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Indole-3-Propionic Acid Alleviates Metabolic Dysfunction-Associated Fatty Liver Disease via AHR/AMPK Signaling Activation.

Created on 08 Aug 2026

Authors

Yanting Huang, Meimei Yu, Jiaxin Lu, Chujun Lin, Shuhuan Li, Yalin Chen, Xin Chen, Hongliang Xue, Jing Chen, Lijie Su

Published in

Food science & nutrition. Volume 14. Issue 8. Pages e72206. Epub Aug 07, 2026.

Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) is a health problem worthy of attention worldwide, characterized by excessive lipid accumulation in the liver. Previous studies have shown that indole-3-propionic acid (IPA) can ameliorate MAFLD; however, the regulatory mechanism by which IPA affects lipid synthesis requires further investigation. In vitro, FFA-induced HepG2 cells were treated with IPA (15-35 μM), and hepatic lipid accumulation was evaluated by Oil Red O staining. RNA-seq and Western blotting were employed to analyze AHR/AMPK signaling activation, and pharmacological inhibitors and agonists targeting AHR and AMPK were applied to explore the regulatory mechanism of IPA on lipid deposition. In vivo, C57BL/6J mice on a high-fat diet received 50 mg/kg IPA for 16 weeks, followed by histopathological evaluation and assessment of AHR/AMPK pathway activation. Results showed that IPA dose-dependently reduced lipid deposition in HepG2 cells. IPA inhibited lipid synthesis by activating AHR (inducing CYP1A1 expression and nuclear translocation) and promoting AMPK phosphorylation, thereby downregulating SREBP-1c and FAS expression. Pharmacological experiments demonstrated that IPA-induced AMPK activation was dependent on AHR nuclear translocation. Moreover, phosphorylated AMPK further promoted AHR nuclear translocation, indicating the existence of a potential bidirectional crosstalk between AHR and AMPK. In animal studies, IPA mitigated HFD-induced hepatic steatosis through activation of the AHR/AMPK signaling pathways. In conclusion, indole-3-propionic acid may alleviate MAFLD by ameliorating high-fat diet-induced hepatic lipid deposition through AHR/AMPK signaling activation.

PMID:
42569087
Bibliographic data and abstract were imported from PubMed on 08 Aug 2026.

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