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拟胆碱药可诱导θ节律并降低海马锥体细胞兴奋性。

Cholinomimetics induce theta rhythm and reduce hippocampal pyramidal cell excitability.

作者信息

Olpe H R, Klebs K, Küng E, Campiche P, Glatt A, Ortmann R, D'Amato F, Pozza M F, Mondadori C

机构信息

Biology Research Laboratories, Ciba-Geigy Ltd., Basel, Switzerland.

出版信息

Eur J Pharmacol. 1987 Oct 13;142(2):275-83. doi: 10.1016/0014-2999(87)90117-8.

Abstract

The actions of cholinomimetics and of physostigmine were tested on two parameters reflecting hippocampal activity, namely theta activity and pyramidal cell excitability. In rats pretreated with methylscopolamine and anaesthetized with urethane i.v. administration of the cholinomimetics oxotremorine and arecoline and the cholinesterase blocker physostigmine evoked theta wave activity in the hippocampus, which was blocked by scopolamine. Spectral analysis demonstrated that the frequency of the theta waves induced was dose-related, ranging from about 3 Hz to between 5 and 6 Hz. theta Activity could not be induced by arecoline in animals with large septal lesions. Pyramidal cell excitability is known to be increased by endogenous acetylcholine released from cholinergic fibres. In the present study, however, i.v. injections of oxotremorine, arecoline and physostigmine in doses that induce theta activity diminished the excitability of CA1 pyramidal cells in a dose-dependent manner, as judged by the reduction in the amplitude of the population spike and the dendritic epsp. These depressant effects were attenuated by scopolamine but not by methylscopolamine. The depressant effect of arecoline was attenuated in rats with extensive lesions in the medial septal area. The present findings demonstrate that exogenously administered cholinomimetics only partly mimic the action of endogenous acetylcholine in the hippocampus. The central sites of action of exogenously administered cholinomimetics for mediation of theta activity and alteration of pyramidal cell excitability remain to be elucidated.

摘要

在反映海马体活动的两个参数上,即θ波活动和锥体细胞兴奋性,对拟胆碱药和毒扁豆碱的作用进行了测试。在用甲基东莨菪碱预处理并经静脉注射乌拉坦麻醉的大鼠中,静脉注射拟胆碱药氧化震颤素和槟榔碱以及胆碱酯酶阻滞剂毒扁豆碱可诱发海马体中的θ波活动,而这种活动可被东莨菪碱阻断。频谱分析表明,所诱发的θ波频率与剂量相关,范围从约3赫兹到5至6赫兹之间。在有大面积中隔损伤的动物中,槟榔碱无法诱发θ波活动。已知胆碱能纤维释放的内源性乙酰胆碱可增加锥体细胞兴奋性。然而,在本研究中,静脉注射能诱发θ波活动剂量的氧化震颤素、槟榔碱和毒扁豆碱,会以剂量依赖的方式降低CA1锥体细胞的兴奋性,这是通过群体锋电位和树突兴奋性突触后电位幅度的降低来判断的。这些抑制作用可被东莨菪碱减弱,但不能被甲基东莨菪碱减弱。在中隔内侧区域有广泛损伤的大鼠中,槟榔碱的抑制作用减弱。本研究结果表明,外源性给予的拟胆碱药仅部分模拟内源性乙酰胆碱在海马体中的作用。外源性给予的拟胆碱药介导θ波活动和改变锥体细胞兴奋性的中枢作用位点仍有待阐明。

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