神经元毒蕈碱受体敏感性调控的分子机制。

E E el-Fakahany, C L Cioffi
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引用次数: 30

摘要

与其他神经递质受体一样,毒蕈碱乙酰胆碱受体受受体激活状态的调节。在体内和体外,毒蕈碱激动剂浓度的长期增加导致受体密度的降低和受体敏感性的丧失。另一方面,当受体在体内长时间被剥夺乙酰胆碱时,受体对毒蕈碱激动剂的反应变得更加敏感。然而,要证明伴随这种超敏感状态的受体浓度的增加是比较困难的。这篇综述的目的是提供有关毒蕈碱受体调节的特征和这种现象背后的分子机制的最新信息,包括受体的密度和它们的转导机制。此外,还讨论了不同第二信使信号可能的反馈调节作用。特别强调致力于神经毒蕈碱受体调节的分子机制。
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Molecular mechanisms of regulation of neuronal muscarinic receptor sensitivity.

Like other neurotransmitter receptors, muscarinic acetylcholine receptors are subject to regulation by the state of receptor activation. Prolonged increases in the concentration of muscarinic agonists result in a decrease in receptor density and loss of receptor sensitivity, both in vivo and in vitro. On the other hand, when the receptor is deprived of acetylcholine for a long duration in vivo, the receptor becomes more sensitive in responding to muscarinic agonists. However, it has been more difficult to demonstrate increases in receptor concentration that accompany this supersensitive state. The purpose of this review is to provide current information related to the characteristics of muscarinic receptor regulation and the molecular mechanisms underlying this phenomenon, regarding both the density of receptors and their transduction mechanisms. Furthermore, possible feedback regulatory roles of different second messenger signals are discussed. Particular emphasis is dedicated to molecular mechanisms of regulation of neuronal muscarinic receptors.

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