The role of MK-801 in sensitization to stimulants

被引:31
作者
Sripada, S
Gaytan, O
Swann, A
Dafny, N
机构
[1] Univ Texas, Sch Med, Dept Neurobiol & Anat, Houston, TX 77225 USA
[2] Univ Texas, Sch Med, Dept Psychiat & Behav Sci, Houston, TX 77225 USA
关键词
MK-801; psychomotor stimulant; motor effect; behavioral sensitization; conditioning; state-dependent learning; amphetamine; cocaine; methylphenidate;
D O I
10.1016/S0165-0173(00)00046-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Behavioral responses to stimulants can be progressively and persistently enhanced by their repeated administration. This phenomenon, called behavioral sensitization, may underlie substance abuse, psychosis, recurrence in bipolar disorder, or other psychiatric problems. A growing body of work has implicated excitatory amino acid systems in behavioral sensitization. Most of the evidence for a role of excitatory amino acids has come from experiments demonstrating prevention of sensitization by excitatory amino acid antagonists, especially the noncompetitive NMDA receptor antagonist MK-801. Results of studies with MK-801 have varied, however, leading to conflicting interpretations of its relationship to behavioral sensitization. This paper critically discusses the design of experiments that have used MK-801, and interprets data from these experiments in terms of the two leading explanations for the role of MK-801: 1) that sensitization is an example of the family of plastic events that require excitatory amino acid transmission or 2) that interoceptive cues associated with MK-801 lead to state-dependent learning that modifies sensitization because, in essence, the animal does not recognize the stimulant as the same drug if it is given in close association with MK-801. Based on conflicting reports on effects of MK-801, we propose 1) strategies for distinguishing components of MK-801's effects on responses to stimulants, 2) a model that is a hybrid of the two interpretations of its effects on sensitization, and 3) experimental strategies for testing this model. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 114
页数:18
相关论文
共 95 条
[11]   The 5-HT2A receptor antagonist M100907 is more effective in counteracting NMDA antagonist than dopamine agonist induced hyperactivity in mice [J].
Carlsson, ML ;
Martin, P ;
Nilsson, M ;
Sorensen, SM ;
Carlsson, A ;
Waters, S ;
Waters, N .
JOURNAL OF NEURAL TRANSMISSION, 1999, 106 (02) :123-129
[12]   Effects of dopaminergic and glutamatergic receptor antagonists on the establishment and expression of conditioned locomotion to cocaine in rats [J].
Cervo, L ;
Samanin, R .
BRAIN RESEARCH, 1996, 731 (1-2) :31-38
[13]   A STUDY OF ALCOHOL-TOLERANCE EFFECT AND AN INTRODUCTION OF A NEW BEHAVIOURAL TECHNIQUE [J].
CHEN, CS .
PSYCHOPHARMACOLOGIA, 1968, 12 (05) :433-&
[14]   Multiple within-day conflict testing to define the time course of anxiolytic drug effects [J].
Commissaris, RL ;
Xie, ZC ;
Ninichuk, PJ ;
Markovska, VL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1996, 53 (02) :369-377
[15]  
CONGER JJ, 1951, Q J STUD ALCOHOL, V12, P1
[16]   ABSENCE OF ENVIRONMENT-SPECIFICITY IN MORPHINE-TOLERANCE ACQUIRED IN NON-DISTINCTIVE ENVIRONMENTS - HABITUATION OR STIMULUS OVERSHADOWING [J].
DAFTERS, R ;
BACH, L .
PSYCHOPHARMACOLOGY, 1985, 87 (01) :101-106
[17]   THE NMDA ANTAGONIST MK-801 CAN IMPAIR ATTENTION TO EXTEROCEPTIVE STIMULI [J].
DAI, HL ;
CAREY, RJ .
BEHAVIOURAL BRAIN RESEARCH, 1994, 62 (02) :149-156
[18]   TIME-COURSE EFFECTS OF MK-801 - THE RELATIONSHIP BETWEEN BRAIN NEUROCHEMISTRY AND BEHAVIOR [J].
DAI, HL ;
GEBHARDT, K ;
CAREY, RJ .
BRAIN RESEARCH BULLETIN, 1995, 36 (02) :175-180
[19]   The non-competitive NMDA receptor blocker dizocilpine potentiates serotonergic function [J].
Dall'Olio, R ;
Gaggi, R ;
Bonfante, V ;
Gandolfi, O .
BEHAVIOURAL PHARMACOLOGY, 1999, 10 (01) :63-71
[20]   EFFECT OF CHRONIC TREATMENT WITH DIZOCILPINE (MK-801) ON THE BEHAVIORAL-RESPONSE TO DOPAMINE RECEPTOR AGONISTS IN THE RAT [J].
DALLOLIO, R ;
GANDOLFI, O ;
MONTANARO, N .
PSYCHOPHARMACOLOGY, 1992, 107 (04) :591-594