| Literature DB >> 24899308 |
Rachel J Perry1, Varman T Samuel2, Kitt F Petersen3, Gerald I Shulman4.
Abstract
Non-alcoholic fatty liver disease and its downstream sequelae, hepatic insulin resistance and type 2 diabetes, are rapidly growing epidemics, which lead to increased morbidity and mortality rates, and soaring health-care costs. Developing interventions requires a comprehensive understanding of the mechanisms by which excess hepatic lipid develops and causes hepatic insulin resistance and type 2 diabetes. Proposed mechanisms implicate various lipid species, inflammatory signalling and other cellular modifications. Studies in mice and humans have elucidated a key role for hepatic diacylglycerol activation of protein kinase Cε in triggering hepatic insulin resistance. Therapeutic approaches based on this mechanism could alleviate the related epidemics of non-alcoholic fatty liver disease and type 2 diabetes.Entities:
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Year: 2014 PMID: 24899308 PMCID: PMC4489847 DOI: 10.1038/nature13478
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962