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

被引:13
作者
Buga, Ana Maria [1 ]
Padureanu, Vlad [2 ]
Riza, Anca-Lelia [3 ,4 ]
Oancea, Carmen Nicoleta [1 ]
Albu, Carmen Valeria [5 ]
Nica, Alexandru Dan [1 ]
机构
[1] Univ Med & Pharm Craiova, Dept Biochem, Craiova 200349, Romania
[2] Univ Med & Pharm Craiova, Dept Internal Med, Craiova 200638, Romania
[3] Univ Med & Pharm Craiova, Lab Human Genom, Craiova 200638, Romania
[4] Emergency Cty Hosp Craiova, Reg Ctr Med Genet Dolj, Craiova 200638, Romania
[5] Univ Med & Pharm Craiova, Dept Neurol, Craiova 200349, Romania
关键词
gut-brain axis; oxidative distress; neuroinflammation; inflammasomes; CENTRAL-NERVOUS-SYSTEM; OXIDATIVE STRESS; AUTOIMMUNE ENCEPHALOMYELITIS; ANIMAL-MODELS; FATTY-ACIDS; MICROBIOTA; NRF2; INFLAMMATION; ACTIVATION; QUERCETIN;
D O I
10.3390/cells12141872
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:22
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