Differential desensitization of human δ-opioid receptors by peptide and alkaloid agonists

被引:27
作者
Allouche, S [1 ]
Roussel, M [1 ]
Marie, N [1 ]
Jauzac, P [1 ]
机构
[1] Univ Caen, CHU Cote Nacre, Lab Biochem A, F-14033 Caen, France
关键词
delta-opioid receptor; alkaloid agonist; peptide agonist; desensitization; adenylyl cyclase inhibition;
D O I
10.1016/S0014-2999(99)00180-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The efficacy of different opioid agonists to induce acute desensitization of the human delta-opioid receptor-mediated inhibition of cAMP accumulation was investigated in the neuroblastoma cell line SK-N-BE, which endogenously expresses these receptors. While etorphine, a non-selective alkaloid agonist, caused 50% desensitization after a 30-min incubation, the same treatment in the presence of the selective peptide agonists, DPDPE ([D-Pen(2),D-Pen(5)]enkephalin) and deltorphin I (Tyr-D-Ala-Phe-Asp-Val-Val-Gly), almost totally desensitized the delta-opioid receptor-mediated inhibition of adenylyl cyclase. When SK-N-BE cells were prechallenged either with alkaloid or peptide agonist, we observed a cross-desensitization that was less marked when cells were pretreated with peptide agonists and then challenged with etorphine. Taken together, these results demonstrate that human delta-opioid receptors are differentially desensitized by alkaloid and peptide agonists. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:235 / 240
页数:6
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