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加拉明对毒蕈碱受体的抑制作用。

The inhibitory effect of gallamine on muscarinic receptors.

作者信息

Clark A L, Mitchelson F

出版信息

Br J Pharmacol. 1976 Nov;58(3):323-31. doi: 10.1111/j.1476-5381.1976.tb07708.x.

DOI:10.1111/j.1476-5381.1976.tb07708.x
PMID:990587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1667582/
Abstract

1 The inhibitory effect of gallamine (1.1 muM-1.1 mM) on negative inotropic responses to acetylcholine (ACh) or carbachol (CCh) was investigated in isolated electrically stimulated atria of the guinea-pig. Gallamine caused parallel rightward shifts of the dose-response curves to the agonists, with no depression of the maximal response. 2 Gallamine (0.11 - 1.1 mM) produced a greater degree of antagnism towards CCh than towards ACh. With either agonist, the degree of antagonism produced by gallamine in high concentrations was less than that expected for a competitive antagonist.. 3 Similar findings were made when either negative inotropic or chronotropic responses were recorded in spontaneously beating guinea-pig atria. The inhibitory effect of gallamine against the negative inotropic response to cholinomimetics in electrically stimulated atria was not altered either in the presence of propranol (17 muM) or in atria obtained from guinea-pigs pretreated with diisopropylphosphorofluoridate (DEP) 12.5 mumol/kg, in divided doses over 3 days). 4 When ACh was used as the agonist, combination of gallamine with atropine (0.05-0.4 muM) produced dose-ratios which were less than expected for combination of two competitive antagonists. The same phenomenon was observed in atria obtained from guinea-pigs pretreated with DFP. 5 It is suggested that the antagonism produced by gallamine is a type of non-competitive inhibition, which has been termed "metaffinoid antagonism". An antagonist of this type allosterically alters the affinity of the agonist for its binding site, rather than changing the effectiveness of the agonist-receptor interaction.

摘要

1 在豚鼠离体电刺激心房中,研究了加拉明(1.1 μM - 1.1 mM)对乙酰胆碱(ACh)或卡巴胆碱(CCh)负性肌力反应的抑制作用。加拉明使激动剂的剂量 - 反应曲线平行右移,最大反应无降低。2 加拉明(0.11 - 1.1 mM)对CCh产生的拮抗程度大于对ACh的拮抗程度。对于任何一种激动剂,高浓度加拉明产生的拮抗程度均小于竞争性拮抗剂预期的程度。3 在自发搏动的豚鼠心房中记录负性肌力或变时反应时,也得到了类似的结果。在普萘洛尔(17 μM)存在的情况下,或在经二异丙基氟磷酸酯(DEP)12.5 μmol/kg预处理(分3天给药)的豚鼠心房中,加拉明对电刺激心房中拟胆碱药负性肌力反应的抑制作用均未改变。4 当使用ACh作为激动剂时,加拉明与阿托品(

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本文引用的文献

1
The pharmacology of Flaxedil, with observations on certain analogs.加拉碘铵的药理学及某些类似物的观察
Ann N Y Acad Sci. 1951 Oct;54(3):373-94. doi: 10.1111/j.1749-6632.1951.tb39932.x.
2
An assessment of flaxedil (Gallamine triethiodide, B.P.).三碘季铵酚(英国药典)的评估。
Proc R Soc Med. 1951 May;44(5):375-88. doi: 10.1177/003591575104400509.
3
THE UPTAKE OF ATROPINE AND RELATED DRUGS BY INTESTINAL SMOOTH MUSCLE OF THE GUINEA-PIG IN RELATION TO ACETYLCHOLINE RECEPTORS.豚鼠肠道平滑肌对阿托品及相关药物的摄取与乙酰胆碱受体的关系
Proc R Soc Lond B Biol Sci. 1965 Aug 24;163:1-44. doi: 10.1098/rspb.1965.0058.
4
THE INFLUENCE OF THE INTERVAL BETWEEN BEATS ON MYOCARDIAL CONTRACTILITY.心动周期对心肌收缩力的影响。
Pharmacol Rev. 1963 Sep;15:601-52.
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.
6
A theoretical basis of molecular pharmacology; II. Interactions of one or two compounds with two interdependent receptor systems.分子药理学的理论基础;II. 一种或两种化合物与两个相互依赖的受体系统的相互作用
Arzneimittelforschung. 1956 Oct;6(10):611-21.
7
The effect on the isolated rabbit heart of vagal stimulation and its modification by cocaine, hexamethonium and ouabain.迷走神经刺激对离体兔心脏的影响以及可卡因、六甲铵和哇巴因对其的影响。
J Physiol. 1956 Mar 28;131(3):678-89. doi: 10.1113/jphysiol.1956.sp005493.
8
The inhibition of cholinesterases by antagonists of acetylcholine and histamine.乙酰胆碱和组胺拮抗剂对胆碱酯酶的抑制作用。
Br J Pharmacol Chemother. 1954 Mar;9(1):76-83. doi: 10.1111/j.1476-5381.1954.tb00820.x.
9
Responses of acetylcholinesterase from Torpedo marmorata to salts and curarizing drugs.电鳐乙酰胆碱酯酶对盐类和箭毒化药物的反应。
Mol Pharmacol. 1966 Sep;2(5):369-92.
10
The nicotinic effects of choline esters and of nicotine in guinea pig atria.胆碱酯类和尼古丁对豚鼠心房的烟碱样作用。
J Pharmacol Exp Ther. 1966 Apr;152(1):29-36.