) and in intraluminal pressure (tracheal constriction) in a dose-dependent manner. Histamine was almost equipotent to acetylcholine in causing tracheal vasodilatation but was about 30 times less potent in causing tracheal constriction. 3 The histamine H2-receptor agonist, dimaprit, caused a dose-dependent increase in tracheal blood flow but failed to cause tracheal constriction. 4 The tracheal constriction produced by histamine was inhibited strongly by diphenhydramine but not modifed by metiamide. The tracheal vasodilatation produced by histamine was antagonized by both diphenhydramine and metiamide; diphenhydramine was more effective than metiamide. 5 It is concluded that in the tracheal musculature, histamine receptors are exclusively of the H1-type and mediate constriction, whereas in the tracheal vasculature, both histamine H1- and H2-receptors mediate vasodilatation but histamine H1-receptors are predominant.

摘要
  1. 研究了组胺H1和H2受体在犬气管肌肉组织和血管系统中的作用,实验采用原位血液灌注的气管。2. 组胺和乙酰胆碱以剂量依赖的方式引起血流量增加(气管血管舒张)和管腔内压力升高(气管收缩)。组胺在引起气管血管舒张方面几乎与乙酰胆碱等效,但在引起气管收缩方面的效力约低30倍。3. 组胺H2受体激动剂二甲双胍引起气管血流量剂量依赖性增加,但未引起气管收缩。4. 组胺引起的气管收缩受到苯海拉明的强烈抑制,但不受甲硫米特的影响。组胺引起的气管血管舒张受到苯海拉明和甲硫米特的拮抗;苯海拉明比甲硫米特更有效。5. 得出的结论是,在气管肌肉组织中,组胺受体完全是H1型,介导收缩,而在气管血管系统中,组胺H1和H2受体均介导血管舒张,但组胺H1受体占主导地位。

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本文引用的文献

1
The physiological action of beta-iminazolylethylamine.β-咪唑基乙胺的生理作用。
J Physiol. 1910 Dec 31;41(5):318-44. doi: 10.1113/jphysiol.1910.sp001406.
5
Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.

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