Lactiplantibacillus plantarum CCFM8661 alleviates D-galactose-induced brain aging in mice by the regulation of the gut microbiota

Aging is characterized by a decline in biological functions, leading to various health issues. There is significant interest in mitigating age and age-related health issues. Gut microbiota has emerged as a crucial target for combating aging and influencing host health. This study evaluated the anti-...

Full description

Saved in:
Bibliographic Details
Published inFood & function Vol. 14; no. 22; pp. 10135 - 10150
Main Authors Chen, Feng, Pan, Jiani, Yu, Leilei, Wang, Shunhe, Zhang, Chengcheng, Zhao, Jianxin, Narbad, Arjan, Zhai, Qixiao, Tian, Fengwei
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 13.11.2023
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Aging is characterized by a decline in biological functions, leading to various health issues. There is significant interest in mitigating age and age-related health issues. Gut microbiota has emerged as a crucial target for combating aging and influencing host health. This study evaluated the anti-aging effects of CCFM8661 in mice and the role of the gut microbiota in mediating its effects. Aging was induced in mice using D-galactose, and CCFM8661 was orally administered for 8 weeks to evaluate its effects on age-related decline and the gut microbiota. The results demonstrated that supplementation with CCFM8661 effectively alleviated cognitive impairment and oxidative stress in the aging brain, as well as liver oxidation and bone damage, and impaired intestinal barrier function in aging mice. Furthermore, CCFM8661 modulated the gut microbiota of aging mice, increasing the abundance of beneficial bacteria, such as Ruminococcaceae, and influenced the functionality of the gut microbiota to promote the production of active metabolites. These findings suggest that CCFM8661 has a mitigating effect on organismal aging, especially brain aging.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2042-6496
2042-650X
DOI:10.1039/d3fo03377e