Arttamangkul Seksiri, Torrecilla Maria, Kobayashi Kazuto, Okano Hideyuki, Williams John T
Vollum Institute, Oregon Health and Science University, Portland, Oregon 97239, USA.
J Neurosci. 2006 Apr 12;26(15):4118-25. doi: 10.1523/JNEUROSCI.0303-06.2006.
A close relationship between desensitization and internalization of mu-opioid receptors (MORs) has been proposed based on differential actions of series of agonists. The role that these two processes have in the development of tolerance and dependence to opioids has been a controversial subject that has been studied in a variety of model systems. Here, we examine desensitization and internalization of endogenous MORs simultaneously in primary cultures of locus ceruleus neurons using fluorescently tagged peptide agonists. With the use of two fluorescent opioid peptides, dermorphin-Bodipy Texas Red and dermorphin-Alexa594 (Derm-A594), desensitization was measured electrophysiologically and trafficking was followed by the accumulation of intracellular fluorescent puncta. Blocking endocytosis with concanavalin A eliminated the accumulation of fluorescent puncta but desensitization induced by Derm-A594 was unaffected. Likewise, after treatment with concanavalin A, there was no change in either desensitization or recovery from desensitization induced by [Met]5enkephalin. The results demonstrate that desensitization and the recovery from desensitization are not dependent on receptor internalization and suggest that the activity of endogenous MORs in primary neurons can be modulated at the level of the plasma membrane.
基于一系列激动剂的不同作用,有人提出了μ-阿片受体(MORs)脱敏与内化之间的密切关系。这两个过程在阿片类药物耐受性和依赖性发展中所起的作用一直是一个有争议的话题,已在多种模型系统中进行了研究。在这里,我们使用荧光标记的肽激动剂,在蓝斑神经元的原代培养物中同时检测内源性MORs的脱敏和内化。通过使用两种荧光阿片肽,德莫啡肽-硼二吡咯烷 Texas红和德莫啡肽- Alexa594(Derm-A594),通过电生理学方法测量脱敏,通过细胞内荧光斑点的积累追踪转运。用伴刀豆球蛋白A阻断内吞作用消除了荧光斑点的积累,但Derm-A594诱导的脱敏不受影响。同样,在用伴刀豆球蛋白A处理后,[Met]5脑啡肽诱导的脱敏或脱敏恢复均无变化。结果表明,脱敏和脱敏恢复不依赖于受体内化,提示原代神经元中内源性MORs的活性可在质膜水平上受到调节。