Gillman P Ken
Pioneer Valley Private Hospital, Australia.
Hum Psychopharmacol. 2006 Mar;21(2):117-25. doi: 10.1002/hup.750.
A systematic review of published work concerning mirtazapine was undertaken to assess possible evidence of serotonergic effects or serotonin toxicity (ST) in humans, because drug toxicity and interaction data from human over-doses is an useful source of information about the nature and potency of drug effects. There is a paucity of evidence for mirtazapine having effects on any indicator of serotonin elevation, which leads to an emphasis on ST as an important line of evidence. Mirtazapine is compared with its analogue mianserin, and other serotonergic drugs. Although mirtazapine is referred to as a dual-action 'noradrenergic and specific serotonergic drug' (NaSSA) little evidence to support that idea exists, except from initial microdialysis studies in animals showing small effects; those have not subsequently been replicated or substantiated by independent researchers. Also, new data indicate its affinity for Alpha 2 adrenoceptors is not different to mianserin. It appears to exhibit no serotonergic symptoms or toxicity in over-dose by itself, nor is there evidence that it precipitates ST in combination with monoamine oxidase inhibitors, as would be expected if it raises intra-synaptic serotonin levels. Mirtazapine has no demonstrable serotonergic effects in humans and there is insufficient evidence to designate it as a dual-action drug.
对已发表的有关米氮平的研究进行了系统综述,以评估其在人体中产生血清素能效应或血清素毒性(ST)的可能证据,因为来自人类过量用药的药物毒性和相互作用数据是了解药物效应性质和强度的有用信息来源。几乎没有证据表明米氮平对血清素升高的任何指标有影响,这使得ST成为一条重要的证据线。将米氮平与其类似物米安色林以及其他血清素能药物进行了比较。尽管米氮平被称为“去甲肾上腺素能和特异性血清素能双重作用药物”(NaSSA),但除了最初在动物身上进行的微透析研究显示有微小作用外,几乎没有证据支持这一观点;这些研究后来没有被独立研究人员重复或证实。此外,新数据表明它对α2肾上腺素能受体的亲和力与米安色林并无差异。它本身过量用药时似乎不会出现血清素能症状或毒性,也没有证据表明它与单胺氧化酶抑制剂合用时会引发ST,而如果它会提高突触内血清素水平,情况就会是这样。米氮平在人体中没有可证实的血清素能效应,且没有足够证据将其指定为双重作用药物。