Suppr超能文献

功能性μ阿片受体脱敏增加激动剂的失活速率。

Desensitization of functional µ-opioid receptors increases agonist off-rate.

机构信息

Vollum Institute, Oregon Health and Science University, Portland, Oregon

出版信息

Mol Pharmacol. 2014 Jul;86(1):52-61. doi: 10.1124/mol.114.092098. Epub 2014 Apr 18.

Abstract

Desensitization of µ-opioid receptors (MORs) develops over 5-15 minutes after the application of some, but not all, opioid agonists and lasts for tens of minutes after agonist removal. The decrease in function is receptor selective (homologous) and could result from 1) a reduction in receptor number or 2) a decrease in receptor coupling. The present investigation used photolysis of two caged opioid ligands to examine the kinetics of MOR-induced potassium conductance before and after MOR desensitization. Photolysis of a caged antagonist, carboxynitroveratryl-naloxone (caged naloxone), blocked the current induced by a series of agonists, and the time constant of decline was significantly decreased after desensitization. The increase in the rate of current decay was not observed after partial blockade of receptors with the irreversible antagonist, β-chlornaltrexamine (β-CNA). The time constant of current decay after desensitization was never more rapid than 1 second, suggesting an increased agonist off-rate rather than an increase in the rate of channel closure downstream of the receptor. The rate of G protein-coupled K(+) channel (GIRK) current activation was examined using photolysis of a caged agonist, carboxynitrobenzyl-tyrosine-[Leu(5)]-enkephalin. After acute desensitization or partial irreversible block of MORs with β-CNA, there was an increase in the time it took to reach a peak current. The decrease in the rate of agonist-induced GIRK conductance was receptor selective and dependent on receptor number. The results indicate that opioid receptor desensitization reduced the number of functional receptor and that the remaining active receptors have a reduced agonist affinity.

摘要

μ-阿片受体(MOR)脱敏在某些但不是所有阿片激动剂应用后 5-15 分钟发生,并在激动剂去除后持续数十分钟。功能下降是受体选择性的(同源的),可能是由于 1)受体数量减少或 2)受体偶联减少。本研究使用两种笼状阿片配体的光解来研究 MOR 脱敏前后 MOR 诱导钾电导的动力学。笼状拮抗剂羧基硝基香草基-纳洛酮(笼状纳洛酮)的光解阻断了一系列激动剂诱导的电流,脱敏后下降的时间常数显著降低。不可逆拮抗剂β-氯纳曲酮(β-CNA)部分阻断受体后,没有观察到电流衰减率的增加。电流衰减后的时间常数从未快于 1 秒,这表明激动剂的脱靶率增加,而不是受体下游通道关闭的速度增加。使用笼状激动剂羧基硝基苄基-酪氨酸-[亮氨酸(5)]-脑啡肽的光解来检查 G 蛋白偶联 K(+)通道(GIRK)电流的激活速率。急性脱敏或β-CNA 对 MOR 进行部分不可逆阻断后,达到峰值电流所需的时间增加。激动剂诱导的 GIRK 电导的降低是受体选择性的,取决于受体数量。结果表明,阿片受体脱敏减少了功能性受体的数量,并且剩余的活性受体对激动剂的亲和力降低。

相似文献

引用本文的文献

1
A Chemically Stable Photocaged Noradrenaline.一种化学稳定的光笼去甲肾上腺素。
ACS Chem Neurosci. 2025 Aug 6;16(15):2935-2944. doi: 10.1021/acschemneuro.5c00241. Epub 2025 Jul 8.
2
In vivo photopharmacology with light-activated opioid drugs.体内光药理学与光激活阿片类药物。
Neuron. 2023 Dec 20;111(24):3926-3940.e10. doi: 10.1016/j.neuron.2023.09.017. Epub 2023 Oct 16.

本文引用的文献

1
Caged naloxone reveals opioid signaling deactivation kinetics.笼内纳洛酮揭示阿片类信号失活动力学。
Mol Pharmacol. 2013 Nov;84(5):687-95. doi: 10.1124/mol.113.088096. Epub 2013 Aug 19.
5
GIRK channel modulation by assembly with allosterically regulated RGS proteins.GIRK 通道通过与变构调节的 RGS 蛋白组装进行调节。
Proc Natl Acad Sci U S A. 2012 Dec 4;109(49):19977-82. doi: 10.1073/pnas.1214337109. Epub 2012 Nov 19.
6
μ-Opioid receptor desensitization: homologous or heterologous?μ-阿片受体脱敏:同源还是异源?
Eur J Neurosci. 2012 Dec;36(12):3636-42. doi: 10.1111/ejn.12003. Epub 2012 Sep 24.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验