Activation of muscle nicotinic acetylcholine receptor channels by nicotinic and muscarinic agonists

被引:46
作者
Akk, G [1 ]
Auerbach, A [1 ]
机构
[1] SUNY Buffalo, Dept Physiol & Biophys, Buffalo, NY 14214 USA
关键词
nicotinic acetylcholine receptor; ion channel; agonist; acetylcholine; nicotine; carbamylcholine; oxotremorine; muscarine;
D O I
10.1038/sj.bjp.0702941
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The dose-response parameters of recombinant mouse adult neuromuscular acetylcholine receptor channels (nAChR) activated by carbamylcholine, nicotine, muscarine and oxotremorine were measured. Rate constants for agonist association and dissociation, and channel opening and closing, were estimated from single-channel kinetic analysis. 2 The dissociation equilibrium constants were (mM): ACh (0.16)<oxotremorine M (0.6)<carbamylcholine (0.8) <nicotine (2.6). 3 The gating equilibrium constants (opening/closing) were: ACh (45)> carbamylcholine (5.1)> oxotremorine M (0.6)>nicotine (0.5)>muscarine (0.15). 4 Rat neuronal alpha(4)beta(2) nAChR can be activated by all of the agonists. However, detailed kinetic analysis was impossible because the recordings lacked clusters representing the activity of a single receptor complex. Thus, the number of channels in the patch was unknown and the activation rate constants could not be determined. 5 Considering both receptor affinity and agonist efficacy, muscarine and oxotremorine are significant agonists of muscle-type nAChR. The results are discussed in terms of structure-function relationships at the nAChR transmitter binding site.
引用
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页码:1467 / 1476
页数:10
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