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The antipsychotic olanzapine interacts with the gut microbiome to cause weight gain in mouse.
Morgan, Andrew P; Crowley, James J; Nonneman, Randal J; Quackenbush, Corey R; Miller, Cheryl N; Ryan, Allison K; Bogue, Molly A; Paredes, Sur Herrera; Yourstone, Scott; Carroll, Ian M; Kawula, Thomas H; Bower, Maureen A; Sartor, R Balfour; Sullivan, Patrick F.
Afiliación
  • Morgan AP; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Curriculum in Bioinformatics and Computational Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Crowley JJ; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Nonneman RJ; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Quackenbush CR; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Miller CN; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Ryan AK; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Bogue MA; The Jackson Laboratory, Bar Harbor, Maine, United States of America.
  • Paredes SH; Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Curriculum in Bioinformatics and Computational Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Yourstone S; Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Curriculum in Bioinformatics and Computational Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Carroll IM; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Center for Gastrointestinal Biology and Disease, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Kawula TH; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Bower MA; Center for Gastrointestinal Biology and Disease, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Sartor RB; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Center for Gastrointestinal Biology and Disease, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Sullivan PF; Departments of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
PLoS One ; 9(12): e115225, 2014.
Article en En | MEDLINE | ID: mdl-25506936
ABSTRACT
The second-generation antipsychotic olanzapine is effective in reducing psychotic symptoms but can cause extreme weight gain in human patients. We investigated the role of the gut microbiota in this adverse drug effect using a mouse model. First, we used germ-free C57BL/6J mice to demonstrate that gut bacteria are necessary and sufficient for weight gain caused by oral delivery of olanzapine. Second, we surveyed fecal microbiota before, during, and after treatment and found that olanzapine potentiated a shift towards an "obesogenic" bacterial profile. Finally, we demonstrated that olanzapine has antimicrobial activity in vitro against resident enteric bacterial strains. These results collectively provide strong evidence for a mechanism underlying olanzapine-induced weight gain in mouse and a hypothesis for clinical translation in human patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antipsicóticos / Benzodiazepinas / Aumento de Peso / Microbioma Gastrointestinal Límite: Animals Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antipsicóticos / Benzodiazepinas / Aumento de Peso / Microbioma Gastrointestinal Límite: Animals Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos