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Revisiting the Role of Valeric Acid in Manipulating Ulcerative Colitis
Moting Liu1,2, Yao Zhang3, Jia Liu4
1Laboratory of Anti-inflammation and Immunopharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Valeric acid (VA), a short-chain fatty acid (SCFA), shows therapeutic potential for ulcerative colitis (UC). VA treatment suppressed inflammation in UC models by modulating macrophage activation and cytokine production, suggesting its use as a novel UC treatment.
Area of Science:
- Gastroenterology
- Immunology
- Microbiology
Background:
- Ulcerative colitis (UC) involves complex interactions of inflammation, epithelial dysfunction, immune responses, and gut dysbiosis.
- The role of valeric acid (VA), a short-chain fatty acid (SCFA), in UC pathogenesis is not fully understood.
Purpose of the Study:
- To investigate the pathological role and underlying mechanisms of VA in ulcerative colitis.
- To evaluate the therapeutic potential of VA in UC models.
Main Methods:
- Analysis of SCFA levels in human UC patients and murine colitis models.
- Intervention with VA in murine colitis models and macrophage adoptive transfer experiments.
- Assessment of macrophage activation and inflammatory markers like interleukin-6 (IL-6).
Main Results:
- Alterations in SCFAs, including VA, were observed in UC patients and models.
- VA levels negatively correlated with UC disease severity, monocyte population, and IL-6 levels.
- VA treatment suppressed LPS-activated immune cells and ameliorated DSS-induced colitis by upregulating GPR41/GPR43 and modulating IL-6 production.
Conclusions:
- VA plays a pathological role in modulating macrophage activation in UC.
- VA demonstrates potential as an effective therapeutic agent for ulcerative colitis.
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