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米氮平在抑郁症临床相关亚组中的疗效。

Efficacy of mirtazapine in clinically relevant subgroups of depressed patients.

作者信息

Nutt D J

机构信息

University of Bristol, Psychopharmacology Unit, School of Medical Sciences, United Kingdom.

出版信息

Depress Anxiety. 1998;7 Suppl 1:7-10.

PMID:9597345
Abstract

Mirtazapine is a noradrenergic and specific serotonergic antidepressant (NaSSA) with a novel mode of action that differs from other antidepressants that are currently available. Clinical trials have demonstrated it to have good antidepressant efficacy and excellent tolerability. Analysis of the results of placebo-controlled trials in moderately or severely depressed patients have shown mirtazapine to be effective in clinically important subgroups of depressed patients, particularly anxious patients, patients with sleep disturbance, retarded patients, and agitated patients. The efficacy and tolerability of mirtazapine are attributable to its pharmacological profile. It is likely that the overall antidepressant activity arises from its dual action, enhancing both noradrenergic and 5-HT1 receptor-mediated serotonergic neurotransmission, while the anxiolytic and sleep-improving properties of mirtazapine are attributable to the specific blockade of 5-HT2 and 5-HT3 receptors.

摘要

米氮平是一种去甲肾上腺素能及特异性5-羟色胺能抗抑郁药(NaSSA),其作用方式新颖,与目前可用的其他抗抑郁药不同。临床试验表明它具有良好的抗抑郁疗效和出色的耐受性。对中度或重度抑郁症患者进行的安慰剂对照试验结果分析显示,米氮平在抑郁症患者的重要临床亚组中有效,尤其是焦虑患者、睡眠障碍患者、迟滞患者和激越患者。米氮平的疗效和耐受性归因于其药理特性。其整体抗抑郁活性可能源于其双重作用,即增强去甲肾上腺素能和5-HT1受体介导的5-羟色胺能神经传递,而米氮平的抗焦虑和改善睡眠特性则归因于对5-HT2和5-HT3受体的特异性阻断。

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