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Elucidating the mechanisms by which disulfiram protects against obesity and metabolic syndrome.
Bernier, Michel; Harney, Dylan; Koay, Yen Chin; Diaz, Antonio; Singh, Abhishek; Wahl, Devin; Pulpitel, Tamara; Ali, Ahmed; Guiterrez, Vince; Mitchell, Sarah J; Kim, Eun-Young; Mach, John; Price, Nathan L; Aon, Miguel A; LeCouteur, David G; Cogger, Victoria C; Fernandez-Hernando, Carlos; O'Sullivan, John; Larance, Mark; Cuervo, Ana Maria; de Cabo, Rafael.
Afiliación
  • Bernier M; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Harney D; Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006 Australia.
  • Koay YC; Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006 Australia.
  • Diaz A; Heart Research Institute, The University of Sydney, Sydney, NSW 2042 Australia.
  • Singh A; Department of Developmental and Molecular Biology, Institute for Aging Studies, Albert Einstein College of Medicine, New York, NY 10461 USA.
  • Wahl D; Vascular Biology and Therapeutics Program, Integrative Cell Signaling and Neurobiology of Metabolism Program, Department of Comparative Medicine, Department of Pathology, Yale University School of Medicine, New Haven, CT 06510 USA.
  • Pulpitel T; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Ali A; Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006 Australia.
  • Guiterrez V; Ageing and Alzheimer's Institute, ANZAC Research Institute, Concord Clinical School/Sydney Medical School, Concord, NSW 2139 Australia.
  • Mitchell SJ; Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006 Australia.
  • Kim EY; Ageing and Alzheimer's Institute, ANZAC Research Institute, Concord Clinical School/Sydney Medical School, Concord, NSW 2139 Australia.
  • Mach J; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Price NL; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Aon MA; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • LeCouteur DG; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Cogger VC; Functional Genomics Research Center, KRIBB, Daejeon, 305-806 Republic of Korea.
  • Fernandez-Hernando C; Kolling Institute of Medical Research and Sydney Medical School, University of Sydney, Sydney, NSW 2064 Australia.
  • O'Sullivan J; Vascular Biology and Therapeutics Program, Integrative Cell Signaling and Neurobiology of Metabolism Program, Department of Comparative Medicine, Department of Pathology, Yale University School of Medicine, New Haven, CT 06510 USA.
  • Larance M; Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
  • Cuervo AM; Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006 Australia.
  • de Cabo R; Ageing and Alzheimer's Institute, ANZAC Research Institute, Concord Clinical School/Sydney Medical School, Concord, NSW 2139 Australia.
NPJ Aging Mech Dis ; 6: 8, 2020.
Article en En | MEDLINE | ID: mdl-32714562
ABSTRACT
There is an unmet need and urgency to find safe and effective anti-obesity interventions. Our recent study in mice fed on obesogenic diet found that treatment with the alcohol aversive drug disulfiram reduced feeding efficiency and led to a decrease in body weight and an increase in energy expenditure. The intervention with disulfiram improved glucose tolerance and insulin sensitivity, and mitigated metabolic dysfunctions in various organs through poorly defined mechanisms. Here, integrated analysis of transcriptomic and proteomic data from mouse and rat livers unveiled comparable signatures in response to disulfiram, revealing pathways associated with lipid and energy metabolism, redox, and detoxification. In cell culture, disulfiram was found to be a potent activator of autophagy, the malfunctioning of which has negative consequences on metabolic regulation. Thus, repurposing disulfiram may represent a potent strategy to combat obesity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: NPJ Aging Mech Dis Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: NPJ Aging Mech Dis Año: 2020 Tipo del documento: Article
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