将炎症小体复合物作为治疗情绪障碍的新策略。

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY Expert Opinion on Therapeutic Targets Pub Date : 2024-05-01 Epub Date: 2024-06-18 DOI:10.1080/14728222.2024.2366872
Aline Silva de Miranda, Eliana Cristina de Brito Toscano, Jason C O'Connor, Antonio Lucio Teixeira
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引用次数: 0

摘要

导言:炎症小体复合物,尤其是NLRP3,作为情绪障碍的潜在治疗靶点,已引起人们的极大关注。NLRP3 触发依赖于caspase 1的炎性细胞因子IL-1β和IL-18的释放,并似乎与嘌呤能和犬尿氨酸通路相互作用,而所有这些通路都与情绪障碍的发生和发展有关:新出现的证据支持 NLRP3 炎症小体成为治疗情绪障碍的药物靶点。我们讨论了来自动物模型和人体研究的现有证据,并对这一新靶点的缺点和前景进行了反思:多项研究支持 NLRP3 炎症小体参与 MDD。然而,大多数证据来自动物模型。NLRP3 炎症小体在 BD 中的作用及其抗躁狂特性尚不十分明确,需要进一步探索。有证据表明,P2×R7拮抗剂具有抗躁狂作用,在小鼠躁狂症模型中与降低脑内IL-1β和TNF-α水平有关。除小胶质细胞外,其他表达 NLRP3 炎症小体的细胞(如星形胶质细胞)以及其他炎症小体复合物参与情绪失调的情况也值得进一步研究。在考虑包括临床试验在内的转化方法之前,需要对情绪失调症中的 NLRP3 和其他炎性体进行临床前和临床表征。
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Targeting inflammasome complexes as a novel therapeutic strategy for mood disorders.

Introduction: Inflammasome complexes, especially NLRP3, have gained great attention as a potential therapeutic target in mood disorders. NLRP3 triggers a caspase 1-dependent release of the inflammatory cytokines IL-1β and IL-18, and seems to interact with purinergic and kynurenine pathways, all of which are implicated in mood disorders development and progression.

Areas covered: Emerging evidence supports NLRP3 inflammasome as a promising pharmacological target for mood disorders. We discussed the available evidence from animal models and human studies and provided a reflection on drawbacks and perspectives for this novel target.

Expert opinion: Several studies have supported the involvement of NLRP3 inflammasome in MDD. However, most of the evidence comes from animal models. The role of NLRP3 inflammasome in BD as well as its anti-manic properties is not very clear and requires further exploration. There is evidence of anti-manic effects of P2×R7 antagonists associated with reduction in the brain levels of IL-1β and TNF-α in a murine model of mania. The involvement of other NLRP3 inflammasome expressing cells besides microglia, like astrocytes, and of other inflammasome complexes in mood disorders also deserves further investigation. Preclinical and clinical characterization of NLRP3 and other inflammasomes in mood disorders is needed before considering translational approaches, including clinical trials.

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来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
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