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The Gut-Brain Axis as a Therapeutic Target in Multiple Sclerosis.
Buga, Ana Maria; Padureanu, Vlad; Riza, Anca-Lelia; Oancea, Carmen Nicoleta; Albu, Carmen Valeria; Nica, Alexandru Dan.
Afiliação
  • Buga AM; Department of Biochemistry, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Padureanu V; Department of Internal Medicine, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
  • Riza AL; Laboratory of Human Genomics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
  • Oancea CN; Regional Center for Medical Genetics Dolj, Emergency County Hospital Craiova, 200638 Craiova, Romania.
  • Albu CV; Department of Biochemistry, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Nica AD; Department of Neurology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Cells ; 12(14)2023 07 17.
Article em En | MEDLINE | ID: mdl-37508537
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Crônica Progressiva / Esclerose Múltipla Recidivante-Remitente / Microbioma Gastrointestinal / Esclerose Múltipla Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Crônica Progressiva / Esclerose Múltipla Recidivante-Remitente / Microbioma Gastrointestinal / Esclerose Múltipla Idioma: En Ano de publicação: 2023 Tipo de documento: Article