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烟碱型乙酰胆碱受体的脱敏:分子机制及调节剂的作用

Desensitization of the nicotinic acetylcholine receptor: molecular mechanisms and effect of modulators.

作者信息

Ochoa E L, Chattopadhyay A, McNamee M G

机构信息

Department of Biochemistry and Biophysics, University of California, Davis 95616.

出版信息

Cell Mol Neurobiol. 1989 Jun;9(2):141-78. doi: 10.1007/BF00713026.

DOI:10.1007/BF00713026
PMID:2663167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11567434/
Abstract
  1. Loss of response after prolonged or repeated application of stimulus is generally termed desensitization. A wide variety of phenomena occurring in living organisms falls under this general definition of desensitization. There are two main types of desensitization processes: specific and non-specific. 2. Desensitization of the nicotinic acetylcholine receptor is triggered by prolonged or repeated exposure to agonists and results in inactivation of its ion channel. It is a case of specific desensitization and is an intrinsic molecular property of the receptor. 3. Desensitization of the nicotinic acetylcholine receptor at the neuromuscular junction was first reported by Katz and Thesleff in 1957. Desensitization of the receptor has been demonstrated by rapid kinetic techniques and also by the characteristic "burst kinetics" obtained from single-channel recordings of receptor activity in native as well as in reconstituted membranes. In spite of a number of studies, the detailed molecular mechanism of the nicotinic acetylcholine receptor desensitization is not known with certainty. The progress of desensitization is accompanied by an increase in affinity of the receptor for its agonist. This change in affinity is attributed to a conformational change of the receptor, as detected by spectroscopic and kinetic studies. A four-state general model is consistent with the major experimental observations. 4. Desensitization of the nicotinic acetylcholine receptor can be potentially modulated by exogenous and endogenous substances and by covalent modifications of the receptor structure. Modulators include the noncompetitive blockers, calcium, the thymic hormone peptides (thymopoietin and thymopentin), substance P, the calcitonin gene-related peptide, and receptor phosphorylation. Phosphorylation is an important posttranslational covalent modification that is correlated with the regulation and desensitization of the receptor through various protein kinases. 5. Although the physiological significance of desensitization of the nicotinic receptor is not yet fully understood, desensitization of receptors probably plays a significant role in the operation of the neuronal networks associated in memory and learning processes. Desensitization of the nicotinic receptor could also possibly be related to the neuromuscular disease, myasthenia gravis.
摘要
  1. 在长时间或重复施加刺激后反应丧失通常被称为脱敏。生物体中发生的各种各样的现象都属于这种脱敏的一般定义。脱敏过程主要有两种类型:特异性和非特异性。2. 烟碱型乙酰胆碱受体的脱敏是由长时间或重复暴露于激动剂引发的,并导致其离子通道失活。这是特异性脱敏的一个例子,是该受体的一种内在分子特性。3. 1957年,卡茨和泰斯莱夫首次报道了神经肌肉接头处烟碱型乙酰胆碱受体的脱敏。受体的脱敏已通过快速动力学技术以及从天然和重组膜中受体活性的单通道记录获得的特征性“爆发动力学”得到证实。尽管进行了大量研究,但烟碱型乙酰胆碱受体脱敏的详细分子机制仍不确定。脱敏过程伴随着受体对其激动剂亲和力的增加。这种亲和力的变化归因于受体的构象变化,这是通过光谱和动力学研究检测到的。一个四态通用模型与主要实验观察结果一致。4. 烟碱型乙酰胆碱受体的脱敏可能受到外源性和内源性物质以及受体结构的共价修饰的调节。调节剂包括非竞争性阻断剂、钙、胸腺激素肽(胸腺生成素和胸腺五肽)、P物质、降钙素基因相关肽以及受体磷酸化。磷酸化是一种重要的翻译后共价修饰,它通过各种蛋白激酶与受体的调节和脱敏相关。5. 尽管烟碱型受体脱敏的生理意义尚未完全理解,但受体脱敏可能在与记忆和学习过程相关的神经网络运作中发挥重要作用。烟碱型受体的脱敏也可能与神经肌肉疾病重症肌无力有关。