POTENTIATION OF ACETYLCHOLINE RESPONSES IN XENOPUS EMBRYONIC MUSCLE-CELLS BY DIBUTYRYL-CAMP

被引:13
作者
FU, WM
机构
[1] Department of Pharmacology, College of Medicine, National Taiwan University, Taipei
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1993年 / 425卷 / 5-6期
关键词
NICOTINIC RECEPTOR; ACETYLCHOLINE CHANNEL; EMBRYONIC MUSCLE CELLS; PROTEIN KINASE A; XENOPUS; BT(2)CAMP; DEVELOPMENTAL CHANGE; DESENSITIZATION;
D O I
10.1007/BF00374870
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Application of membrane-permeable analogues of adenosine 3',5'-(cyclic)monophosphate (cAMP) or forskolin to embryonic muscle cells of 1-day-old Xenopus cultures altered the response of the myocyte to iontophoretically applied acetylcholine (ACh). The initial amplitude and the decay time of the ACh-induced currents were elevated, and the rate of ACh-induced channel desensitization was increased. Single-channel recordings showed that cAMP analogues increased the mean open time of the low-conductance ACh channels, without affecting the single-channel conductance. Interestingly this effect on ACh channels disappeared in myocytes of 3-day-old cultures, suggesting developmental changes in the susceptibility of the ACh channel to modulation. A possible involvement of cAMP in modulating the synaptic activity of early developing synapses was further indicated by prolonged decay times of spontaneous synaptic currents following treatment with dibutyryl-cAMP (Bt(2)cAMP). Factors released from the nerve terminals, if they activate the muscle adenylate cyclase system, could thus enhance the synaptic response during synaptogenesis.
引用
收藏
页码:439 / 445
页数:7
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