Biological and therapeutic significance of targeting NLRP3 inflammasome in the brain and the current efforts to develop brain-penetrant inhibitors.

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in pharmacology Pub Date : 2025-01-01 Epub Date: 2024-11-08 DOI:10.1016/bs.apha.2024.10.004
Baljit Kaur, Savannah Biby, Jannatun N Namme, Sayaji More, Yiming Xu, Shijun Zhang
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引用次数: 0

Abstract

NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome, a pivotal regulator of the innate immune system, orchestrates inflammatory responses implicated in neurodegenerative and inflammatory diseases. Over the past 20 years, the exploration of NLRP3 activation pathways has advanced significantly. Upon NLRP3 activation, it initiates the formation of a cytosolic multiprotein complex known as the inflammasome. This complex activates caspase-1, which then processes proinflammatory cytokines IL-1β and IL-18 and leads to gasdermin-mediated cell death, pyroptosis. Structural insights into NLRP3 inflammasome assembly and caspase-1 activation have spurred development of novel small molecule inhibitors targeting this pathway, aiming to mitigate excessive inflammation without compromising immune surveillance. The initial NLRP3 inhibitor reported was glyburide, an FDA-approved antidiabetic drug of the sulfonylurea class, which was found to inhibit the release of IL-1β induced by stimuli in human monocytes and murine macrophages. Subsequently, MCC950 (also known as CRID3), a direct NLRP3 inhibitor, was discovered. While showing promising results in preclinical and clinical trials for treating diseases, higher doses of MCC950 led to elevated transaminase levels and hepatotoxicity concerns. Recent studies using MCC950 as a research tool have prompted the development of safer and more effective NLRP3 inhibitors, including a series of compounds currently undergoing clinical trials, highlighting the potential of NLRP3 inhibitors in attenuating disease progression and improving therapeutic outcomes. In this chapter, we delve into the latest progress in understanding the mechanism of NLRP3 inflammasome activation and its roles in the pathophysiology of neurological diseases. We also summarize recent development of small molecule NLRP3 inhibitors along with the associated obstacles and concerns.

靶向NLRP3炎性体在脑中的生物学和治疗意义以及目前开发脑渗透抑制剂的努力。
nod样受体家族pyrin结构域含有3 (NLRP3)炎性小体,是先天免疫系统的关键调节因子,协调涉及神经退行性和炎症性疾病的炎症反应。在过去的20年里,对NLRP3激活途径的探索取得了显著进展。当NLRP3被激活时,它启动了称为炎性体的细胞质多蛋白复合物的形成。该复合物激活caspase-1, caspase-1随后加工促炎细胞因子IL-1β和IL-18,并导致气真皮蛋白介导的细胞死亡,即焦亡。对NLRP3炎症小体组装和caspase-1激活的结构洞察刺激了针对该途径的新型小分子抑制剂的开发,旨在减轻过度炎症而不影响免疫监视。最初报道的NLRP3抑制剂是格列本脲,一种fda批准的磺脲类降糖药物,被发现可以抑制刺激诱导的人单核细胞和小鼠巨噬细胞IL-1β的释放。随后,发现了一种直接的NLRP3抑制剂MCC950(也称为CRID3)。虽然在治疗疾病的临床前和临床试验中显示出令人鼓舞的结果,但高剂量的MCC950会导致转氨酶水平升高和肝毒性问题。最近使用MCC950作为研究工具的研究促进了更安全、更有效的NLRP3抑制剂的开发,包括一系列正在进行临床试验的化合物,突出了NLRP3抑制剂在减缓疾病进展和改善治疗结果方面的潜力。在本章中,我们将深入探讨NLRP3炎性体激活机制及其在神经系统疾病病理生理中的作用的最新进展。我们还总结了小分子NLRP3抑制剂的最新发展以及相关的障碍和问题。
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
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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