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

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

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.

Keywords: gut–brain axis; inflammasomes; neuroinflammation; oxidative distress.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain-Gut Axis
  • Gastrointestinal Microbiome*
  • Humans
  • Multiple Sclerosis* / therapy
  • Multiple Sclerosis, Chronic Progressive* / drug therapy
  • Multiple Sclerosis, Relapsing-Remitting* / drug therapy
  • Young Adult

Grants and funding

This research was funded by the University of Medicine and Pharmacy of Craiova, grant number 26/531/4/31.05.2022.