Sexual dimorphism of adipose and hepatic aquaglyceroporins in health and metabolic disorders
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Frontiers Media
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Gender differences in the relative risk of developing metabolic complications, such as
insulin resistance or non-alcoholic fatty liver disease (NAFLD), have been reported. The
deregulation of glycerol metabolism partly contributes to the onset of these metabolic
diseases, since glycerol constitutes a key substrate for the synthesis of triacylglycerols
(TAGs) as well as for hepatic gluconeogenesis. The present mini-review covers the sexrelated differences in glycerol metabolism and aquaglyceroporins (AQPs) and its impact
in the control of adipose and hepatic fat accumulation as well as in whole-body glucose
homeostasis. Plasma glycerol concentrations are increased in women compared to men
probably due to the higher lipolytic rate and larger AQP7 amounts in visceral fat as well
as the well-known sexual dimorphism in fat mass with women showing higher adiposity.
AQP9 represents the primary route for glycerol uptake in hepatocytes, where glycerol is
converted by the glycerol-kinase enzyme into glycerol-3-phosphate, a key substrate for
de novo synthesis of glucose and TAG. In spite of showing similar hepatic AQP9 protein,
women exhibit lower hepatocyte glycerol permeability than men, which might contribute
to their lower prevalence of insulin resistance and NAFLD.
Para citar este articulo: Rodríguez A, Marinelli RA, Tesse A, Frühbeck G and Calamita G (2015) Sexual Dimorphism of Adipose and Hepatic Aquaglyceroporins in Health and Metabolic Disorders. Front. Endocrinol. 6:171. doi: 10.3389/fendo.2015.00171
Para citar este articulo: Rodríguez A, Marinelli RA, Tesse A, Frühbeck G and Calamita G (2015) Sexual Dimorphism of Adipose and Hepatic Aquaglyceroporins in Health and Metabolic Disorders. Front. Endocrinol. 6:171. doi: 10.3389/fendo.2015.00171
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