Thorens Bernard
Institut de Physiologie, 27, rue du Bugnon, 1005 Lausanne, Suisse.
Med Sci (Paris). 2003 Aug-Sep;19(8-9):860-3. doi: 10.1051/medsci/20031989860.
Nutrient ingestion triggers a complex hormonal response aimed at stimulating glucose utilization in liver, muscle and adipose tissue to minimize the raise in blood glucose levels. Insulin secretion by pancreatic beta cells plays a major role in this response. Although the beta cell secretory response is mainly controlled by blood glucose levels, gut hormones secreted in response to food intake have an important role in potentiating glucose-stimulated insulin secretion. These gluco-incretin hormones are GLP-1 (glucagon-like peptide-1) and GIP (gluco-dependent insulinotropic polypeptide). Their action on pancreatic beta cells depends on binding to specific G-coupled receptors linked to activation of the adenylyl cyclase pathway. In addition to their effect on insulin secretion both hormones also stimulate insulin production at the transcriptional and translational level and positively regulate beta cell mass. Because the glucose-dependent insulinotropic action of GLP-1 is preserved in type 2 diabetic patients, this peptide is now developed as a novel therapeutic drug for this disease.
营养物质的摄入会引发复杂的激素反应,旨在刺激肝脏、肌肉和脂肪组织对葡萄糖的利用,以尽量减少血糖水平的升高。胰腺β细胞分泌胰岛素在这一反应中起主要作用。虽然β细胞的分泌反应主要受血糖水平控制,但进食后分泌的肠道激素在增强葡萄糖刺激的胰岛素分泌方面发挥着重要作用。这些葡萄糖促胰岛素分泌激素是胰高血糖素样肽-1(GLP-1)和葡萄糖依赖性促胰岛素多肽(GIP)。它们对胰腺β细胞的作用取决于与特定的G偶联受体结合,这些受体与腺苷酸环化酶途径的激活有关。除了对胰岛素分泌的影响外,这两种激素还在转录和翻译水平上刺激胰岛素生成,并对β细胞数量起到正向调节作用。由于GLP-1的葡萄糖依赖性促胰岛素作用在2型糖尿病患者中得以保留,这种肽目前正被开发为治疗该疾病的新型药物。