Regulation of leptin on insulin secretion and sulfonulurea receptor 1 transcription level in isolated rats pancreatic islets

• Published in: Chinese medical journal Vol. 116; no. 6; pp. 868 - 872
• Main Author: 袁莉 安汉祥 邓秀玲 李卓娅
• Format: Journal Article
• Language: English
• Published: China Department of Endocrinology, Union Hospital, Tongji Medical College,Huazhong University of Science and Technology, Wuhan 430022, China%Cancer Research Centre in Germany, Heidelberg 69120, Germany%Immunology Research Institute, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China 01.06.2003
• Subjects: Animals; Butadienes - pharmacology; Cells, Cultured; Dose-Response Relationship, Drug; Insulin - metabolism; Insulin Secretion; Islets of Langerhans - drug effects; Islets of Langerhans - metabolism; leptin; Leptin - pharmacology; Male; Nitriles - pharmacology; Phosphatidylinositol 3-Kinases - physiology; Potassium Channels, Inwardly Rectifying - genetics; Rats; Rats, Sprague-Dawley; RNA, Messenger - analysis; SUR1; 细胞信号转导; 胰岛素分泌; 钾离子通道; insulin secretion; transcription; sulfonulurea receptor; leptin
• ISSN: 0366-6999; 2542-5641

Objective To investigate the regulation of leptin on insulin secretion and expression of ATP-sensitive potassium channel subunit sulfonulurea receptor 1 (SUR1) mRNA, and to determine whether the effects of leptin are mediated through known intracellular signaling transduction.Methods Pancreatic islets were isolated by the collagenase method from male SD rats. The purified islets were incubated with different concentrations of leptin for 2 h in the presence of different concentrations of glucose. Insulin release was measured using radioimmunoassay. Expression of SUR1 mRNA was detected by RT-PCR.Results In the presence of leptin 2 nmol/L, insulin release was significantly inhibited at either 11.1 or 16.7 mmol/L glucose concentration (both P<0. 05), but insulin release was not altered at glucose of 5. 6 mmol/L physiological concentration. The dose-response experiment showed that the maximaleffect of leptin on insulin secretion achieved at 2 nmol/L. Exposure of islets to 2 nmol/L leptin induceda significant increase of SUR1 transcription levels by 71% (P<0. 01 ) at 11.1 mmol/L glucose and by 56% ( P <0.05) at 16.7 mmol/L glucose concentration. Selective phosphatidylinositol 3-kinase ( PI 3-kinase) inhibitor wortmannin significantly prevented the leptin effect on insulin secretion and SUR1 mRNA expression.Conclusions Regulatory effects of leptin on insulin secretion could be biphasic at different concentrations of glucose and leptin. The stimulatory regulation of SUR1 transcription levels may be mediated through activation of PI 3-kinase pathway, which may be a possible mechanism of leptin in regulating insulin secretion.