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揭示抗抑郁药的抗炎作用:过去十年人体研究的系统综述

Unveiling the Anti-Inflammatory Effects of Antidepressants: A Systematic Review of Human Studies over the Last Decade.

作者信息

Bleibel Layla, Sokołowska Paulina, Henrykowska Gabriela, Owczarek Jacek, Wiktorowska-Owczarek Anna

机构信息

Department of Pharmacology and Toxicology, Medical University of Lodz, Żeligowskiego 7/9, 90-752 Lodz, Poland.

Department of Epidemiology and Public Health, Medical University of Lodz, Żeligowskiego 7/9, 90-752 Lodz, Poland.

出版信息

Pharmaceuticals (Basel). 2025 Jun 10;18(6):867. doi: 10.3390/ph18060867.

Abstract

: Depression ranks among the most prevalent mental health conditions globally, marked by a variety of symptoms that frequently cause significant emotional distress and impairment in individuals, alongside a high recurrence rate. The predominant approach to treating depression revolves around monoamine theory, utilizing SSRIs and SNRIs, with Esketamine emerging as a supplementary option in recent times. Nevertheless, there is a growing focus on exploring the relationship between inflammation and depression, revealing a strong correlation between the two. This insight prompts consideration of the anti-inflammatory properties of current antidepressants in their therapeutic application. : A systematic literature search was conducted using the PubMed database to identify randomized controlled trials (RCTs) and clinical trials (CTs) that assessed the in vivo anti-inflammatory effects of SSRIs (fluoxetine, escitalopram, sertraline, and paroxetine), the SNRI venlafaxine, and esketamine/ketamine in human subjects undergoing treatment for depression. The included studies were evaluated based on changes in levels of pro-inflammatory and anti-inflammatory markers in response to the antidepressant treatments. : SSRIs, SNRIs, esketamine, and ketamine (a racemic mixture of S- and R-ketamine not formally approved for the treatment of depression) exhibit anti-inflammatory effects through diverse mechanisms, such as reducing pro-inflammatory cytokines or enhancing anti-inflammatory cytokines in serum or within specific brain regions like the hippocampus and prefrontal cortex. These actions are mediated through various inflammatory pathways, including nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), the brain Nod-like receptor pyrin-containing 3 (NLRP3) inflammasome, the glutamatergic system, the gut-brain axis, the hypothalamic-pituitary axis, impaired neuroplasticity, and the kynurenine pathway. : In summary, SSRIs, SNRIs, esketamine, and ketamine exert an anti-inflammatory role alongside their antidepressant effects via these intricate mechanisms.

摘要

抑郁症是全球最普遍的心理健康问题之一,其特征是各种症状频繁导致个体严重的情绪困扰和功能损害,且复发率很高。治疗抑郁症的主要方法围绕单胺理论展开,使用选择性5-羟色胺再摄取抑制剂(SSRIs)和5-羟色胺-去甲肾上腺素再摄取抑制剂(SNRIs),艾司氯胺酮最近成为一种辅助选择。然而,人们越来越关注探索炎症与抑郁症之间的关系,结果显示二者之间存在很强的相关性。这一发现促使人们在治疗应用中考虑现有抗抑郁药的抗炎特性。

使用PubMed数据库进行了系统的文献检索,以识别评估SSRIs(氟西汀、艾司西酞普兰、舍曲林和帕罗西汀)、SNRI文拉法辛以及艾司氯胺酮/氯胺酮在接受抑郁症治疗的人类受试者体内抗炎作用的随机对照试验(RCTs)和临床试验(CTs)。纳入的研究根据抗抑郁治疗后促炎和抗炎标志物水平的变化进行评估。

SSRIs、SNRIs、艾司氯胺酮和氯胺酮(一种未正式批准用于治疗抑郁症的S-氯胺酮和R-氯胺酮的外消旋混合物)通过多种机制发挥抗炎作用,例如降低血清或海马体和前额叶皮质等特定脑区中的促炎细胞因子或增强抗炎细胞因子。这些作用是通过各种炎症途径介导的,包括活化B细胞核因子κB(NF-κB)、含pyrin结构域的Nod样受体3(NLRP3)炎性小体、谷氨酸能系统、肠-脑轴、下丘脑-垂体轴、神经可塑性受损以及犬尿氨酸途径。

总之,SSRIs、SNRIs、艾司氯胺酮和氯胺酮通过这些复杂的机制在发挥抗抑郁作用的同时还发挥抗炎作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8957/12195647/f0dfcc7179b3/pharmaceuticals-18-00867-g001.jpg

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