Cross-talk between the epigenome and neural circuits in drug addiction

被引:19
作者
Mews, Philipp [1 ]
Calipari, Erin S. [2 ]
机构
[1] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[2] Vanderbilt Univ, Sch Med, Vanderbilt Ctr Addict Res, Nashville, TN 37212 USA
来源
BRAIN RESEARCH IN ADDICTION | 2017年 / 235卷
关键词
Dopamine; Addiction; Reinforcement; Epigenetics; Circuits; INDUCED STRUCTURAL PLASTICITY; MESOLIMBIC DOPAMINE SYSTEM; MEDIUM SPINY NEURONS; LONG-TERM-MEMORY; NUCLEUS-ACCUMBENS DOPAMINE; HISTONE ACETYLATION; SYNAPTIC PLASTICITY; DENDRITIC SPINES; COCAINE-SEEKING; PREFRONTAL CORTEX;
D O I
10.1016/bs.pbr.2017.08.012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Drug addiction is a behavioral disorder characterized by dysregulated learning about drugs and associated cues that result in compulsive drug seeking and relapse. Learning about drug rewards and predictive cues is a complex process controlled by a computational network of neural connections interacting with transcriptional and molecular mechanisms within each cell to precisely guide behavior. The interplay between rapid, temporally specific neuronal activation, and longer-term changes in transcription is of critical importance in the expression of appropriate, or in the case of drug addiction, inappropriate behaviors. Thus, these factors and their interactions must be considered together, especially in the context of treatment. Understanding the complex interplay between epigenetic gene regulation and circuit connectivity will allow us to formulate novel therapies to normalize maladaptive reward behaviors, with a goal of modulating addictive behaviors, while leaving natural reward-associated behavior unaffected.
引用
收藏
页码:19 / 63
页数:45
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