Institute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, Ministry of Health and National Institute on Drug Dependence, Peking University, Beijing 100191, China, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China, Center of Tianjin Mental Health, Tianjin 300222, China, and Peking-Tsinghua Center for Life Sciences and Peking University-International Data Group-McGovern Institute for Brain Research, Peking University, Beijing 100871, China.
J Neurosci. 2014 May 7;34(19):6647-58. doi: 10.1523/JNEUROSCI.5390-13.2014.
Extinction therapy has been suggested to suppress the conditioned motivational effect of drug cues to prevent relapse. However, extinction forms a new inhibiting memory rather than erasing the original memory trace and drug memories invariably return. Perineuronal nets (PNNs) are a specialized extracellular matrix around interneurons in the brain that have been suggested to be a permissive factor that allows synaptic plasticity in the adolescent brain. The degradation of PNNs caused by chondroitinase ABC (ChABC) may generate induced juvenile-like plasticity (iPlasticity) and promote experience-dependent plasticity in the adult brain. In the present study, we investigated the effect of removing PNNs in the amygdala of rat on the extinction of drug memories. We found that extinction combined with intra-amygdala injections of ChABC (0.01 U/side) prevented the subsequent priming-induced reinstatement of morphine-induced and cocaine-induced, but not food -induced, conditioned place preference (CPP). Intra-amygdala injections of ChABC alone had no effect on the retention, retrieval, or relearning of morphine-induced CPP and storage of acquired food-induced CPP. Moreover, we found that the procedure facilitated the extinction of heroin- and cocaine-seeking behavior and prevented the spontaneous recovery and drug-induced reinstatement of heroin- and cocaine-seeking behavior. We also found that the effect of PNNs degradation combined with extinction may be mediated by the potentiation of several plasticity-related proteins in the amygdala. Altogether, our findings demonstrate that a combination of extinction training with PNNs degradation in the amygdala erases drug memories and suggest that ChABC may be an attractive candidate for the prevention of relapse.
灭绝疗法被建议用于抑制药物线索的条件动机效应,以防止复发。然而,灭绝形成了一种新的抑制性记忆,而不是消除原始的记忆痕迹,药物记忆总是会恢复。周围神经毡(PNNs)是大脑中间神经元周围的一种特殊细胞外基质,被认为是允许青少年大脑突触可塑性的许可因素。软骨素酶 ABC(ChABC)引起的 PNNs 降解可能产生诱导的青少年样可塑性(iPlasticity),并促进成年大脑的经验依赖性可塑性。在本研究中,我们研究了去除大鼠杏仁核中 PNNs 对药物记忆灭绝的影响。我们发现,灭绝结合杏仁核内注射 ChABC(0.01 U/侧)可防止随后的吗啡诱导和可卡因诱导但不是食物诱导的条件位置偏好(CPP)的启动诱导复燃。单独杏仁核内注射 ChABC 对吗啡诱导 CPP 的保留、检索或重新学习以及获得性食物诱导 CPP 的存储没有影响。此外,我们发现该程序促进了海洛因和可卡因寻求行为的灭绝,并防止了海洛因和可卡因寻求行为的自发恢复和药物诱导的复燃。我们还发现,PNNs 降解与灭绝相结合的效果可能是通过增强杏仁核中的几种与可塑性相关的蛋白质来介导的。总之,我们的研究结果表明,在杏仁核中结合灭绝训练和 PNNs 降解可以消除药物记忆,并表明 ChABC 可能是预防复发的有吸引力的候选药物。