Opioid receptors

被引:598
作者
Waldhoer, M [1 ]
Bartlett, SE [1 ]
Whistler, JL [1 ]
机构
[1] Univ Calif San Francisco, Ernest Gallo Clin & Res Ctr, Emeryville, CA 94608 USA
关键词
morphine; GPCR/7TM; RAVE; tolerance; dependence;
D O I
10.1146/annurev.biochem.73.011303.073940
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Opioid receptors belong to the large superfamily of seven transmembrane-spanning (7TM) G protein-coupled receptors (GPCRs). As a class, GPCRs are of fundamental physiological importance mediating the actions of the majority of known neurotransmitters and hormones. Opioid receptors are particularly intriguing members of this receptor family. They are activated both by endogenously produced opioid peptides and by exogenously administered opiate compounds, some of which are not only among the most effective analgesics known but also highly addictive drugs of abuse. A fundamental question in addiction biology is why exogenous opioid drugs, such as morphine and heroin, have a high liability for inducing tolerance, dependence, and addiction. This review focuses on many aspects of opioid receptors with the aim of gaining a greater insight into mechanisms of opioid tolerance and dependence.
引用
收藏
页码:953 / 990
页数:38
相关论文
共 307 条
[111]   AGONISTS AND ANTAGONISTS BIND TO DIFFERENT DOMAINS OF THE CLONED KAPPA-OPIOID RECEPTOR [J].
KONG, HY ;
RAYNOR, K ;
YANO, H ;
TAKEDA, J ;
BELL, GI ;
REISINE, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :8042-8046
[112]  
KONG HY, 1993, J BIOL CHEM, V268, P23055
[113]   Drug addiction, dysregulation of reward, and allostasis [J].
Koob, GF ;
Le Moal, M .
NEUROPSYCHOPHARMACOLOGY, 2001, 24 (02) :97-129
[114]   NEURAL SUBSTRATES OF OPIATE WITHDRAWAL [J].
KOOB, GF ;
MALDONADO, R ;
STINUS, L .
TRENDS IN NEUROSCIENCES, 1992, 15 (05) :186-191
[115]   Targeted disruption of the orphanin FQ/nociceptin gene increases stress susceptibility and impairs stress adaptation in mice [J].
Köster, A ;
Montkowski, A ;
Schulz, S ;
Stübe, EM ;
Knaudt, K ;
Jenck, F ;
Moreau, JL ;
Nothacker, HP ;
Civelli, O ;
Reinscheid, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (18) :10444-10449
[116]  
Kovoor A, 1998, MOL PHARMACOL, V54, P704
[117]   mu and delta opioid receptors are differentially desensitized by the coexpression of beta-adrenergic receptor kinase 2 and beta-arrestin 2 in Xenopus oocytes [J].
Kovoor, A ;
Nappey, V ;
Kieffer, BL ;
Chavkin, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :27605-27611
[118]   Mutation of tyrosine 318 (Y318F) in the delta-opioid receptor attenuates tyrosine phosphorylation, agonist-dependent receptor internalization, and mitogen-activated protein kinase activation [J].
Kramer, HK ;
Andria, ML ;
Kushner, SA ;
Esposito, DH ;
Hiller, JM ;
Simon, EJ .
MOLECULAR BRAIN RESEARCH, 2000, 79 (1-2) :55-66
[119]   Tyrosine phosphorylation of the δ-opioid receptor -: Evidence for its role in mitogen-activated protein kinase activation and receptor internalization [J].
Kramer, HK ;
Andria, ML ;
Esposito, DH ;
Simon, EJ .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (06) :781-792
[120]   The role of receptor kinases and arrestins in G protein-coupled receptor regulation [J].
Krupnick, JG ;
Benovic, JL .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1998, 38 :289-319