肠道微生物群与多发性硬化症之间的联系。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-12-19 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S489454
Hua Fan, Ruile Shen, Junqiang Yan, Yongjie Bai, Qizhi Fu, Xiaofei Shi, Ganqin Du, Dongmei Wang
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引用次数: 0

摘要

这篇综述阐明了由肠道微生物群引发的焦亡在多发性硬化症(MS)发展中的关键作用,强调了其在肠-脑轴中的重要性。我们对近期文献的综合分析揭示了MS患者肠道微生物群失调(以微生物多样性减少和细菌种群变化为特征)如何深刻影响免疫调节和中枢神经系统(CNS)的完整性。焦亡是程序性细胞死亡的一种炎症形式,通过促进炎性细胞因子的释放并对中枢神经系统组织造成实质性损伤,显著加重MS。肠道微生物群通过代谢物(如短链脂肪酸和神经活性化合物)或自结构产物(如脂多糖(LPS))促进这一有害过程,脂多糖调节免疫反应并影响神经元存活。这篇综述强调了调节肠道微生物群调节焦亡的潜力,从而表明靶向这一途径可能是一种有希望的治疗策略,可以减轻多发性硬化症患者的炎症反应并保持神经元的完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyroptosis the Emerging Link Between Gut Microbiota and Multiple Sclerosis.

This review elucidates the pivotal role of pyroptosis, triggered by gut microbiota, in the development of multiple sclerosis (MS), emphasizing its significance within the gut-brain axis. Our comprehensive analysis of recent literature reveals how dysbiosis in the gut microbiota of MS patients-characterized by reduced microbial diversity and shifts in bacterial populations-profoundly impacts immune regulation and the integrity of the central nervous system (CNS). Pyroptosis, an inflammatory form of programmed cell death, significantly exacerbates MS by promoting the release of inflammatory cytokines and causing substantial damage to CNS tissues. The gut microbiota facilitates this detrimental process through metabolites such as short-chain fatty acids and neuroactive compounds, or self-structural products like lipopolysaccharides (LPS), which modulate immune responses and influence neuronal survival. This review highlights the potential of modulating gut microbiota to regulate pyroptosis, thereby suggesting that targeting this pathway could be a promising therapeutic strategy to mitigate inflammatory responses and preserve neuronal integrity in patients with MS.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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