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Investigating the renoprotective effects of Polygonatum sibiricum polysaccharides (PSP) on D-galactose-induced aging mice: insights from gut microbiota and metabolomics analyses
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作者:

Huang, Rui
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h-index: 0
机构:
Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China

Che, Runli
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h-index: 0
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Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China

Sun, Taoli
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Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China

Xie, Wen
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h-index: 0
机构:
First Peoples Hosp Changde City, Changde, Peoples R China Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China

Zhang, Shuihan
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h-index: 0
机构:
Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China
机构:
[1] Hunan Univ Chinese Med, Hunan Acad Chinese Med, Changsha, Peoples R China
[2] First Peoples Hosp Changde City, Changde, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Polygonatum sibiricum polysaccharides;
renoprotection;
aging;
gut microbiota;
metabolomics;
D-ASPARTIC ACID;
D O I:
10.3389/fmicb.2025.1550971
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Introduction Polygonatum sibiricum polysaccharides (PSP) have been suggested to possess various health benefits, including anti-aging and renoprotective effects. However, the mechanisms underlying PSP's protective effects on kidney function, particularly in the context of aging, remain unclear. This study explores how PSP protects against D-galactose (D-gal)-induced kidney damage in aging mice, focusing on gut microbiota and metabolomics.Methods Mice were assigned to five groups: control, model (D-gal), vitamin C, low-dose PSP, and high-dose PSP, and treated for 8 weeks. Kidney pathology was assessed via H&E and Masson's trichrome staining. 16S rRNA sequencing analyzed gut microbiota, and non-targeted metabolomics identified metabolic changes. Correlations between gut bacteria and metabolites were examined.Results PSP alleviated renal damage, reducing tubular atrophy, epithelial swelling, and collagen deposition. It increased beneficial gut bacteria (e.g., Lactobacillus, Bifidobacterium) and altered 23 metabolites linked to pathways such as amino acid and sphingolipid metabolism. Gut microbiota and metabolites were strongly correlated, indicating PSP's role in regulating the gut-kidney axis.Conclusion PSP protects against age-related kidney damage by modulating gut microbiota and metabolic pathways, highlighting its therapeutic potential for kidney aging through the gut-kidney axis.
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