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肠脑轴作为多发性硬化症的治疗靶点。

The Gut-Brain Axis as a Therapeutic Target in Multiple Sclerosis.

机构信息

Department of Biochemistry, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.

Department of Internal Medicine, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.

出版信息

Cells. 2023 Jul 17;12(14):1872. doi: 10.3390/cells12141872.

DOI:10.3390/cells12141872
PMID:37508537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10378521/
Abstract

The CNS is very susceptible to oxidative stress; the gut microbiota plays an important role as a trigger of oxidative damage that promotes mitochondrial dysfunction, neuroinflammation, and neurodegeneration. In the current review, we discuss recent findings on oxidative-stress-related inflammation mediated by the gut-brain axis in multiple sclerosis (MS). Growing evidence suggests targeting gut microbiota can be a promising strategy for MS management. Intricate interaction between multiple factors leads to increased intra- and inter-individual heterogeneity, frequently painting a different picture in vivo from that obtained under controlled conditions. Following an evidence-based approach, all proposed interventions should be validated in clinical trials with cohorts large enough to reach significance. Our review summarizes existing clinical trials focused on identifying suitable interventions, the suitable combinations, and appropriate timings to target microbiota-related oxidative stress. Most studies assessed relapsing-remitting MS (RRMS); only a few studies with very limited cohorts were carried out in other MS stages (e.g., secondary progressive MS-SPMS). Future trials must consider an extended time frame, perhaps starting with the perinatal period and lasting until the young adult period, aiming to capture as many complex intersystem interactions as possible.

摘要

中枢神经系统(CNS)非常容易受到氧化应激的影响;肠道微生物群作为氧化损伤的触发因素,在促进线粒体功能障碍、神经炎症和神经退行性变方面发挥着重要作用。在本综述中,我们讨论了与肠道-大脑轴相关的氧化应激相关炎症在多发性硬化症(MS)中的最新发现。越来越多的证据表明,靶向肠道微生物群可能是 MS 管理的一种有前途的策略。多种因素之间的复杂相互作用导致个体内和个体间的异质性增加,这经常导致体内情况与受控条件下获得的情况不同。我们的综述总结了现有的临床试验,这些试验集中于确定合适的干预措施、合适的组合以及适当的时机来靶向与微生物群相关的氧化应激。大多数研究评估了复发缓解型多发性硬化症(RRMS);只有少数在其他 MS 阶段(例如继发性进展型多发性硬化症-SPMS)进行的研究具有非常有限的队列。未来的试验必须考虑更广泛的时间框架,也许从围产期开始,持续到青年期,以尽可能多地捕捉到复杂的系统间相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c12/10378521/7663f6b8e1db/cells-12-01872-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c12/10378521/8c2b0d1c4872/cells-12-01872-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c12/10378521/7663f6b8e1db/cells-12-01872-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c12/10378521/8c2b0d1c4872/cells-12-01872-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c12/10378521/7663f6b8e1db/cells-12-01872-g002.jpg

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