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本文引用的文献

1
Receptors in the trachea and bronchi of the cat.猫气管和支气管中的受体。
J Physiol. 1954 Jan;123(1):71-104. doi: 10.1113/jphysiol.1954.sp005034.
2
Definition and antagonism of histamine H 2 -receptors.组胺H2受体的定义与拮抗作用。
Nature. 1972 Apr 21;236(5347):385-90. doi: 10.1038/236385a0.
3
Metiamide--an orally active histamine H2-receptor antagonist.甲硫米特——一种口服有效的组胺H2受体拮抗剂。
Agents Actions. 1973 Oct;3(3):133-7. doi: 10.1007/BF01965723.
4
Properties of 'irritant' receptors in canine lung.犬肺中“刺激性”受体的特性
Respir Physiol. 1975 Oct;25(1):9-22. doi: 10.1016/0034-5687(75)90047-x.
5
Stimulation of 'irritant' receptors and afferent C-fibres in the lungs by prostaglandins.前列腺素对肺部“刺激性”受体和传入C纤维的刺激作用。
Nature. 1976 Dec 2;264(5585):451-3. doi: 10.1038/264451a0.
6
Mechanisms by which histamine stimulates rapidly adapting receptors in dog lungs.组胺刺激犬肺快速适应性受体的机制。
J Appl Physiol Respir Environ Exerc Physiol. 1977 Sep;43(3):397-402. doi: 10.1152/jappl.1977.43.3.397.
7
Dimaprit -(S-[3-(N,N-dimethylamino)prophyl]isothiourea) - a highly specific histamine H2 -receptor agonist. Part 1. Pharmacology.二甲双胍 -(S-[3-(N,N-二甲基氨基)丙基]异硫脲)- 一种高度特异性的组胺H2受体激动剂。第一部分。药理学。
Agents Actions. 1977 Mar;7(1):31-7. doi: 10.1007/BF01964878.
8
Histamine H1- and H2-receptors in pulmonary and systemic vasculature of the dog.犬肺血管和体循环血管中的组胺H1和H2受体。
Am J Physiol. 1975 Oct;229(4):1008-13. doi: 10.1152/ajplegacy.1975.229.4.1008.
9
Chemical differentiation of histamine H1- and H2-receptor agonists.组胺H1和H2受体激动剂的化学鉴别
J Med Chem. 1975 Sep;18(9):905-9. doi: 10.1021/jm00243a009.
10
Histamine (second of two parts).组胺(两部分中的第二部分)。
N Engl J Med. 1976 Feb 5;294(6):320-5. doi: 10.1056/NEJM197602052940608.

介导组胺对肺内快速适应迷走传入神经刺激作用的受体的性质。

The nature of the receptor mediating stimulant effects of histamine on rapidly adapting vagal afferents in the lungs.

作者信息

Sampson S R, Vidruk E H

出版信息

J Physiol. 1979 Feb;287:509-18. doi: 10.1113/jphysiol.1979.sp012673.

DOI:10.1113/jphysiol.1979.sp012673
PMID:430433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1281509/
Abstract
  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.
摘要
  1. 还研究了组胺H1和H2激动剂对这些气道感觉受体的作用。2. 在七项实验中,静脉输注甲硫米特(5毫克/千克,持续35分钟),以及在另外六项实验中静脉推注布立马胺(15毫克/千克),这两种物质均为H2拮抗剂,均未改变快速适应性受体对组胺气雾剂(来自0.1%或1.0%溶液)的反应。3. 氯苯那敏(H1拮抗剂),静脉注射2 - 5毫克/千克,在七项先前给予甲硫米特的实验以及另外七项未给予甲硫米特的制剂实验中,完全消除了快速适应性受体对组胺的反应,但对前列腺素F2α的反应没有影响。氯苯那敏本身引起快速适应性受体的短暂刺激。4. H2激动剂S-[3-(N,N-二甲基氨基)丙基]异硫脲(地马普明),以气雾剂(1%溶液,持续2分钟)或静脉注射(2毫克/千克)给药,对四个气道快速适应性受体的活性没有影响。然而,这些受体受到H1激动剂2,(2-吡啶基乙胺)二盐酸盐(PEA)的刺激,PEA以气雾剂(来自10%溶液)和静脉注射(0.4 - 2毫克/千克)给药。这些刺激作用被氯苯那敏消除。5. 结果表明,组胺对气道快速适应性受体的刺激是由组胺H1受体介导的。