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精神药物所致体重增加:机制与管理

Psychotropic drug induced weight gain: mechanisms and management.

作者信息

Bernstein J G

机构信息

Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge 02142.

出版信息

Clin Neuropharmacol. 1988;11 Suppl 1:S194-206.

PMID:3052818
Abstract

Most of the drugs commonly used in the treatment and prophylaxis of depression, mania, and psychotic illness have, as one of their prominent side effects, the ability to increase appetite, stimulate carbohydrate craving, and promote weight gain. These side effects are troublesome to patients, and frequently constitute a major reason for premature discontinuation of therapy. This review examines the relative likelihood of the occurrence of appetite stimulation and weight gain with various psychotropic medications. Potential mechanisms of these effects and strategies to minimize or avoid weight gain during pharmacotherapy of psychiatric illness are examined. Evidence suggests that those compounds, which either antagonize or downregulate serotonin receptors, are more likely to stimulate carbohydrate hunger and weight gain. Amitriptyline, chlorpromazine, mesoridazine, thioridazine, and lithium are most likely to produce weight gain. Compounds that have more pronounced serotonergic action, such as fluoxetine and fenfluramine, are more likely to decrease carbohydrate craving and promote weight loss.

摘要

大多数常用于治疗和预防抑郁症、躁狂症及精神病性疾病的药物,其突出副作用之一是能够增加食欲、激发对碳水化合物的渴望并促进体重增加。这些副作用给患者带来困扰,且常常成为治疗过早中断的主要原因。本综述探讨了各种精神药物引发食欲刺激和体重增加的相对可能性。研究了这些效应的潜在机制以及在精神疾病药物治疗期间尽量减少或避免体重增加的策略。有证据表明,那些拮抗或下调血清素受体的化合物更有可能激发对碳水化合物的渴望和导致体重增加。阿米替林、氯丙嗪、美索达嗪、硫利达嗪和锂最有可能导致体重增加。具有更显著血清素能作用的化合物,如氟西汀和芬氟拉明,则更有可能减少对碳水化合物的渴望并促进体重减轻。

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