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精神分裂症的药物治疗:抗精神病药物蓄积、治疗作用及失效的机制

Pharmacotherapy of schizophrenia: Mechanisms of antipsychotic accumulation, therapeutic action and failure.

作者信息

Chestnykh Daria A, Amato Davide, Kornhuber Johannes, Müller Christian P

机构信息

Department of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University Erlangen-Nuremberg, Schwabachanlage 6, 91054, Erlangen, Germany.

Department of Psychiatry and Psychotherapy, University Clinic, Friedrich-Alexander-University Erlangen-Nuremberg, Schwabachanlage 6, 91054, Erlangen, Germany; Department of Neuroscience, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Behav Brain Res. 2021 Apr 9;403:113144. doi: 10.1016/j.bbr.2021.113144. Epub 2021 Jan 27.

Abstract

Schizophrenia is a multi-dimensional disorder with a complex and mostly unknown etiology, leading to a severe decline in life quality. Antipsychotic drugs (APDs) remain beneficial interventions in the treatment of the disorder, but vary significantly in binding profile, clinical effects and adverse reactions. The present review summarizes the main principles of APD mechanisms of action with a particular focus on recent findings in APD accumulation and its role in the therapeutic efficacy and treatment failure. High and low doses of APDs were shown to be effective in different dimensions of antipsychotic-like behaviour in rodent models. Efficacy of the APDs correlates with high dopamine D2 receptor occupancy, which occurs quickly after drug administration. However, onset and peak of action are delayed up to several days or weeks. APD accumulation via acidic trapping in synaptic vesicles is considered to underlie the time course of APD action. Use-dependent exocytosis, co-release with dopamine and serotonin and inhibition of ion channels impact on the neuronal transmission and determine effects of APDs. Disruption in accumulating properties leads to diminished APD effects. In addition, long-term APD administration at therapeutic doses leads to treatment failure both in animal models and in humans. APD failure was associated with treatment induced neuroadaptations, including a decline in extracellular dopamine levels, dopamine transporter upregulation, and altered neuronal firing. However, enhanced synaptic vesicle release has also been reported. APD loss of efficacy may be reversed through inhibition of the dopamine transporter or switching the administration regimen from continuous to intermittent. Thus, manipulating the accumulation properties of APDs, changes in the administration regimen and doses, or co-administration with dopamine transporter inhibitors may be considered to yield benefits in the development of new effective strategies in the treatment of schizophrenia.

摘要

精神分裂症是一种多维度的疾病,病因复杂且大多未知,会导致生活质量严重下降。抗精神病药物(APD)仍然是治疗该疾病的有益干预措施,但在结合特性、临床效果和不良反应方面差异很大。本综述总结了APD作用机制的主要原理,特别关注APD蓄积的最新研究结果及其在治疗效果和治疗失败中的作用。在啮齿动物模型中,高剂量和低剂量的APD在抗精神病样行为的不同维度上均显示出有效性。APD的疗效与高多巴胺D2受体占有率相关,给药后很快就会出现这种情况。然而,起效和作用峰值会延迟数天或数周。通过酸性捕获在突触小泡中蓄积APD被认为是APD作用时间过程的基础。依赖使用的胞吐作用、与多巴胺和5-羟色胺的共同释放以及对离子通道的抑制会影响神经元传递并决定APD的作用。蓄积特性的破坏会导致APD效果减弱。此外,在动物模型和人类中,以治疗剂量长期服用APD都会导致治疗失败。APD治疗失败与治疗引起的神经适应性变化有关,包括细胞外多巴胺水平下降、多巴胺转运体上调以及神经元放电改变。然而,也有报道称突触小泡释放增强。通过抑制多巴胺转运体或将给药方案从持续给药改为间歇给药,可能会逆转APD疗效丧失的情况。因此,在开发治疗精神分裂症的新有效策略时,可以考虑操纵APD的蓄积特性、改变给药方案和剂量,或与多巴胺转运体抑制剂联合使用,以产生有益效果。

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