PT  - JOURNAL ARTICLE
AU  - Eto, Kazuhiro
AU  - Yamashita, Tokuyuki
AU  - Matsui, Junji
AU  - Terauchi, Yasuo
AU  - Noda, Mitsuhiko
AU  - Kadowaki, Takashi
TI  - Genetic Manipulations of Fatty Acid Metabolism in β-Cells Are Associated With Dysregulated Insulin Secretion
AID  - 10.2337/diabetes.51.2007.S414
DP  - 2002 Dec 01
TA  - Diabetes
PG  - S414--S420
VI  - 51
IP  - suppl 3
4099  - http://diabetes.diabetesjournals.org/content/51/suppl_3/S414.short
4100  - http://diabetes.diabetesjournals.org/content/51/suppl_3/S414.full
SO  - Diabetes2002 Dec 01; 51
AB  - Triacylglyceride (TG) accumulation in pancreatic β-cells is associated with impaired insulin secretion, which is called lipotoxicity. To gain a better understanding of the pathophysiology of lipotoxicity, we generated three models of dysregulated fatty acid metabolism in β-cells. The overexpression of sterol regulatory element binding protein-1c induced lipogenic genes and TG accumulation. Under these conditions, we observed a decrease in glucose oxidation and upregulation of uncoupling protein-2, which might be causally related to the decreased glucose-stimulated insulin secretion. The overexpression of AMP-activated protein kinase was accompanied by decreased lipogenesis, increased fatty acid oxidation, and decreased glucose oxidation; insulin secretions to glucose and depolarization stimuli were decreased, probably because of the decrease in glucose oxidation and cellular insulin content. It was notable that the secretory response to palmitate was blunted, which would suggest a role of the fatty acid synthesis pathway, but not its oxidative pathway in palmitate-stimulated insulin secretion. Finally, we studied islets of PPAR-γ+/− mice that had increased insulin sensitivity and low TG content in white adipose tissue, skeletal muscle, and liver. On a high-fat diet, glucose-stimulated insulin secretion was decreased in association with increased TG content in the islets, which might be mediated through the elevated serum free fatty acid levels and their passive transport into β-cells. These results revealed some aspects about the mechanisms by which alterations of fatty acid metabolism affect β-cell functions.