Risperidone-induced weight gain is mediated through shifts in the gut microbiome and suppression of energy expenditure

Risperidone is a second-generation antipsychotic that causes weight gain. We hypothesized that risperidone-induced shifts in the gut microbiome are mechanistically involved in its metabolic consequences. Wild-type female C57BL/6J mice treated with risperidone (80μg/day) exhibited significant excess...

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Veröffentlicht in:EBioMedicine 2015-11, Vol.2 (11), p.1725-1734
Hauptverfasser: Bahr, Sarah M., Weidemann, Benjamin J., Castro, Ana N., Walsh, John W., deLeon, Orlando, Burnett, Colin M.L., Pearson, Nicole A., Murry, Daryl J., Grobe, Justin L., Kirby, John R.
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Sprache:eng
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Zusammenfassung:Risperidone is a second-generation antipsychotic that causes weight gain. We hypothesized that risperidone-induced shifts in the gut microbiome are mechanistically involved in its metabolic consequences. Wild-type female C57BL/6J mice treated with risperidone (80μg/day) exhibited significant excess weight gain, due to reduced energy expenditure, which correlated with an altered gut microbiome. Fecal transplant from risperidone-treated mice caused a 16% reduction in total resting metabolic rate in naïve recipients, attributable to suppression of non-aerobic metabolism. Risperidone inhibited growth of cultured fecal bacteria grown anaerobically more than those grown aerobically. Finally, transplant of the fecal phage fraction from risperidone-treated mice was sufficient to cause excess weight gain in naïve recipients, again through reduced energy expenditure. Collectively, these data highlight a major role for the gut microbiome in weight gain following chronic use of risperidone, and specifically implicates the modulation of non-aerobic resting metabolism in this mechanism. •Risperidone-induced weight gain correlates with an altered gut microbiome.•Risperidone-induced weight gain occurs due to suppressed energy expenditure.•Transfer of risperidone-treated microbiota or phage suppresses energy expenditure.•Reduction in energy expenditure is attributable to non-aerobic resting metabolism.•Transfer of risperidone-treated microbiota suppresses non-aerobic resting metabolism. Risperidone is increasingly used for psychiatric disorders and is known to cause robust weight gain in humans. This study demonstrates that risperidone-induced weight gain correlates with alterations in the bacterial composition of the gut in mice. The observed weight gain is mediated through suppression of energy expenditure, specifically by reducing non-aerobic resting metabolic rate. The effect can be reproduced by transferring the gut microbiota or associated bacteriophage (bacterial viruses) from risperidone-treated animals to naïve animals. Thus, gut bacteria and their associated viruses can affect changes in resting metabolic rates leading to weight gain.
ISSN:2352-3964
2352-3964
DOI:10.1016/j.ebiom.2015.10.018