Cargando…

Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6

BACKGROUND: Metformin, a type 2 diabetes treatment, improves the cognitive function of aged mice; however, whether the protective effects of metformin on cognitive function in aged mice are associated with the gut microbiome is poorly understood. Although some studies suggest that the gut microbe co...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Xiaoqi, Shen, Junyan, Feng, Shengyu, Huang, Ce, Wang, Hao, Huo, Fengjiao, Liu, Hailiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10228018/
https://www.ncbi.nlm.nih.gov/pubmed/37254162
http://dx.doi.org/10.1186/s40168-023-01567-1
_version_ 1785050885931401216
author Zhu, Xiaoqi
Shen, Junyan
Feng, Shengyu
Huang, Ce
Wang, Hao
Huo, Fengjiao
Liu, Hailiang
author_facet Zhu, Xiaoqi
Shen, Junyan
Feng, Shengyu
Huang, Ce
Wang, Hao
Huo, Fengjiao
Liu, Hailiang
author_sort Zhu, Xiaoqi
collection PubMed
description BACKGROUND: Metformin, a type 2 diabetes treatment, improves the cognitive function of aged mice; however, whether the protective effects of metformin on cognitive function in aged mice are associated with the gut microbiome is poorly understood. Although some studies suggest that the gut microbe composition influences cognitive function and that manipulating the gut microbiota might protect against age-related cognitive dysfunction, there is no direct evidence to validate that the gut microbiota mediates the effect of metformin on cognitive improvement. RESULTS: In this study, we show that the gut microbiota is altered by metformin, which is necessary for protection against ageing-associated cognitive function declines in aged mice. Mice treated with antibiotics did not exhibit metformin-mediated cognitive function protection. Moreover, treatment with Akkermansia muciniphila, which is enriched by metformin, improved cognitive function in aged mice. Mechanistically, A. muciniphila decreased pro-inflammatory-associated pathways, particularly that of the pro-inflammatory cytokine interleukin (IL)-6, in both the peripheral blood and hippocampal profiles, which was correlated with cognitive function improvement. An IL-6 antibody protected cognitive function, and an IL-6 recombinant protein abolished the protective effect of A. muciniphila on cognitive function in aged mice. CONCLUSION: This study reveals that A. muciniphila, which is mediated in the gut microbiota by metformin, modulates inflammation-related pathways in the host and improves cognitive function in aged mice by reducing the pro-inflammatory cytokine IL-6. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01567-1.
format Online
Article
Text
id pubmed-10228018
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-102280182023-05-31 Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6 Zhu, Xiaoqi Shen, Junyan Feng, Shengyu Huang, Ce Wang, Hao Huo, Fengjiao Liu, Hailiang Microbiome Research BACKGROUND: Metformin, a type 2 diabetes treatment, improves the cognitive function of aged mice; however, whether the protective effects of metformin on cognitive function in aged mice are associated with the gut microbiome is poorly understood. Although some studies suggest that the gut microbe composition influences cognitive function and that manipulating the gut microbiota might protect against age-related cognitive dysfunction, there is no direct evidence to validate that the gut microbiota mediates the effect of metformin on cognitive improvement. RESULTS: In this study, we show that the gut microbiota is altered by metformin, which is necessary for protection against ageing-associated cognitive function declines in aged mice. Mice treated with antibiotics did not exhibit metformin-mediated cognitive function protection. Moreover, treatment with Akkermansia muciniphila, which is enriched by metformin, improved cognitive function in aged mice. Mechanistically, A. muciniphila decreased pro-inflammatory-associated pathways, particularly that of the pro-inflammatory cytokine interleukin (IL)-6, in both the peripheral blood and hippocampal profiles, which was correlated with cognitive function improvement. An IL-6 antibody protected cognitive function, and an IL-6 recombinant protein abolished the protective effect of A. muciniphila on cognitive function in aged mice. CONCLUSION: This study reveals that A. muciniphila, which is mediated in the gut microbiota by metformin, modulates inflammation-related pathways in the host and improves cognitive function in aged mice by reducing the pro-inflammatory cytokine IL-6. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01567-1. BioMed Central 2023-05-30 /pmc/articles/PMC10228018/ /pubmed/37254162 http://dx.doi.org/10.1186/s40168-023-01567-1 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Xiaoqi
Shen, Junyan
Feng, Shengyu
Huang, Ce
Wang, Hao
Huo, Fengjiao
Liu, Hailiang
Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title_full Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title_fullStr Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title_full_unstemmed Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title_short Akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
title_sort akkermansia muciniphila, which is enriched in the gut microbiota by metformin, improves cognitive function in aged mice by reducing the proinflammatory cytokine interleukin-6
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10228018/
https://www.ncbi.nlm.nih.gov/pubmed/37254162
http://dx.doi.org/10.1186/s40168-023-01567-1
work_keys_str_mv AT zhuxiaoqi akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT shenjunyan akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT fengshengyu akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT huangce akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT wanghao akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT huofengjiao akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6
AT liuhailiang akkermansiamuciniphilawhichisenrichedinthegutmicrobiotabymetforminimprovescognitivefunctioninagedmicebyreducingtheproinflammatorycytokineinterleukin6