6533b851fe1ef96bd12a9858

RESEARCH PRODUCT

Prebiotic Xylo-oligosaccharides Targeting Faecalibacterium prausnitzii Prevent High Fat Diet-induced Hepatic Steatosis in Rats

Anastasiia DriuchinaEveliina MunukkaMarja TiirolaBaoru YangSanna LensuMaarit LehtiWisam SaleemLeo LahtiJere LindénRaghunath PariyaniSatu PekkalaElina Mäkinen

subject

biologyChemistryPrebioticmedicine.medical_treatmentdigestive oral and skin physiologyFatty livergastroenterologynutritional and metabolic diseasesfood and beveragesFaecalibacterium prausnitziiHigh fat dietMetabolismGut floraMitochondrionmedicine.diseasebiology.organism_classificationdigestive system3. Good healthmedicineFood scienceSteatosis

description

Understanding the importance of gut microbiota (GM) in non-alcoholic fatty liver disease (NAFLD) has raised the hope for therapeutic microbes. We have shown that high hepatic fat associated with low abundance of Faecalibacterium prausnitzii in humans and further, administration of F. prausnitzii prevented NAFLD in mice. Here, we aimed to target F. prausnitzii by prebiotic xylo-oligosaccharides (XOS) to treat NAFLD. First, the effect of XOS on F. prausnitzii growth was assessed in vitro. Then, XOS was supplemented or not with high (HFD) or low (LFD) fat-diet for 12-weeks in Wistar rats (n=10/group). XOS increased F. prausnitzii growth having only minor impact on the GM composition. When supplemented with HFD, XOS prevented hepatic steatosis. The underlying mechanisms involved enhanced hepatic β-oxidation and mitochondrial respiration. 1H-NMR analysis of caecal metabolites showed that compared to HFD, LFD group had healthier caecal short-chain fatty acid profile and the combination of HFD and XOS was associated with reduced caecal isovalerate and tyrosine, metabolites previously linked to NAFLD. Caecal branched-chain fatty acids associated positively and butyrate negatively with hepatic triglycerides. In conclusion, our study identifies F. prausnitzii as a possible target to treat NAFLD with XOS. The underlying preventive mechanisms involved improved hepatic oxidative metabolism.

https://doi.org/10.20944/preprints202009.0241.v1