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SNRIs:作用机制和临床特征。

SNRIs: mechanism of action and clinical features.

机构信息

Neurobiology of Anxiety and Depression, Faculty of Medicine, BP 53508, 1 Rue Gaston Veil, 44035 Nantes, Ceddex 1, France.

出版信息

Expert Rev Neurother. 2002 Nov;2(6):849-58. doi: 10.1586/14737175.2.6.849.

Abstract

Specific serotonin and norepinephrine reuptake inhibitors are a relatively recent class of antidepressants which have specificities making them a therapeutic choice. They are characterized by a mixed action on both major neuroamines of depression: norepinephrine and serotonin. The double polarity of the reuptake inhibition of serotonin and norepinephrine ensures a profile of effectiveness comparable to tricyclic antidepressants and higher than selective serotonin reuptake inhibitors, especially in severe depression. The absence of affinity for muscarinic, histaminic and alpha1-adrenergic receptors and the absence of action on monoamine oxidase limits their adverse effects and allows them to be better tolerated than tricyclic antidepressants and similar to selective serotonin reuptake inhibitors. Currently, two drugs of this class are available, milnacipran and venlafaxine, but several more are in development. They are active on depressive symptoms, as well as on certain comorbid symptoms (anxiety, sleep disorders) frequently associated with depression. Serotonin and norepinephrine reuptake inhibitors allow an improved rate of response and a significant rate of remission, decreasing the risk of relapse and recurrence in the medium and long term. Due to their good tolerance, they can also be prescribed for long-term treatment and in high doses in refractory depression or with strong potential of relapse. For all these reasons, one can reasonably conclude that serotonin and norepinephrine reuptake inhibitors represent the therapeutic of choice in depression and that their prescription is likely to strongly increase in the years to come.

摘要

特异性 5-羟色胺和去甲肾上腺素再摄取抑制剂是一类相对较新的抗抑郁药,具有特定的作用机制,使其成为一种治疗选择。它们的特点是对抑郁症的两种主要神经递质:去甲肾上腺素和 5-羟色胺都具有混合作用。5-羟色胺和去甲肾上腺素再摄取抑制的双重极性确保了与三环类抗抑郁药相当且高于选择性 5-羟色胺再摄取抑制剂的疗效谱,尤其是在重度抑郁症中。对毒蕈碱、组胺和α1-肾上腺素能受体的亲和力低,以及对单胺氧化酶的作用缺失,限制了它们的不良反应,并使其比三环类抗抑郁药和类似选择性 5-羟色胺再摄取抑制剂更能耐受。目前,该类有两种药物,米那普仑和文拉法辛,但还有几种正在开发中。它们对抑郁症状以及与抑郁常相关的某些共病症状(焦虑、睡眠障碍)都有作用。5-羟色胺和去甲肾上腺素再摄取抑制剂可以提高反应率和缓解率,降低中短期复发和再发的风险。由于其良好的耐受性,它们也可以用于长期治疗和在难治性抑郁症或有强烈复发风险的情况下使用高剂量。基于所有这些原因,可以合理地得出结论,5-羟色胺和去甲肾上腺素再摄取抑制剂是抑郁症的治疗选择,其处方在未来几年可能会大幅增加。

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