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μ阿片受体:钾离子电导的配体依赖性激活、脱敏及内化

mu-Opioid receptors: Ligand-dependent activation of potassium conductance, desensitization, and internalization.

作者信息

Alvarez Veronica A, Arttamangkul Seksiri, Dang Vu, Salem Abdallah, Whistler Jennifer L, Von Zastrow Mark, Grandy David K, Williams John T

机构信息

Vollum Institute and Department of Physiology and Pharmacology, Oregon Health and Sciences University, Portland, Oregon 97201, USA.

出版信息

J Neurosci. 2002 Jul 1;22(13):5769-76. doi: 10.1523/JNEUROSCI.22-13-05769.2002.

Abstract

micro-Opioid receptor (MOR) desensitization and endocytosis have been implicated in tolerance and dependence to opioids. The efficiency of each process is known to be agonist dependent; however, it is not known what determines the relative efficiency of various agonists at either process. In the present study, homologous MOR desensitization in locus ceruleus (LC) neurons and MOR internalization in HEK293 cells were examined using a series of agonists. The results show that the rank order of this series of agonists was different when comparing the magnitude of hyperpolarization and the ability to cause desensitization in LC neurons. Endocytosis of MOR was also examined in HEK293 cells using the same agonists. The relative ability to cause endocytosis in HEK293 cells correlated with the degree of desensitization in LC cells. This strong correlation suggests that the two processes are closely linked. The results also suggest that agonist efficacy is not necessarily a predictor of the ability to cause MOR desensitization or endocytosis. Identification and characterization of the biophysical properties of agonists that favor desensitization and internalization of receptors will lead to a better understanding of opioid signaling.

摘要

微阿片受体(MOR)脱敏和内吞作用与阿片类药物耐受性和依赖性有关。已知每个过程的效率取决于激动剂;然而,尚不清楚是什么决定了各种激动剂在任一过程中的相对效率。在本研究中,使用一系列激动剂检测了蓝斑(LC)神经元中的同源MOR脱敏和HEK293细胞中的MOR内化。结果表明,在比较超极化幅度和在LC神经元中引起脱敏的能力时,这一系列激动剂的排序不同。还使用相同的激动剂在HEK293细胞中检测了MOR的内吞作用。在HEK293细胞中引起内吞作用的相对能力与LC细胞中的脱敏程度相关。这种强相关性表明这两个过程紧密相连。结果还表明,激动剂效力不一定是引起MOR脱敏或内吞作用能力的预测指标。鉴定和表征有利于受体脱敏和内化的激动剂的生物物理特性将有助于更好地理解阿片类信号传导。

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