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Metaplasticity at the addicted tetrapartite synapse: A common denominator of drug induced adaptations and potential treatment target for addiction

机译:上瘾的四方突触的可塑性:药物诱导适应和成瘾的潜在治疗目标的共同点

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摘要

In light of the current worldwide addiction epidemic, the need for successful therapies is more urgent than ever. Although we made substantial progress in our basic understanding of addiction, reliable therapies are lacking. Since 40-60% of patients treated for substance use disorder return to active substance use within a year following treatment discharge, alleviating the vulnerability to relapse is regarded as the most promising avenue for addiction therapy. Preclinical addiction research often focuses on maladaptive synaptic plasticity within the reward pathway. However, drug induced neuroadaptations do not only lead to a strengthening of distinct drug associated cues and operant behaviors, but also seem to increase plasticity thresholds for environmental stimuli that are not associated with the drug. This form of higher order plasticity, or synaptic metaplasticity, is not expressed as a change in the efficacy of synaptic transmission but as a change in the direction or degree of plasticity induced by a distinct stimulation pattern. Experimental addiction research has demonstrated metaplasticity after exposure to multiple classes of addictive drugs. In this review we will focus on the concept of synaptic metaplasticity in the context of preclinical addiction research. We will take a closer look at the tetrapartite glutamatergic synapse and outline forms of metaplasticity that have been described at the addicted synapse. Finally we will discuss the different potential avenues for pharmacotherapies that target glutamatergic synaptic plasticity and metaplasticity. Here we will argue that aberrant metaplasticity renders the reward seeking circuitry more rigid and hence less able to adapt to changing environmental contingencies. An understanding of the molecular mechanisms that underlie this metaplasticity is crucial for the development of new strategies for addiction therapy. The correction of drug-induced metaplasticity could be used to support behavioral and pharmacotherapies for the treatment of addiction.
机译:鉴于当前全球成瘾流行,成功治疗的需求比以往任何时候都更为紧迫。尽管我们在对成瘾的基本理解上取得了实质性进展,但仍缺乏可靠的疗法。由于接受药物滥用治疗的患者中有40-60%在出院后一年内恢复活性物质使用,因此缓解复发易感性被认为是成瘾疗法的最有希望的途径。临床前成瘾研究通常集中于奖励途径内的适应不良的突触可塑性。但是,药物诱导的神经适应不仅导致与药物相关的独特线索和操作行为的增强,而且似乎增加了与药物无关的环境刺激的可塑性阈值。这种高阶可塑性或突触可塑性的形式,并不表示为突触传递功效的变化,而是表示为不同刺激模式引起的可塑性方向或程度的变化。实验性成瘾研究表明,暴露于多种成瘾药物后可发生可塑性。在这篇综述中,我们将集中在临床前成瘾研究的背景下突触可塑性的概念。我们将仔细研究成瘾突触中描述的四部分谷氨酸能突触和化生形式的轮廓。最后,我们将讨论针对谷氨酸能突触可塑性和化生可塑性的药物治疗的不同潜在途径。在这里,我们将论证异常的可塑性会导致寻求奖励的电路更加僵化,因此无法适应不断变化的环境突发事件。对形成这种可塑性的分子机制的理解对于成瘾疗法新策略的发展至关重要。药物诱导的可塑性的校正可用于支持行为和药物疗法来治疗成瘾。

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