Serotonin and depression - a riposte to Moncrieff et al. (2022).

Q3 Pharmacology, Toxicology and Pharmaceutics
Neuropsychopharmacologia Hungarica Pub Date : 2022-09-01
Zoltan Rihmer, Peter Dome, Cornelius Katona
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引用次数: 0

Abstract

In their recently published systematic "umbrella" review, Moncrieff and colleagues conclude that there is no consistent evidence that depression is caused by decreased serotonin activity in the central nervous system (CNS). However, this paper - which was extensively publicized and received a lot of attention on the social media - can cause misunderstandings, since the serotonin hypothesis of depression in its original form (i.e. reduced serotonin activity in the CNS = depression) formulated more than 50 years ago has been considered outdated for several decades. It has long been known that depression is a heterogeneous disorder not only genetically, clinically and biologically but also from a pharmacotherapeutic perspective. The decreased activity of serotonin, which undoubtedly plays an essential role in the pathogenesis of depression, is characteristic of only a subgroup of depressed subjects whose clinical picture is mostly dominated by intensified negative emotions, agitation, anxiety, insomnia, decreased appetite, self-blame and suicidality and these individuals are primarily responsive to SSRIs. By contrast, depression cases with reduced positive affects (characterized by anhedonia, anergia, inhibition and reduced cognitive functions) are mainly caused by a disturbance in the metabolism of dopamine and/or noradrenaline. These patients are primarily responsive to dual-action (e.g. SNRI) antidepressants. Results of serotonin and catecholamine (dopamine, noradrenaline) depletion studies also suggest that that the dysregulation of serotonin and dopamine/noradrenaline in the CNS is characteristic of different subgroups of depressed patients. In addition to the serotonergic, dopaminergic and noradrenergic systems, many other neurotransmitter systems (e.g. cholinergic, glutamatergic, GABAergic) and other mechanisms (e.g. neuroinfl ammation) have also been proven to play a role in the development of the disorder. Knowledge of the data presented in our publication is important since the simplistic interpretation by Moncrieffetal. of the role of serotonin in the pathogenesis of depression may undermine confidence in SSRIs in many patients. (Neuropsychopharmacol Hung 2022; 24(3): 120-125).

血清素和抑郁症——对Moncrieff等人(2022)的反驳。
在他们最近发表的系统性“保护伞”综述中,Moncrieff及其同事得出结论,没有一致的证据表明抑郁症是由中枢神经系统(CNS)中血清素活性降低引起的。然而,这篇被广泛宣传并在社交媒体上受到大量关注的论文可能会引起误解,因为50多年前提出的抑郁症的血清素假说(即中枢神经系统中血清素活性降低=抑郁症)已经过时了几十年。人们早就知道,抑郁症不仅是一种基因、临床和生物学上的异质性疾病,而且从药物治疗的角度来看也是如此。血清素活性的降低无疑在抑郁症的发病机制中起着至关重要的作用,但这只是临床表现主要为负性情绪加剧、躁动、焦虑、失眠、食欲下降、自责和自杀倾向的抑郁症患者的一个亚组的特征,这些患者主要对SSRIs有反应。相比之下,积极影响降低的抑郁症病例(以快感缺乏、无痛感、抑制和认知功能下降为特征)主要是由多巴胺和/或去甲肾上腺素代谢紊乱引起的。这些患者主要对双效抗抑郁药(如SNRI)有反应。血清素和儿茶酚胺(多巴胺、去甲肾上腺素)耗竭的研究结果也表明,中枢神经系统中血清素和多巴胺/去甲肾上腺素的失调是不同亚组抑郁症患者的特征。除了血清素能、多巴胺能和去甲肾上腺素能系统外,许多其他神经递质系统(如胆碱能、谷氨酸能、gaba能)和其他机制(如神经炎症)也被证明在该疾病的发展中起作用。由于Moncrieffetal的简单解释,我们出版物中提供的数据的知识是重要的。对血清素在抑郁症发病机制中的作用的研究可能会削弱许多患者对ssri类药物的信心。(神经精神药物,洪2022;24(3): 120 - 125)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuropsychopharmacologia Hungarica
Neuropsychopharmacologia Hungarica Medicine-Medicine (all)
CiteScore
1.60
自引率
0.00%
发文量
8
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