Gorman J M
Department of Psychiatry, Columbia University, New York, NY 10032, USA.
J Clin Psychiatry. 1999;60 Suppl 17:9-13; discussion 46-8.
There is currently available evidence that suggests that drugs combining 2 synergistic mechanisms of action (e.g., enhancement of both noradrenergic and serotonergic neurotransmission) may yield superior therapeutic efficacy compared with a single therapeutic mechanism of highly selective agents such as selective serotonin reuptake inhibitors (SSRIs). The differences in antidepressant efficacy favoring dual-acting drugs may exist in particular for 3 difficult-to-treat groups of patients: those with endogenous depression, those with severe depression, or hospitalized depressed patients. Mirtazapine differs from other new dual-acting antidepressants by not being a reuptake inhibitor. Its antidepressant activity may be related to a direct enhancement of noradrenergic neurotransmission by blockade of alpha2-autoreceptors. The rapid increase in serotonin (5-HT) synaptic levels by blockade of alpha2-heteroreceptors indirectly enhances 5-HT1A-mediated neurotransmission since 5-HT2 and 5-HT3 are blocked by mirtazapine. The antidepressant efficacy of mirtazapine was established in several placebo-controlled trials. Currently available evidence suggests that mirtazapine is effective in all levels of severity of depressive illness, as well as is in a broad range of symptoms associated with depression.
目前有证据表明,与具有单一治疗机制的高选择性药物(如选择性5-羟色胺再摄取抑制剂,SSRIs)相比,联合两种协同作用机制的药物(如增强去甲肾上腺素能和5-羟色胺能神经传递)可能产生更好的治疗效果。在三类难治性患者中,尤其是内源性抑郁症患者、重度抑郁症患者或住院抑郁症患者,双作用药物在抗抑郁疗效上的差异可能尤为明显。米氮平与其他新型双作用抗抑郁药不同,它不是一种再摄取抑制剂。其抗抑郁活性可能与通过阻断α2-自身受体直接增强去甲肾上腺素能神经传递有关。通过阻断α2-异源受体,5-羟色胺(5-HT)突触水平迅速升高,间接增强了5-HT1A介导的神经传递,因为米氮平阻断了5-HT2和5-HT3。米氮平的抗抑郁疗效已在多项安慰剂对照试验中得到证实。目前的证据表明,米氮平对所有严重程度的抑郁症均有效,对与抑郁症相关的广泛症状也有效。