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[亲和力对铵化合物作用于骨骼肌胆碱能受体的作用类型的影响]

[The effect of affinity on the type of action of ammonium compounds on skeletal muscle cholinoreceptors].

作者信息

Danilov A F, Lavrent'eva V V

出版信息

Eksp Klin Farmakol. 1996 Nov-Dec;59(6):10-2.

PMID:9181862
Abstract

The dependence of the mode of action (agonist or antagonist) of ammonium compounds on the acetylcholine receptors (AcR) of frog skeletal muscles on their affinity for AcR was studied in experiments on musculus rectus abdominis of Rana temporaria frogs. The mode of action of the compounds proved to be dependent on the degree of the affinity and on the character of their intermolecular interactions with the receptors. The affinity of compounds of the polymethylene-bis-trimethylammonium series is determined by electrostatic and hydrophobic interaction with the AcR. In this case compounds with a low affinity constant (Ka) are poor antagonists, compounds with high Ka are strong antagonists, and compounds with intermediate Ka are partly agonists. Compounds whose affinity is determined not only by the electrostatic and hydrophobic but also by the dipole-dipole interaction (series D compounds) are pure and strong agonists.

摘要

在对泽蛙腹直肌进行的实验中,研究了铵化合物对青蛙骨骼肌乙酰胆碱受体(AcR)的作用方式(激动剂或拮抗剂)对其与AcR亲和力的依赖性。结果证明,这些化合物的作用方式取决于亲和力的程度及其与受体分子间相互作用的性质。聚亚甲基 - 双 - 三甲基铵系列化合物的亲和力由与AcR的静电和疏水相互作用决定。在这种情况下,亲和力常数(Ka)低的化合物是弱拮抗剂,Ka高的化合物是强拮抗剂,Ka中等的化合物是部分激动剂。其亲和力不仅由静电和疏水作用,还由偶极 - 偶极相互作用决定的化合物(D系列化合物)是纯的强激动剂。

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