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Classification of muscarinic responses in hippocampus in terms of receptor subtypes and second-messenger systems: electrophysiological studies in vitro

机译:根据受体亚型和第二信使系统对海马毒蕈碱反应的分类:体外电生理研究

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摘要

The hippocampal slice preparation was used to classify cholinergic effects in terms of muscarinic receptor subtypes (M1 or M2) and biochemical effector systems linked to these effects in CA1 pyramidal cells. Based on the action of the M1 antagonist pirenzepine and the M2 antagonist gallamine, the muscarinic-induced membrane depolarization and blockade of the afterhyperpolarization appear to result from activation of an M1 receptor, while the cholinergic depression of the EPSP and the blockade of a potassium current termed the M-current appears to involve the activation of an M2 receptor. All of the muscarinic actions could be observed in pertussis toxin-treated hippocampi, suggesting that a pertussis toxin-sensitive G-protein is not involved in these actions. Cholinergic agents that are weak agonists of phosphoinositide (PI) turnover are fully effective in all of the muscarinic actions except the blockade of the M-current on which they had little agonist activity and actually blocked the action of full agonists. These results strongly suggest that the blockade of the M-current may involve stimulation of PI turnover. In addition, we show that the blockade of the M-current is mimicked by intracellular application of inositol trisphosphate. Our results do not show any obvious relationship between the muscarinic receptor subtypes and the biochemical effector systems.
机译:海马切片制剂用于根据毒蕈碱受体亚型(M1或M2)以及与CA1锥体细胞中与这些作用相关的生化效应系统对胆碱能作用进行分类。基于M1拮抗剂哌仑西平和M2拮抗剂没食子碱的作用,毒蕈碱诱导的膜去极化和超极化后阻滞似乎是由M1受体的激活引起的,而EPSP的胆碱能下降和钾电流的阻滞所谓的M电流似乎涉及M2受体的激活。在百日咳毒素治疗的海马中可以观察到所有毒蕈碱作用,这表明百日咳毒素敏感的G蛋白不参与这些作用。胆碱能药物是磷酸肌醇(PI)转换的弱激动剂,在所有毒蕈碱作用中都完全有效,除了对M电流的阻断作用外,它们对其几乎没有激动剂活性,而实际上阻止了完全激动剂的作用。这些结果强烈表明,M电流的阻断可能涉及刺激PI转换。此外,我们表明肌内三磷酸肌醇的细胞内应用模仿了M电流的封锁。我们的结果未显示毒蕈碱受体亚型与生化效应系统之间有任何明显的关系。

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