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The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis
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 m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378521/ https://www.ncbi.nlm.nih.gov/pubmed/37508537 http://dx.doi.org/10.3390/cells12141872 |
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author | Buga, Ana Maria Padureanu, Vlad Riza, Anca-Lelia Oancea, Carmen Nicoleta Albu, Carmen Valeria Nica, Alexandru Dan |
author_facet | Buga, Ana Maria Padureanu, Vlad Riza, Anca-Lelia Oancea, Carmen Nicoleta Albu, Carmen Valeria Nica, Alexandru Dan |
author_sort | Buga, Ana Maria |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10378521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103785212023-07-29 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 Cells Review 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. MDPI 2023-07-17 /pmc/articles/PMC10378521/ /pubmed/37508537 http://dx.doi.org/10.3390/cells12141872 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Buga, Ana Maria Padureanu, Vlad Riza, Anca-Lelia Oancea, Carmen Nicoleta Albu, Carmen Valeria Nica, Alexandru Dan The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title | The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title_full | The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title_fullStr | The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title_full_unstemmed | The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title_short | The Gut–Brain Axis as a Therapeutic Target in Multiple Sclerosis |
title_sort | gut–brain axis as a therapeutic target in multiple sclerosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378521/ https://www.ncbi.nlm.nih.gov/pubmed/37508537 http://dx.doi.org/10.3390/cells12141872 |
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