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Epimedii Folium decoction ameliorates osteoporosis in mice through NLRP3/caspase-1/IL-1β signalling pathway and gut-bone axis.
- Source :
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International immunopharmacology [Int Immunopharmacol] 2024 Aug 20; Vol. 137, pp. 112472. Date of Electronic Publication: 2024 Jun 18. - Publication Year :
- 2024
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Abstract
- Aim of the Study: This study aimed to determine the effect of Epimedium brevicornu Maxim. (EF) on osteoporosis (OP) and its underlying molecular mechanisms, and to explore the existence of the "Gut-Bone Axis".<br />Material and Methods: The impact of EF decoction (EFD) on OP was evaluated using istopathological examination and biochemical assays. Targeted metabolomics was employed to identify key molecules and explore their molecular mechanisms. Alterations in the gut microbiota (GM) were evaluated by 16S rRNA gene sequencing. The role of the GM was clarified using an antibiotic cocktail and faecal microbiota transplantation.<br />Results: EFD significantly increased the weight (14.06%), femur length (4.34%), abdominal fat weight (61.14%), uterine weight (69.86%), and insulin-like growth factor 1 (IGF-1) levels (59.48%), while reducing serum type I collagen cross-linked carboxy-terminal peptide (CTX-I) levels (15.02%) in osteoporotic mice. The mechanism of action may involve the regulation of the NLRP3/cleaved caspase-1/IL-1β signalling pathway in improving intestinal tight junction proteins and bone metabolism. Additionally, EFD modulated the abundance of related GM communities, such as Lactobacillus, Coriobacteriaceae, bacteria of family S24-7, Clostridiales, and Prevotella, and increased propionate and butyrate levels. Antibiotic-induced dysbiosis of gut bacteria disrupted OP regulation of bone metabolism, which was restored by the recovery of GM.<br />Conclusions: Our study is the first to demonstrate that EFD works in an OP mouse model by utilising GM and butyric acid. Thus, EF shows promise as a potential remedy for OP in the future.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024. Published by Elsevier B.V.)
- Subjects :
- Animals
Mice
Female
Disease Models, Animal
Mice, Inbred C57BL
Bone and Bones drug effects
Bone and Bones metabolism
Insulin-Like Growth Factor I metabolism
Fecal Microbiota Transplantation
NLR Family, Pyrin Domain-Containing 3 Protein metabolism
Gastrointestinal Microbiome drug effects
Osteoporosis drug therapy
Osteoporosis metabolism
Signal Transduction drug effects
Caspase 1 metabolism
Interleukin-1beta metabolism
Epimedium
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1705
- Volume :
- 137
- Database :
- MEDLINE
- Journal :
- International immunopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 38897131
- Full Text :
- https://doi.org/10.1016/j.intimp.2024.112472