Drug-induced alterations in the extracellular signal-regulated kinase (ERK) signalling pathway: Implications for reinforcement and reinstatement

被引:74
作者
Zhai, Haifeng [1 ]
Li, Yanqin [1 ]
Wang, Xi [1 ]
Lu, Lin [1 ]
机构
[1] Peking Univ, Dept Neuropharmacol, Natl Inst Drug Dependence, Beijing 100083, Peoples R China
关键词
addiction; neuroplasticity; reward; relapse; dopamine; glutamate; contextual cues;
D O I
10.1007/s10571-007-9240-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Drug addiction, characterized by high rates of relapse, is recognized as a kind of neuroadaptive disorder. Since the extracellular signal-regulated kinase (ERK) pathway is critical to neuroplasticity in the adult brain, understanding the role this pathway plays is important for understanding the molecular mechanism underlying drug addiction and relapse. Here, we review previous literatures that focus on the effects of exposure to cocaine, amphetamine, Delta(9)-tetrahydrocannabinol (THC), nicotine, morphine, and alcohol on ERK signaling in the mesocorticolimbic dopamine system; these alterations of ERK signaling have been thought to contribute to the drug's rewarding effects and to the long-term maladaptation induced by drug abuse. We then discuss the possible upstreams of the ERK signaling pathway activated by exposure of drugs of abuse and the environmental cues previously paired with drugs. Finally, we argue that since ERK activation is a key molecular process in reinstatement of conditioned place preference and drug self-administration, the pharmacological manipulation of the ERK pathway is a potential treatment strategy for drug addiction.
引用
收藏
页码:157 / 172
页数:16
相关论文
共 77 条
[1]   cAMP cascade leads to Ras activation in cortical neurons [J].
Ambrosini, A ;
Tininini, S ;
Barassi, A ;
Racagni, G ;
Sturani, E ;
Zippel, R .
MOLECULAR BRAIN RESEARCH, 2000, 75 (01) :54-60
[2]  
Berhow MT, 1996, J NEUROSCI, V16, P4707
[3]   Regulation of the extracellular signal-regulated kinases following acute and chronic opioid treatment [J].
Bilecki, W ;
Zapart, G ;
Ligeza, A ;
Wawrzczak-Bargiela, A ;
Urbanski, MJ ;
Przewlocki, R .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (19-20) :2369-2375
[4]  
Bontempi B, 1997, J NEUROSCI, V17, P8596
[5]   Parsing molecular and behavioral effects of cocaine in mitogen- and stress-activated protein kinase-1-deficient mice [J].
Brami-Cherrier, K ;
Valjent, E ;
Hervé, D ;
Darragh, J ;
Corvol, JC ;
Pages, C ;
Simon, AJ ;
Girault, JA ;
Caboche, J .
JOURNAL OF NEUROSCIENCE, 2005, 25 (49) :11444-11454
[6]   In vivo nicotine treatment regulates mesocorticolimbic CREB and ERK signaling in C57Bl/6J mice [J].
Brunzell, DH ;
Russell, DS ;
Picciotto, MR .
JOURNAL OF NEUROCHEMISTRY, 2003, 84 (06) :1431-1441
[7]   Drug addiction [J].
Camí, J ;
Farré, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (10) :975-986
[8]   Acute ethanol inhibits extracellular signal-regulated kinase, protein kinase B, and adenosine 3′:5′-cyclic monophosphate response element binding protein activity in an age- and brain region-speciric manner [J].
Chandler, LJ ;
Sutton, G .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (04) :672-682
[9]   CaMKII regulates amphetamine-induced ERKI/2 phosphorylation in striatal neurons [J].
Choe, ES ;
Wang, JQ .
NEUROREPORT, 2002, 13 (08) :1013-1016
[10]  
Choe ES, 2002, NEUROPSYCHOPHARMACOL, V27, P565