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阿托品对青蛙神经肌肉接头作用的分析。

Analysis of atropine action at the frog neutromuscular junction.

作者信息

Feltz A, Large W A, Trautmann A

出版信息

J Physiol. 1977 Jul;269(1):109-30. doi: 10.1113/jphysiol.1977.sp011895.

DOI:10.1113/jphysiol.1977.sp011895
PMID:302330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1283705/
Abstract
  1. Atropine action on the end-plate currents (e.p.c.s) has been analysed at the macroscopic and elementary levels. 2. The shortening effect of atropine on the e.p.c. and m.e.p.c. level can be fully explained by a reduction of the life time of the elementary current: this effect is markedly increased at more hyperpolarized membrane potentials and at higher concentrations of atropine. 3. It is therefore suggested that atropine binds to the open acetylcholine-receptor complex, leading to a state with a null conductance. According to this model, the forward rate constant of atropine binding could be calculated and was of the order of 10(7) M-1 S-1 AT -90 MV and 20-22 degrees C. 4. Although the conductance at the peak of the e.p.c. is reduced by atropine and becomes voltage sensitive, the elementary conductance is affected neither by voltage nor by atropine. 5. The exclusive binding of atropine to the activated ACh-receptor complex, as proposed above, does not appear to explain this phenomenon. Another binding occurring before the channel is open with a dissociation constant of 60 micrometer could account for this effect.
摘要
  1. 已在宏观和基本水平上分析了阿托品对终板电流(e.p.c.s)的作用。2. 阿托品对e.p.c.和微小终板电流(m.e.p.c.)水平的缩短作用可以通过基本电流寿命的缩短来充分解释:在更超极化的膜电位和更高浓度的阿托品作用下,这种作用会明显增强。3. 因此有人提出,阿托品与开放的乙酰胆碱受体复合物结合,导致一种零电导状态。根据该模型,可以计算出阿托品结合的正向速率常数,在-90 mV和20 - 22℃时约为10(7) M-1 S-1。4. 尽管阿托品会降低e.p.c.峰值处的电导并使其变得对电压敏感,但基本电导既不受电压影响也不受阿托品影响。5. 如上文所提出的,阿托品与活化的乙酰胆碱受体复合物的排他性结合似乎无法解释这一现象。在通道开放之前发生的另一种结合,其解离常数为60微米,可能解释这种效应。

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本文引用的文献

1
Active phase of frog's end-plate potential.青蛙终板电位的活动期
J Neurophysiol. 1959 Jul;22(4):395-411. doi: 10.1152/jn.1959.22.4.395.
2
A study of the desensitization produced by acetylcholine at the motor end-plate.一项关于乙酰胆碱在运动终板产生脱敏作用的研究。
J Physiol. 1957 Aug 29;138(1):63-80. doi: 10.1113/jphysiol.1957.sp005838.
3
The action of tubocurarine and atropine on the normal and denervated rat diaphragm.筒箭毒碱和阿托品对正常及去神经大鼠膈肌的作用。
J Physiol. 1967 Jan;188(1):53-66. doi: 10.1113/jphysiol.1967.sp008123.
4
Different action of atropine and some analogues on the end-plate potentials and induced acetylcholine potentials.阿托品及一些类似物对终板电位和诱发乙酰胆碱电位的不同作用。
Experientia. 1969 Jun 15;25(6):618-9. doi: 10.1007/BF01896548.
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The effect of atropine on the frog sartorius neuromuscular junction.阿托品对青蛙缝匠肌神经肌肉接头的作用。
J Physiol. 1968 Mar;195(2):493-503. doi: 10.1113/jphysiol.1968.sp008470.
6
The statistical nature of the acetycholine potential and its molecular components.乙酰胆碱电位及其分子成分的统计学性质。
J Physiol. 1972 Aug;224(3):665-99. doi: 10.1113/jphysiol.1972.sp009918.
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A quantitative description of end-plate currents.终板电流的定量描述。
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8
An electrophysiological study of the effects of D-tubocurarine, atropine, and alpha-bungarotoxin on the cholinergic receptor in innervated and chronically denervated mammalian skeletal muscles.关于筒箭毒碱、阿托品和α-银环蛇毒素对去神经和长期失神经支配的哺乳动物骨骼肌中胆碱能受体作用的电生理研究。
Exp Neurol. 1974 May;43(2):375-98. doi: 10.1016/0014-4886(74)90179-4.
9
The effect of alpha-bungarotoxin on acetylcholine receptors.α-银环蛇毒素对乙酰胆碱受体的作用。
Br J Pharmacol. 1973 Sep;49(1):138-9. doi: 10.1111/j.1476-5381.1973.tb08278.x.
10
Effect of histrionicotoxin on the ionic conductance modulator of the cholinergic receptor: a quantitative analysis of the end-plate current.组胺毒素对胆碱能受体离子电导调节剂的作用:终板电流的定量分析
J Pharmacol Exp Ther. 1974 May;189(2):513-24.