Alisol B 23-Acetate Ameliorates Azoxymethane/Dextran Sodium Sulfate-Induced Male Murine Colitis-Associated Colorectal

Huai-Chang Zhu1,2, Xiao-Kang Jia1,2,3, Yong Fan1,2

  • 1College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

Insights

Alisol B 23-acetate (AB23A), a natural compound, shows promise in preventing colitis-associated cancer (CAC). It alleviates disease symptoms and modulates gut microbiota, offering potential therapeutic benefits for CAC.

Area of Science:

  • Gastroenterology and Oncology
  • Natural Product Chemistry
  • Microbiome Research

Background:

  • Colitis-associated cancer (CAC) prevention and treatment are actively researched, with a focus on natural compounds modulating intestinal flora.
  • Alisol B 23-acetate (AB23A), a triterpenoid from Alismatis rhizoma, is traditionally used for gastrointestinal ailments.

Purpose of the Study:

  • To investigate the potential of AB23A in preventing azoxymethane (AOM) and dextran sulfate sodium (DSS)-induced CAC in male mice.
  • To elucidate the molecular mechanisms and gut microbiota changes associated with AB23A intervention in CAC models.

Main Methods:

  • Induction of CAC in male mice using AOM and DSS.
  • Administration of AB23A and assessment of disease activity, colon tumor load, and tissue injury.
  • Analysis of inflammatory cytokine profiles, signaling pathways (TLR, NF-κB, MAPK), and gut microbiota composition.

Main Results:

  • AB23A intervention significantly alleviated CAC symptoms, including reduced body weight loss, disease activity index, and colon tumor burden.
  • AB23A decreased inflammatory cytokine levels and inhibited the activation of TLR, NF-κB, and MAPK signaling pathways.
  • AB23A treatment promoted gut barrier integrity by up-regulating mucin-2 and tight junction proteins, and favorably altered gut microbiota diversity.

Conclusions:

  • AB23A demonstrates significant potential for the prevention and treatment of colitis-associated cancer.
  • The therapeutic effects of AB23A are mediated through the modulation of inflammatory pathways and the gut microbiome.
  • AB23A represents a promising natural compound for future therapeutic strategies against CAC.