Metformin and Dipeptidyl Peptidase-4 Inhibitor Differentially Modulate the Intestinal Microbiota and Plasma Metabolome of Metabolically Dysfunctional Mice

Recent evidence indicates that gut microbiota is altered considerably by a variety of commonly prescribed medications. This study assessed the impact of 2 antidiabetic therapeutics on gut microbiota and markers of cardiometabolic disease in metabolically dysfunctional mice. C57BL/6 mice were fed a h...

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Veröffentlicht in:Canadian journal of diabetes 2020-03, Vol.44 (2), p.146-155.e2
Hauptverfasser: Ryan, Paul M., Patterson, Elaine, Carafa, Ilaria, Mandal, Rupasri, Wishart, David S., Dinan, Timothy G., Cryan, John F., Tuohy, Kieran M., Stanton, Catherine, Ross, R. Paul
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Sprache:eng
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Zusammenfassung:Recent evidence indicates that gut microbiota is altered considerably by a variety of commonly prescribed medications. This study assessed the impact of 2 antidiabetic therapeutics on gut microbiota and markers of cardiometabolic disease in metabolically dysfunctional mice. C57BL/6 mice were fed a high-fat diet for 24 weeks while receiving 1 of 2 antidiabetic therapeutics—metformin or dipeptidyl peptidase-4 (DPP-4) inhibitor, PKF-275-055—for the final 12 weeks. Mice were assessed for weight gain, glucose and cholesterol metabolism, and adiposity. In addition, cecal microbiota was analyzed by 16S compositional sequencing, and plasma metabolome was analyzed by liquid chromatography with tandem mass spectrometry. Both therapeutics had similar metabolic effects, attenuating mesenteric adiposity and improving cholesterol metabolism and insulin sensitivity. However, multivariate analyses of microbiota and metabolomics data revealed clear divergence of the therapeutic groups. Although both metformin and PKF-275-055 mice displayed significantly decreased Firmicutes/Bacteroidetes ratios, only metformin harboured metabolic health-associated Akkermansia, Parabacteroides and Christensenella. Paradoxically, metformin also reduced α diversity, a metric frequently associated with host metabolic fitness. PKF-275-055 mice displayed elevated levels of butyrate-producing Ruminococcus and acetogen Dorea, with reduced levels of certain plasma sphingomyelin, phosphatidylcholine and lysophosphatidylcholine entities. In turn, metformin reduced levels of acylcarnitines, a functional group associated with systemic metabolic dysfunction. Finally, several associations were identified between metabolites and altered taxa. This study represents the first direct comparison of the microbiota-modifying effects of metformin and a DPP-4 inhibitor, and proposes several putative microbial targets both in terms of novel therapeutic development and adverse effect prevention. Des données probantes récentes montrent qu'un grand nombre de médicaments souvent prescrits modifient considérablement le microbiote intestinal. La présente étude a permis d’évaluer les effets de 2 traitements antidiabétiques sur le microbiote intestinal et les marqueurs de maladies cardiométaboliques chez des souris ayant un dysfonctionnement métabolique. Les souris C57BL/6 ont été soumises à un régime riche en matières grasses durant 24 semaines, et ont reçu 1 ou 2 traitements antidiabétiques (metformine ou inhibiteur de
ISSN:1499-2671
2352-3840
DOI:10.1016/j.jcjd.2019.05.008