Explaining the escalation of drug use in substance dependence:: Models and appropriate animal laboratory tests

被引:100
作者
Zernig, Gerald
Ahmed, Serge H.
Cardinal, Rudolf N.
Morgan, Drake
Acquas, Elio
Foltin, Richard W.
Vezina, Paul
Negus, S. Stevens
Crespo, Jose A.
Stoeckl, Petra
Grubinger, Petra
Madlung, Ekkehard
Haring, Christian
Kurz, Martin
Saria, Alois
机构
[1] Med Univ Innsbruck, Dept Psychiat, Expt Psychiat Unit, A-6020 Innsbruck, Austria
[2] Med Univ Innsbruck, Substance Abuse Treatment Ctr, A-6020 Innsbruck, Austria
[3] Psychiat Hosp Tirol, Primariat B, Tyrol, Austria
[4] Univ Bordeaux 2, CNRS, UMR 5227, F-33076 Bordeaux, France
[5] Univ Cambridge, Dept Expt Psychol, Cambridge CB2 1TN, England
[6] Univ Florida, Coll Med, Dept Psychiat, Div Addict Med, Gainesville, FL 32611 USA
[7] Columbia Univ, New York State Psychiat Inst, Dept Psychiat, New York, NY 10027 USA
[8] Univ Chicago, Dept Psychiat, Chicago, IL 60637 USA
[9] Harvard Univ, McLean Hosp, Alcohol & Drug Abuse Res Ctr, Belmont, MA 02178 USA
[10] Univ Cagliari, Dept Toxicol, I-09124 Cagliari, Italy
[11] Univ Cagliari, Ctr Excellence Neurobiol Addict, I-09124 Cagliari, Italy
关键词
alcohol; amphetamine; baboon; clinical trial; cocaine; cognitive behavioral therapy; conditioned stimulus strength; drug abuse; drug dependence; habit formation; hedonic value; heroin; human; incentive salience; incentive value; methylenedioxymethamphetamine; morphine; nicotine; opioids; psychoanalysis; psychostimulants; psychotherapy; rat; rhesus monkey; remifentanil; review; reward allostasis; self-administration; sensitization; squirrel monkey; subjective effect; tolerance;
D O I
10.1159/000103923
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Escalation of drug use, a hallmark of drug dependence, has traditionally been interpreted as reflecting the development of tolerance to the drug's effects. However, on the basis of animal behavioral data, several groups have recently proposed alternative explanations, i.e. that such an escalation of drug use might not be based on ( 1) tolerance, but rather be indicative of (2) sensitization to the drug's reinforcing effect, 3) reward allostasis, ( 4) an increase in the incentive salience of drug-associated stimuli, ( 5) an increase in the reinforcing strength of the drug reinforcer relative to alternative reinforcers, or ( 6) habit formation. From the pharmacological perspective, models 1-3 allow predictions about the change in the shape of drug dose-effect curves that are based on mathematically defined models governing receptor-ligand interaction and signal transduction. These predictions are tested in the present review, which also describes the other currently championed models for drug use escalation and other components of apparent 'reinforcement' (in its original meaning, like 'tolerance' or 'sensitization', a purely descriptive term). It evaluates the animal experimental approaches employed to support or prove the existence of each of the models and reinforcement components, and recapitulates the clinical evidence, which strongly suggests that escalation of drug use is predominantly based on an increase in the frequency of intoxication events rather than an increase in the dose taken at each intoxication event. Two apparent discrepancies in animal experiments are that ( a) sensitization to overall reinforcement has been found more often for psychostimulants than for opioids, and that (b) tolerance to the reinforcing and other effects has been observed more often for opioids than for cocaine. These discrepancies are resolved by the finding that cocaine levels seem to be more tightly regulated at submaximum reinforcing levels than opioid levels are. Consequently, animals self-administering opioids are more likely to expose themselves to higher above-threshold doses than animals self-administering psychostimulants, rendering the development of tolerance to opioids more likely than tolerance to psychostimulants. The review concludes by making suggestions on how to improve the current behavioral experimental approaches. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:65 / 119
页数:55
相关论文
共 268 条
[1]   DEPRESSION OF MESOLIMBIC DOPAMINE TRANSMISSION AND SENSITIZATION TO MORPHINE DURING OPIATE ABSTINENCE [J].
ACQUAS, E ;
DICHIARA, G .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1620-1625
[2]   Mood disorders in opioid-dependent patients [J].
Ahmadi, J ;
Majdi, B ;
Mahdavi, S ;
Mohagheghzadeh, M .
JOURNAL OF AFFECTIVE DISORDERS, 2004, 82 (01) :139-142
[3]   Imbalance between drug and non-drug reward availability: A major risk factor for addiction [J].
Ahmed, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 526 (1-3) :9-20
[4]   Transition to drug addiction: a negative reinforcement model based on an allostatic decrease in reward function [J].
Ahmed, SH ;
Koob, GF .
PSYCHOPHARMACOLOGY, 2005, 180 (03) :473-490
[5]   Transition from moderate to excessive drug intake: Change in hedonic set point [J].
Ahmed, SH ;
Koob, GF .
SCIENCE, 1998, 282 (5387) :298-300
[6]   Neuroscience - Addiction as compulsive reward prediction [J].
Ahmed, SH .
SCIENCE, 2004, 306 (5703) :1901-1902
[7]   Vertical shifts in dose-injection curves reflect reward allostasis, not sensitization - Reply [J].
Ahmed, SH ;
Koob, GF .
PSYCHOPHARMACOLOGY, 2004, 171 (03) :354-355
[8]   Escalation of cocaine self-administration does not depend on altered cocaine-induced nucleus accumbens dopamine levels [J].
Ahmed, SH ;
Lin, D ;
Koob, GF ;
Parsons, LH .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (01) :102-113
[9]   Neurobiological evidence for hedonic allostasis associated with escalating cocaine use [J].
Ahmed S.H. ;
Kenny P.J. ;
Koob G.F. ;
Markou A. .
Nature Neuroscience, 2002, 5 (7) :625-626
[10]   SOCIAL-LEARNING AND DEVIANT-BEHAVIOR - SPECIFIC TEST OF A GENERAL-THEORY [J].
AKERS, RL ;
KROHN, MD ;
LANZAKADUCE, L ;
RADOSEVICH, M .
AMERICAN SOCIOLOGICAL REVIEW, 1979, 44 (04) :636-655