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      Prevalent role of the insulin receptor isoform A in the regulation of hepatic glycogen metabolism in hepatocytes and in mice.

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          Abstract

          In the postprandial state, the liver regulates glucose homeostasis by glucose uptake and conversion to glycogen and lipids. Glucose and insulin signalling finely regulate glycogen synthesis through several mechanisms. Glucose uptake in hepatocytes is favoured by the insulin receptor isoform A (IRA), rather than isoform B (IRB). Thus, we hypothesised that, in hepatocytes, IRA would increase glycogen synthesis by promoting glucose uptake and glycogen storage.

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          Author and article information

          Journal
          Diabetologia
          Diabetologia
          Springer Nature
          1432-0428
          0012-186X
          Dec 2016
          : 59
          : 12
          Affiliations
          [1 ] Department of Biochemistry and Molecular Biology II, School of Pharmacy, Complutense University of Madrid, Madrid, 28040, Spain.
          [2 ] Mechanisms of Insulin Resistance (MOIR) Consortium, Comunidad de Madrid, Madrid, Spain.
          [3 ] Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Health Institute Carlos III (ISCIII), Spain.
          [4 ] Division of Hepatology and Gene Therapy, Center for Applied Medical Research, University of Navarra, Pamplona, Navarra, Spain.
          [5 ] Department of Biochemistry and Molecular Biology II, School of Pharmacy, Complutense University of Madrid, Madrid, 28040, Spain. oescriba@ucm.es.
          [6 ] Mechanisms of Insulin Resistance (MOIR) Consortium, Comunidad de Madrid, Madrid, Spain. oescriba@ucm.es.
          [7 ] Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Health Institute Carlos III (ISCIII), Spain, . oescriba@ucm.es.
          Article
          10.1007/s00125-016-4088-z
          10.1007/s00125-016-4088-z
          27600278
          938525d2-ede8-41c1-a21f-055471f129b4
          History

          Adeno-associated viruses,Glucose intolerance,Glycogen metabolism,Insulin receptor isoforms,Liver,Type 2 diabetes mellitus

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