Bukharaeva E A, Nikol'skiĭ E E, Giniatullin R A
Neirofiziologiia. 1986;18(5):586-93.
The action of cholinergic drugs on spontaneous quantal transmitter release has been investigated in the frog sartorius muscle. Acetylcholine and carbacholine decreased the miniature end-plate potential frequency. These presynaptic effects had no dependence on the potassium concentration in the bath solution. Nicotinic agonists--nicotine, tetramethylammonium and suberyldicholine had a similar effect, while muscarinic agents--methylfurmetide, oxotremorine and F-2268 (L- and D-stereoisomers) did not affect the transmitter release. The presynaptic effects of carbacholine and acetylcholine were abolished neither by atropine nor by d-tubocurarine and bensohexonium. It is suggested that there are nicotinic receptors on the frog motor nerve terminals that modify spontaneous quantal transmitter release and differ pharmacologically from nicotinic end-plate, ganglionic and presynaptic receptors of higher vertebrates.
已在蛙缝匠肌中研究了胆碱能药物对自发量子递质释放的作用。乙酰胆碱和卡巴胆碱降低了微小终板电位频率。这些突触前效应不依赖于浴液中的钾浓度。烟碱样激动剂——尼古丁、四甲铵和辛二酰胆碱有类似作用,而毒蕈碱样药物——甲呋硫胺、氧化震颤素和F-2268(L-和D-立体异构体)不影响递质释放。卡巴胆碱和乙酰胆碱的突触前效应既不被阿托品阻断,也不被d-筒箭毒碱和苯磺铵阻断。提示蛙运动神经末梢存在烟碱样受体,其可调节自发量子递质释放,且在药理学上不同于高等脊椎动物的烟碱样终板、神经节和突触前受体。