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毒蕈碱和阿托品的作用表明,青蛙运动神经末梢存在抑制性自身受体,但在神经传递过程中未被激活。

The effects of muscarine and atropine reveal that inhibitory autoreceptors are present on frog motor nerve terminals but are not activated during transmission.

作者信息

Arenson M S

机构信息

Department of Pharmacology, St. Bartholomew's Hospital Medical College, University of London, UK.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1991 Feb;343(2):128-33. doi: 10.1007/BF00168599.

Abstract

The role of presynaptic muscarinic receptors in modulating neuromuscular transmission was studied in the isolated sartorius muscle of the frog using electrophysiological techniques. In low calcium solutions muscarine reduced mEPP frequency and the quantal of EPPs. In solutions containing the normal calcium concentration the effect of muscarine on quantal content, but not the effect on mEPP frequency, was somewhat attenuated. Muscarine-induced reductions in the parameters of ACh release were prevented by atropine. Irrespective of the calcium concentration, atropine had no effect on mEPP frequency except where fibres were pretreated with glycerol. In experiments where evoked acetylcholine release was maintained at physiologically relevant levels, atropine had no effect on the quantal content of EPPs evoked at low frequency or on the extent of rundown in trains of EPPs evoked at high frequency.

摘要

利用电生理技术,在青蛙离体缝匠肌中研究了突触前毒蕈碱受体在调节神经肌肉传递中的作用。在低钙溶液中,毒蕈碱降低微小终板电位(mEPP)频率和终板电位(EPP)的量子含量。在含有正常钙浓度的溶液中,毒蕈碱对量子含量的影响有所减弱,但对mEPP频率的影响未减弱。毒蕈碱引起的乙酰胆碱(ACh)释放参数降低可被阿托品阻止。无论钙浓度如何,阿托品对mEPP频率均无影响,但在用甘油预处理纤维的情况下除外。在将诱发的乙酰胆碱释放维持在生理相关水平的实验中,阿托品对低频诱发的EPP的量子含量或高频诱发的EPP串中的衰减程度均无影响。

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