Differential behavioral and molecular alterations upon protracted abstinence from cocaine versus morphine, nicotine, THC and alcohol

被引:47
作者
Becker, Jerome A. J. [1 ,2 ]
Kieffer, Brigitte L. [1 ,3 ]
Le Merrer, Julie [1 ,2 ]
机构
[1] Univ Strasbourg, Inst Genet & Biol Mol & Cellulaire, Med Translat & Neurogenet, INSERM U 964,CNRS UMR 7104, F-67400 Illkirch Graffenstaden, France
[2] Univ Tours Rabelais, Physiol Reprod & Comportements, INRA UMR 0085, CNRS UMR 7247, F-37380 Nouzilly, France
[3] McGill Univ, Fac Med, Dept Psychiat, Douglas Hosp Res Ctr, Montreal, PQ, Canada
基金
美国国家卫生研究院;
关键词
extended amygdala; gene expression; social interaction; NUCLEUS-ACCUMBENS CORE; ANXIETY-LIKE BEHAVIOR; MEDIUM SPINY NEURONS; DENDRITIC MORPHOLOGY; ETHANOL EXPOSURE; OPIOID-RECEPTORS; NEURAL CIRCUITS; WITHDRAWAL; ADDICTION; HEROIN;
D O I
10.1111/adb.12405
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
Unified theories of addiction are challenged by differing drug-seeking behaviors and neurobiological adaptations across drug classes, particularly for narcotics and psychostimulants. We previously showed that protracted abstinence to opiates leads to despair behavior and social withdrawal in mice, and we identified a transcriptional signature in the extended amygdala that was also present in animals abstinent from nicotine, Delta 9-tetrahydrocannabinol (THC) and alcohol. Here we examined whether protracted abstinence to these four drugs would also share common behavioral features, and eventually differ from abstinence to the prototypic psychostimulant cocaine. We found similar reduced social recognition, increased motor stereotypies and increased anxiety with relevant c-fos response alterations in morphine, nicotine, THC and alcohol abstinent mice. Protracted abstinence to cocaine, however, led to strikingly distinct, mostly opposing adaptations at all levels, including behavioral responses, neuronal activation and gene expression. Together, these data further document the existence of common hallmarks for protracted abstinence to opiates, nicotine, THC and alcohol that develop within motivation/emotion brain circuits. In our model, however, these do not apply to cocaine, supporting the notion of unique mechanisms in psychostimulant abuse.
引用
收藏
页码:1205 / 1217
页数:13
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