The extinction of morphine-induced conditioned place preference by histone deacetylase inhibition

被引:41
作者
Wang, Ru [1 ]
Zhang, Yan [1 ]
Qing, Hua [1 ]
Liu, Mei [1 ]
Yang, Peng [1 ]
机构
[1] Fourth Mil Med Univ, Tangdu Hosp, Dept Pharm, Xian 710038, Shaanxi, Peoples R China
关键词
Extinction; Morphine; Conditioned place preference; Histone deacetylase inhibition; LONG-TERM-MEMORY; GENE-EXPRESSION; SYNAPTIC PLASTICITY; DRUG-ADDICTION; COCAINE; CREB; ACTIVATION; STRIATUM; AMYGDALA; PROTEIN;
D O I
10.1016/j.neulet.2010.07.080
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent evidence suggests that epigenetic mechanisms have an important role in the development of addictive behavior. However, little is known about the role of epigenetic mechanisms in the extinction of morphine-induced behavioral changes. In this study, we will examine the effect of histone deacetylase (HDAC) inhibitors on extinction of morphine-induced conditioned place preference (CPP). To facilitate extinction, rats will be administered an HDAC inhibitor (HDACi) following nonreinforced exposure to the conditioned context. To measure persistence, rats were subject to a reinstatement test using 3 mg/kg dose of morphine. To exclude the effect of repeated NaBut injections themselves on morphine-CPP in the absence of extinction session, rats received injection of either NaBut or vehicle for 8 days. We found that HDAC inhibition during nonconfined extinction or confined extinction consolidation can facilitate extinction of morphine-induced CPP. We also showed that the extinction of drug seeking via HDAC inhibition modulates extinction learning such that reinstatement behavior is significantly attenuated. There is no effect of repeated NaBut injections themselves on morphine-CPP in the absence of extinction session. In conclusion, our results extend earlier reports on the ability of HDACi to modify the behavioral effects of drugs of abuse. Our increasing understanding of these epigenetic mechanisms will provide key answers to basic processes in drug addiction and hopefully provide insight into designing improved treatments for drug addiction. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:137 / 142
页数:6
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