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Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism

Yanyan Gao et al · Frontiers Media S.A · 2026

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IntroductionMetabolism-associated fatty liver disease (MAFLD) has emerged as a severe worldwide public health burden with insufficient available clinical therapeutic strategies, which underscores the urgent demand for safe, natural dietary interventions. Raspberry (Rubus idaeus L.), a typical food-medicine homologous fruit abundant in diverse bioactive components including anthocyanins, flavonoids and polysaccharides, possesses prominent nutritional and medicinal potential.MethodsIn this study, raspberry aqueous extract (RE) was prepared to comprehensively investigate its ameliorative effects and underlying molecular mechanisms against MAFLD. MAFLD animal model was established in C57BL/6 mice via 12-week high-fat diet (HFD) feeding. From the 9th week, model mice were intragastrically administered with RE at doses of 1 g/kg/d and 2 g/kg/d for continuous intervention. Integrated multi-omics analyses including 16S rRNA microbial sequencing, serum/hepatic biochemical detection, histopathological examination, in vivo microbial colonization assay, and in vitro cellular and metabolomic experiments were performed to systematically clarify the regulatory mechanism.ResultsRE treatment markedly improved the core pathological phenotypes of MAFLD mice, and significantly mitigated hepatic steatosis and hepatocellular injury. 16S rRNA sequencing demonstrated that RE remodeled the gut microbial dysbiosis, specifically elevating the abundance of beneficial genus Ileibacterium and suppressing pathogenic microbial taxa. Meanwhile, RE strengthened intestinal mucosal barrier integrity by upregulating tight junction protein expression, and activated hepatic purine metabolic reprogramming to boost the levels of critical metabolites including inosine and ADP. Spearman correlation analysis verified the significantly positive correlation between Ileibacterium abundance and hepatic inosine content, and both factors were closely correlated with the remission of MAFLD pathological indicators. In vivo colonization experiments further validated that Ileibacterium intervention alone remarkably alleviated hepatic lipid deposition and liver damage in MAFLD mice. In vitro strain metabolomics confirmed that Ileibacterium could directly biosynthesize and secrete inosine extracellularly. Furthermore, in vitro AML12 hepatocyte experiments revealed that 100 μM inosine remarkably relieved palmitic acid-induced lipotoxicity via reducing intracellular lipid overload, reactive oxygen species (ROS) accumulation and mitochondrial dysfunction, alongside modulating the expression of lipid metabolism, inflammatory and autophagy-related genes.DiscussionCollectively, our results elucidate that raspberry aqueous extract alleviates experimental MAFLD through the gut microbiota-purine metabolism-inosine regulatory axis, in which Ileibacterium and inosine act as the core synergistic mediators. This study provides solid preclinical experimental evidence for the development and application of raspberry as a promising functional food for the prevention and nutritional intervention of MAFLD.

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APA 7

al, Y. G. E. (2026). Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism. https://doi.org/10.3389/fnut.2026.1818086

MLA

al, Yanyan Gao et. "Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism." 2026. https://doi.org/10.3389/fnut.2026.1818086.

Chicago

al, Yanyan Gao et. 2026. "Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism.". https://doi.org/10.3389/fnut.2026.1818086.

Harvard

al, Y. G. E. 2026, Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism, Frontiers Media S.A, available at: https://doi.org/10.3389/fnut.2026.1818086 [Accessed 7 Aug. 2026].

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Titolo
Raspberry aqueous extract ameliorates MAFLD in mice by regulating gut microbiota and purine metabolism
Autore / collaboratori
Yanyan Gao et al
Editore
Frontiers Media S.A
Anno di pubblicazione
2026
ISSN
2296-861X
ISSN
2296-861X
Lingua
Inglés

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