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抗胆碱酯酶药物对离子电泳诱发的终板电流的影响。

The effect of anticholinesterase drugs on the ionophoretically-evoked end-plate currents.

作者信息

Scuka M

机构信息

Department of Biology, University of Trieste, Italy.

出版信息

Pflugers Arch. 1987 Nov;410(4-5):428-32. doi: 10.1007/BF00586521.

DOI:10.1007/BF00586521
PMID:3501570
Abstract

In order to study the sensitivity of acetylcholine (ACh) receptors exposed to anticholinesterase drugs, the ionophoretically evoked end-plate currents (e.p.c.i) in frog sartorius muscle were studied. During treatment with prostigmine (PST, 3 microM) or methanesulfonyl fluoride (MSF, 1-2 mM), the amplitude of the e.p.c.i evoked by ACh was first increased, reaching its maximum (200-400%) after 20-30 min and then decreased. If these experiments were repeated by applying carbachol (CCh) instead of ACh, an increase, although less pronounced (30-100%), was also observed. The results obtained by applying CCh cannot be ascribed to the inhibition of ACh-esterase, as CCh is not hydrolysed by this enzyme. Therefore, a direct action of both drugs on the ACh-receptor channel complex is suggested. From the comparison of the effects of PST and MSF on the responses to CCh and ACh applications, it is calculated that 20-25% of the increased response to ACh during PST treatment can be ascribed to the direct effect on the ACh-receptor channel complex. During MSF treatment, this amount results in 13-15%. The changes of the time course of the e.p.c.i (evoked by CCh or ACh), which is prolonged in the presence of PST and shortened during the maximum effect of MSF, suggest that the direct action of both studied drugs is different.

摘要

为了研究暴露于抗胆碱酯酶药物下的乙酰胆碱(ACh)受体的敏感性,对蛙缝匠肌中离子电泳诱发的终板电流(e.p.c.i)进行了研究。在用新斯的明(PST,3 microM)或甲磺酰氟(MSF,1 - 2 mM)处理期间,ACh诱发的e.p.c.i的幅度首先增加,在20 - 30分钟后达到最大值(200 - 400%),然后下降。如果用卡巴胆碱(CCh)代替ACh重复这些实验,也观察到了增加,尽管不太明显(30 - 100%)。应用CCh所获得的结果不能归因于对ACh酯酶的抑制,因为CCh不会被这种酶水解。因此,提示这两种药物对ACh受体通道复合物有直接作用。通过比较PST和MSF对CCh和ACh应用反应的影响计算得出,在PST处理期间对ACh增加的反应中,20 - 25%可归因于对ACh受体通道复合物的直接作用。在MSF处理期间,这个比例为13 - 15%。e.p.c.i(由CCh或ACh诱发)的时间进程变化,在PST存在时延长,在MSF的最大作用期间缩短,表明所研究的两种药物的直接作用是不同的。

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引用本文的文献

1
Effects of irreversible and reversible cholinesterase inhibitors on single acetylcholine-activated channels.不可逆和可逆性胆碱酯酶抑制剂对单个乙酰胆碱激活通道的影响。
J Membr Biol. 1992 Jan;125(1):41-8. doi: 10.1007/BF00235796.

本文引用的文献

1
Actions of anti-cholinesterases on endplate potential of frog muscle.抗胆碱酯酶对蛙肌终板电位的作用。
J Neurophysiol. 1949 Jan;12(1):59-80. doi: 10.1152/jn.1949.12.1.59.
2
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.
3
The nature of the interactions of pyridostigmine with the nicotinic acetylcholine receptor-ionic channel complex. I. Agonist, desensitizing, and binding properties.吡啶斯的明与烟碱型乙酰胆碱受体-离子通道复合物的相互作用性质。I. 激动剂、脱敏和结合特性。
Mol Pharmacol. 1984 Jan;25(1):92-101.
4
The nature of the interactions of pyridostigmine with the nicotinic acetylcholine receptor-ionic channel complex. II. Patch clamp studies.吡啶斯的明与烟碱型乙酰胆碱受体 - 离子通道复合物的相互作用性质。II. 膜片钳研究。
Mol Pharmacol. 1984 Jan;25(1):102-12.
5
Physostigmine prolongs the elementary event underlying decay of inhibitory postsynaptic currents in Aplysia.毒扁豆碱延长了海兔抑制性突触后电流衰减的基本事件。
J Neurosci. 1983 Dec;3(12):2607-13. doi: 10.1523/JNEUROSCI.03-12-02607.1983.
6
Possible role of acetylcholinesterase in regulation of postsynaptic receptor efficacy at a central inhibitory synapse of Aplysia.乙酰胆碱酯酶在调节海兔中枢抑制性突触处突触后受体效能中的可能作用。
Nature. 1983 Feb 24;301(5902):710-2. doi: 10.1038/301710a0.
7
The molecular forms of cholinesterase and acetylcholinesterase in vertebrates.脊椎动物体内胆碱酯酶和乙酰胆碱酯酶的分子形式。
Annu Rev Neurosci. 1982;5:57-106. doi: 10.1146/annurev.ne.05.030182.000421.
8
Intracellular calcium and desensitization of acetylcholine receptors.细胞内钙与乙酰胆碱受体的脱敏作用
Proc R Soc Lond B Biol Sci. 1980 Sep 26;209(1176):447-52. doi: 10.1098/rspb.1980.0106.
9
A study of the end-plate potential in sodium deficient solution.低钠溶液中终板电位的研究。
J Physiol. 1968 Sep;198(1):81-90. doi: 10.1113/jphysiol.1968.sp008594.
10
Effect of prostigmine on the time course of the end-plate potential in the rat diaphragm.新斯的明对大鼠膈肌终板电位时间进程的影响。
J Physiol. 1971 Mar;213(3):533-44. doi: 10.1113/jphysiol.1971.sp009398.