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首页> 外文期刊>Neurobiology of learning and memory >Metaplasticity at the addicted tetrapartite synapse: A common denominator of drug induced adaptations and potential treatment target for addiction
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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:上瘾的四氨酸突触的血管塑性:药物诱导适应和潜在治疗靶标的常见分母

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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 drug conditioned 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:鉴于目前的全球成瘾流行病,对成功疗法的需求比以往任何时候都更加紧迫。虽然我们在我们对成瘾的基本理解方面取得了实质性进展,但缺乏可靠的疗法。由于40-60%的物质使用障碍治疗的患者在治疗放弃后一年内恢复活性物质,缓解复发的脆弱性被认为是最有前途的成瘾治疗途径。临床前成瘾研究往往侧重于奖励途径内的适应性突触可塑性。然而,药物诱导的神经展开不仅导致强化不同的药物相关的提示和药物条件行为,而且似乎增加了与药物无关的环境刺激的可塑性阈值。这种高阶塑性或突触型塑料形成的形式不会表示为突触传递的功效的变化,而是作为由不同刺激模式引起的塑性方向或程度的变化。实验性瘾研究在暴露于多种患者的上瘾药物后表现出了术前性。在这篇综述中,我们将专注于临床前成瘾研究中突触荟萃塑化的概念。我们将仔细看看,在上瘾的Synapse中描述的四颗粒谷氨酸突触突触和概述的概要形式。最后,我们将讨论靶向谷氨酸突触突触塑性和沟塑性的药物治疗的不同潜在途径。在这里,我们将争辩说,异常的荟萃塑化使得奖励寻求电路更加僵硬,因此不太能够适应改变环境突发事件。理解利于这种多相性的分子机制对于开发成瘾治疗的新策略至关重要。药物诱导的沟塑性的校正可用于支持对成瘾治疗的行为和药物治疗。

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