Porzio O, Marlier L N, Federici M, Hribal M L, Magnaterra R, Lauro D, Fusco A, Sesti G, Borboni P
Department of Internal Medicine, University of Rome Tor Vergata, Italy.
Mol Cell Endocrinol. 1999 Jul 20;153(1-2):155-61. doi: 10.1016/s0303-7207(99)00073-8.
In the present study we examined the effect of sulfonylurea on the expression of the glucose transporter GLUT2 and the glucose phosphorylating enzyme Glucokinase (GK) in betaTC6-F7 cells; furthermore, we studied the modifications induced by sulfonylurea on glucose-responsiveness and -sensitivity. Results demonstrate that sulfonylurea increases GLUT2 and GK mRNA expression after 24 h in a dose-dependent manner. On the contrary, after 48 and 72 h a time-dependent reduction of both GLUT2 and GK mRNA occurs. GLUT2 and GK protein expression follow the same modifications. Therefore, GLUT2 and GK are coordinately regulated by sulfonylurea, probably by a common mechanism. Glucose-induced insulin release is increased by sulfonylurea as well as glucose sensitivity. Our study suggests that short-term effect of sulfonylurea increases while long-term effect reduces the expression of glucose sensing elements. The long-term inhibitory effect on glucose sensing elements would explain the reduced insulin secretion occurring after chronic sulfonylurea treatment.
在本研究中,我们检测了磺脲类药物对βTC6-F7细胞中葡萄糖转运蛋白2(GLUT2)和葡萄糖磷酸化酶葡萄糖激酶(GK)表达的影响;此外,我们研究了磺脲类药物对葡萄糖反应性和敏感性的诱导修饰。结果表明,磺脲类药物在24小时后以剂量依赖的方式增加GLUT2和GK mRNA的表达。相反,在48小时和72小时后,GLUT2和GK mRNA均出现时间依赖性降低。GLUT2和GK蛋白表达呈现相同的变化。因此,GLUT2和GK可能通过共同机制受到磺脲类药物的协同调节。磺脲类药物可增加葡萄糖诱导的胰岛素释放以及葡萄糖敏感性。我们的研究表明,磺脲类药物的短期作用会增加而长期作用会降低葡萄糖感应元件的表达。对葡萄糖感应元件的长期抑制作用可以解释慢性磺脲类药物治疗后胰岛素分泌减少的现象。