Department of Endocrinology and Metabolism, Aristotle University of Thessaloniki, Greece.
Vitam Horm. 2010;84:185-201. doi: 10.1016/B978-0-12-381517-0.00006-0.
Glucose-dependent insulinotropic peptide (GIP) and glucagon-like peptide-1 (GLP-1) are potent stimulators of glucose-dependent insulin secretion, a phenomenon known as incretin effect. After food ingestion, the circulating levels of GIP and GLP-1 rise more quickly than could be explained by the arrival of unabsorbed nutrients that have a direct stimulatory effect on K- and L-cells. Previous studies have thoroughly investigated the possible role of the autonomic nervous system on GIP secretion, demonstrating conflicting results. Recent data from intracerebroventricular infusions of different neuropeptides that participate in the overall regulation of energy homeostasis, suggest the possible existence of additional neuroendocrine mechanisms that may contribute to a central regulation of GIP secretion.
葡萄糖依赖性胰岛素促泌肽(GIP)和胰高血糖素样肽-1(GLP-1)是葡萄糖依赖性胰岛素分泌的有力刺激物,这种现象被称为肠促胰岛素效应。进食后,循环中的 GIP 和 GLP-1 水平上升速度比未被吸收的营养物质直接刺激 K 和 L 细胞所能解释的更快。先前的研究已经彻底研究了自主神经系统对 GIP 分泌的可能作用,结果相互矛盾。最近,通过对参与能量平衡整体调节的不同神经肽的脑室内输注的研究数据,提示可能存在其他神经内分泌机制,这可能有助于对 GIP 分泌进行中枢调节。