首页> 美国卫生研究院文献>The Journal of Physiology >The nature of the receptor mediating stimulant effects of histamine on rapidly adapting vagal afferents in the lungs.
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The nature of the receptor mediating stimulant effects of histamine on rapidly adapting vagal afferents in the lungs.

机译:组胺对肺中快速适应性迷走神经传入的受体介导刺激作用的性质。

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摘要

1. The effects of histamine H1- and H2-agonists on these airway sensory receptors were also examined. 2. Neither I.V. infusion of metiamide (5 mg/kg, min for 35 min) in seven experiments, nor I.V. bolus injection of burimamide (15 mg/kg) in six other experiments, both substances being H2-antagonists, altered the response of rapidly adapting receptors to aerosols of histamine (from 0.1 or 1.0% solutions). 3. Chlorpheniramine (H1-antagonist), 2--5 mg/kg, I.V., completely abolished responses of rapidly adapting receptors to histamine in seven experiments in which metiamide had been given previously and in seven other preparations in which it had not, but had no effect on responses to prostaglandin F2 alpha. Chlorpheniramine itself caused a brief stimulation of rapidly adapting receptors. 4. The H2-agonist S-[3-(N,N-dimethylamino) propyl] isothiourea (Dimaprit), given as aerosol (1% solution for 2 min) or I.V. (2 mg/kg), was without effect on activity of four airway rapidly adapting receptors. These receptors were stimulated, however, by the H1-agonist 2,(2 pyridylethylamine) dihydrochloride (PEA), administered both as aerosol (from a 10% solution) and I.V. (0.4--2 mg/kg). These stimulant effects were abolished by chlorpheniramine. 5. The results indicate that stimulation of airway rapidly adapting receptors by histamine is mediated by histamine H1-receptors.
机译:1.还检查了组胺H1-和H2-激动剂对这些气道感觉受体的作用。 2.双方在七个实验中输注了甲酰胺(5 mg / kg,分钟持续35分钟),也没有静脉注射。在其他六个实验中,大剂量推注burimamide(15 mg / kg),两种物质均为H2拮抗剂,改变了快速适应性受体对组胺气雾剂的反应(0.1或1.0%溶液)。 3.在先前已给予甲酰胺的7项实验和未给予甲胺的7项制剂中,氯苯那敏(H1拮抗剂)2--5 mg / kg静脉注射完全消除了快速适应受体对组胺的反应。对前列腺素F2α的反应没有影响。氯苯那敏本身会短暂刺激快速适应性受体。 4.H 2-激动剂S- [3-(N,N-二甲基氨基)丙基]异硫脲(Dimaprit),以气雾剂(1%溶液,持续2分钟)或静脉注射。 (2 mg / kg)对四种气道快速适应受体的活性没有影响。然而,这些受体被H1-激动剂2,(2-吡啶基乙胺)二盐酸盐(PEA)刺激,以气雾剂(从10%溶液中)和静脉内给药。 (0.4--2 mg / kg)。氯苯那敏消除了这些刺激作用。 5.结果表明,组胺H1受体介导组胺刺激气道快速适应性受体。

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