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药物成瘾中依赖代谢型谷氨酸受体的突触可塑性

mGluR-Dependent Synaptic Plasticity in Drug-Seeking.

作者信息

Bellone Camilla, Mameli Manuel

机构信息

Department of Basic Neuroscience, University of Geneva Geneva, Switzerland.

出版信息

Front Pharmacol. 2012 Aug 27;3:159. doi: 10.3389/fphar.2012.00159. eCollection 2012.

Abstract

A primary feature of drug addiction is the compulsive use despite negative consequences. A general consensus is emerging on the capacity of addictive substances to co-opt synaptic transmission and synaptic plasticity in brain circuits which are involved in reinforcement and reward processing. A current hypothesis is that drug-driven neuroadaptations during learning and memory processes divert the functions of these brain circuits, eventually leading to addictive behaviors. Metabotropic glutamate receptors (mGluRs) not only lead to long-term modulation of synaptic transmission but they have been implicated in drug-evoked synaptic plasticity and drug-seeking behaviors in two important ways. mGluR-dependent modulation of synaptic transmission is impaired by drug experience but interestingly their activation has been indicated as a strategy to restore baseline transmission after drug-evoked synaptic plasticity. Here we focus on the cellular mechanisms underlying mGluR-dependent long-term changes of excitatory synapses, and review results implicating these receptors in drug-evoked synaptic plasticity.

摘要

药物成瘾的一个主要特征是尽管有负面后果仍强迫性使用。关于成瘾性物质在参与强化和奖赏处理的脑回路中改变突触传递和突触可塑性的能力,正在形成一个普遍共识。当前的一个假设是,学习和记忆过程中药物驱动的神经适应性改变了这些脑回路的功能,最终导致成瘾行为。代谢型谷氨酸受体(mGluRs)不仅能导致突触传递的长期调节,而且它们在药物诱发的突触可塑性和觅药行为中以两种重要方式发挥作用。药物体验会损害mGluR依赖的突触传递调节,但有趣的是,它们的激活已被视为一种在药物诱发突触可塑性后恢复基线传递的策略。在这里,我们关注mGluR依赖的兴奋性突触长期变化的细胞机制,并综述这些受体与药物诱发突触可塑性相关的研究结果。

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