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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.

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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