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海美胆碱-3通过作用于海兔中枢突触处的突触前烟碱受体来促进乙酰胆碱的释放。

Hemicholinium-3 facilitates the release of acetylcholine by acting on presynaptic nicotinic receptors at a central synapse in Aplysia.

作者信息

Poulain B, Fossier P, Baux G, Tauc L

机构信息

Laboratoire de Neurobiologie Cellulaire et Moléculaire, C.N.R.S., Gif sur Yvette, France.

出版信息

Brain Res. 1987 Dec 1;435(1-2):63-70. doi: 10.1016/0006-8993(87)91587-3.

Abstract

The effects of hemicholinium-3 (HC-3) on acetylcholine (ACh) release were studied on central inhibitory or excitatory synapses of Aplysia californica. HC-3 was used at concentrations below 10(-5) M, which did not affect choline uptake by this preparation. Statistical analysis of the synaptic noise evoked by sustained depolarization of the presynaptic neuron allowed us to calculate the amplitude and mean duration of the miniature postsynaptic responses at an inhibitory synapse in the buccal ganglion. Taking into account the modifications of miniature and evoked responses, it was concluded that HC-3 potentiates ACh release. A similar presynaptic effect was observed at an excitatory synapse in the abdominal ganglion. This facilitation of ACh release was prevented by tubocurarine or hexamethonium, pointing to an agonistic action of HC-3 on nicotinic presynaptic receptors implicated in a positive feedback on ACh release. The possible blockage of muscarinic presynaptic receptors by HC-3 was also considered. Hemicholinium-15 was without effect on ACh release but was nevertheless able to prevent the presynaptic action of HC-3.

摘要

研究了半胱氨酸-3(HC-3)对加州海兔中枢抑制性或兴奋性突触中乙酰胆碱(ACh)释放的影响。使用浓度低于10^(-5) M的HC-3,该浓度不会影响此制剂对胆碱的摄取。对突触前神经元持续去极化诱发的突触噪声进行统计分析,使我们能够计算出颊神经节中抑制性突触处微小突触后反应的幅度和平均持续时间。考虑到微小反应和诱发反应的变化,得出HC-3增强ACh释放的结论。在腹神经节的兴奋性突触处也观察到类似的突触前效应。筒箭毒碱或六甲铵可阻止这种ACh释放的促进作用,表明HC-3对参与ACh释放正反馈的烟碱型突触前受体具有激动作用。还考虑了HC-3可能对毒蕈碱型突触前受体的阻断作用。半胱氨酸-15对ACh释放无影响,但仍能够阻止HC-3的突触前作用。

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