Xylo-Oligosaccharides in Prevention of Hepatic Steatosis and Adipose Tissue Inflammation : Associating Taxonomic and Metabolomic Patterns in Fecal Microbiomes with Biclustering
Hintikka, J., Lensu, S., Mäkinen, E., Karvinen, S., Honkanen, M., Lindén, J., Garrels, T., Pekkala, S., & Lahti, L. (2021). Xylo-Oligosaccharides in Prevention of Hepatic Steatosis and Adipose Tissue Inflammation : Associating Taxonomic and Metabolomic Patterns in Fecal Microbiomes with Biclustering. International Journal of Environmental Research and Public Health, 18(8), Article 4049. https://doi.org/10.3390/ijerph18084049
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2021Copyright
© 2021 by the authors. Licensee MDPI, Basel, Switzerland
We have shown that prebiotic xylo-oligosaccharides (XOS) increased beneficial gut microbiota (GM) and prevented high fat diet-induced hepatic steatosis, but the mechanisms associated with these effects are not clear. We studied whether XOS affects adipose tissue inflammation and insulin signaling, and whether the GM and fecal metabolome explain associated patterns. XOS was supplemented or not with high (HFD) or low (LFD) fat diet for 12 weeks in male Wistar rats (n = 10/group). Previously analyzed GM and fecal metabolites were biclustered to reduce data dimensionality and identify interpretable groups of co-occurring genera and metabolites. Based on our findings, biclustering provides a useful algorithmic method for capturing such joint signatures. On the HFD, XOS-supplemented rats showed lower number of adipose tissue crown-like structures, increased phosphorylation of AKT in liver and adipose tissue as well as lower expression of hepatic miRNAs. XOS-supplemented rats had more fecal glycine and less hypoxanthine, isovalerate, branched chain amino acids and aromatic amino acids. Several bacterial genera were associated with the metabolic signatures. In conclusion, the beneficial effects of XOS on hepatic steatosis involved decreased adipose tissue inflammation and likely improved insulin signaling, which were further associated with fecal metabolites and GM.
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https://converis.jyu.fi/converis/portal/detail/Publication/66397002
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Academy Research Fellow, AoFAdditional information about funding
This study was financially supported by the Academy of Finland Researcher fellowship for S.P. (grant ID 308042) and by the ERVA funding of The Hospital District of Southwest Finland for S.P. L.L. was funded by Academy of Finland Researcher fellowship (grant ID 295741). The foundation of Jenny and Antti Wihuri and the Central Finland Regional fund of the Finnish Cultural Foundation are acknowledged for their personal grants to S.L. to perform this study. ...License
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