Dehydroepiandrosterone sulfate and β-cell function -: Enhanced glucose-induced insulin secretion and altered gene expression in rodent pancreatic β-cells

Administration of dehydroepiandrosterone (DHEA), or its sulfated form (DHEAS), controls hyperglycemia in diabetic rodents without directly altering insulin sensitivity. me show that DHEAS enhanced glucose-stimulated insulin secretion when administered in vivo to rats or in vitro to beta -cell lines, without changing cellular insulin content, insulin secretion increased from 3 days of steroid exposure in vitro, suggesting that DHEAS did not directly activate the secretory processes. DHEAS selectively increased the beta -cell mRNA expression of acyl CoA synthetase-2 and peroxisomal acyl CoA oxidase in a time-dependent manner. Although DHEAS is a peroxisomal proliferator, it did not alter the mRNA expression of peroxisomal proliferator-activated receptor (PPAR) alpha or beta, or enhance the activity of transfected PPAR alpha, beta, or gamma in vitro. Thus, DHEAS directly affected the beta -cell to enhance glucose-stimulated insulin secretion and increased the mRNA expression of specific beta -cell mitochondrial and peroxisomal lipid metabolic enzymes. This effect of DHEAS on insulin secretion may contribute to the amelioration of hyperglycemia seen in various rodent models of diabetes.