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曲唑酮相关口下颌运动障碍的假定作用机制。

Putative Mechanism of Action of Trazodone-Related Oromandibular Dyskinesia.

作者信息

Schneider Alan L

机构信息

University of Southern California Keck School of Medicine, Los Angeles, CA, USA.

出版信息

Case Rep Psychiatry. 2024 Mar 31;2024:5543023. doi: 10.1155/2024/5543023. eCollection 2024.

Abstract

This is a case report of three cases of trazodone-induced buccal-lingual dyskinesias. Each case demonstrated the distinct pattern of the development of this dyskinesia after trazodone exposure for several months. All cases showed abrupt cessation of the movement disorder when the drug was discontinued. One of the three cases demonstrated a highly unusual presentation of an on/off pattern of buccal dyskinesia directly related to repetitive exposure and termination of the drug trazodone. Two of the three cases had no prior exposure to any dopamine blocking agents. One of the three had a distant exposure to a dopamine antagonist. As opposed to other antidepressants, trazodone has a mechanism of action which can account for both the development and treatment of dyskinetic movements. Its metabolite, M/chlorophenylpiperazine (M-CPP) is a 5HT2C agonist capable of causing abnormal oral-facial movements in rodent models. The presence of oromandibular dyskinetic movements can occur spontaneously with age, with trazodone being a potential predisposing factor. This article will discuss proposed mechanisms for trazodone's action with an emphasis on case reports of dystonic movements.

摘要

这是一篇关于三例曲唑酮诱发颊舌运动障碍的病例报告。每例均展示了曲唑酮暴露数月后这种运动障碍发展的独特模式。所有病例在停药后运动障碍均突然停止。三例中的一例表现出一种极为罕见的颊部运动障碍开/关模式,这与曲唑酮的反复暴露和停药直接相关。三例中有两例此前未接触过任何多巴胺阻断剂。三例中有一例曾远距离接触过一种多巴胺拮抗剂。与其他抗抑郁药不同,曲唑酮的作用机制既能解释运动障碍的发生,也能解释其治疗。其代谢产物M/氯苯基哌嗪(M - CPP)是一种5HT2C激动剂,在啮齿动物模型中能够引起异常的口面部运动。口下颌运动障碍可随年龄自然发生,曲唑酮是一个潜在的诱发因素。本文将讨论曲唑酮作用的推测机制,重点是张力障碍性运动的病例报告。

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