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Cholestyramine alleviates bone and muscle loss in irritable bowel syndrome via regulating bile acid metabolism.

Ming ChenWei WeiYi LiSiliang GeJunmin ShenJiayu GuoYu ZhangXiang HuangXinyu SunDongliang ChengHuayong ZhengFeifan ChangJunyu ChenJiang LiuQinxiang ZhangTianjunke ZhouKang YuPei-Fu Tang
Published in: Cell proliferation (2024)
Irritable bowel syndrome (IBS) is a widespread gastrointestinal disorder known for its multifaceted pathogenesis and varied extraintestinal manifestations, yet its implications for bone and muscle health are underexplored. Recent studies suggest a link between IBS and musculoskeletal disorders, but a comprehensive understanding remains elusive, especially concerning the role of bile acids (BAs) in this context. This study aimed to elucidate the potential contribution of IBS to bone and muscle deterioration via alterations in gut microbiota and BA profiles, hypothesizing that cholestyramine could counteract these adverse effects. We employed a mouse model to characterize IBS and analysed its impact on bone and muscle health. Our results revealed that IBS promotes bone and muscle loss, accompanied by microbial dysbiosis and elevated BAs. Administering cholestyramine significantly mitigated these effects, highlighting its therapeutic potential. This research not only confirms the critical role of BAs and gut microbiota in IBS-associated bone and muscle loss but also demonstrates the efficacy of cholestyramine in ameliorating these conditions, thereby contributing significantly to the field's understanding and offering a promising avenue for treatment.
Keyphrases
  • irritable bowel syndrome
  • bone mineral density
  • skeletal muscle
  • soft tissue
  • mouse model
  • bone loss
  • healthcare
  • bone regeneration
  • human health
  • health information
  • risk assessment
  • combination therapy