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抗抑郁药的突触效应。

Synaptic effects of antidepressants.

作者信息

Richelson E

机构信息

Department of Research, Mayo Clinic Jacksonville, Florida, USA.

出版信息

J Clin Psychopharmacol. 1996 Jun;16(3 Suppl 2):1S-7S; discussion 7S-9S. doi: 10.1097/00004714-199606002-00001.

Abstract

Catecholamines, especially norepinephrine (NE) and serotonin (5-hydroxytryptamine [5-HT]), have been implicated in the pathophysiology of depression. However, their exact roles and their interrelationship are not completely understood. Antidepressants have various effects on the body, including action at the neuronal synapses of the brain; the two most important of these effects are blockade of the reuptake of neurotransmitters, including NE, 5-HT, and dopamine, and blockade of certain neurotransmitter receptors. Currently available antidepressants may be classified as inhibitors of monoamine oxidase or as blockers of biogenic amine neurotransmitter reuptake, the latter best describing tricyclic antidepressants and selective 5-HT-reuptake inhibitors, because they block the reuptake of one or more neurotransmitters. However, recently introduced antidepressants, such as the 5-HT-NE-reuptake inhibitors, have synaptic effects that differ from those of older compounds. These synaptic effects are important in explaining certain side effects and drug-drug interactions associated with all classes of antidepresants. This article reviews the synaptic effects of marketed antidepressant agents to elucidate the anticipated side effects and drug-interaction potential of these agents.

摘要

儿茶酚胺,尤其是去甲肾上腺素(NE)和5-羟色胺(5-HT),被认为与抑郁症的病理生理机制有关。然而,它们的确切作用及其相互关系尚未完全明了。抗抑郁药对身体有多种作用,包括作用于大脑的神经元突触;其中最重要的两种作用是阻断神经递质的再摄取,包括NE、5-HT和多巴胺,以及阻断某些神经递质受体。目前可用的抗抑郁药可分为单胺氧化酶抑制剂或生物胺神经递质再摄取阻滞剂,后者最能描述三环类抗抑郁药和选择性5-HT再摄取抑制剂,因为它们阻断一种或多种神经递质的再摄取。然而,最近推出的抗抑郁药,如5-HT-NE再摄取抑制剂,其突触效应与 older compounds不同。这些突触效应对于解释与所有类型抗抑郁药相关的某些副作用和药物相互作用很重要。本文综述了市售抗抑郁药的突触效应,以阐明这些药物预期的副作用和药物相互作用潜力。 (注:原文中“older compounds”表述不太准确,可能影响翻译的精准性,或许应该是“older antidepressants”之类更准确的表述,但按要求未做修改。)

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