Department of Laboratory Medicine and Pathobiology, Banting and Best Diabetes Centre, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Vitam Horm. 2010;84:1-20. doi: 10.1016/B978-0-12-381517-0.00001-1.
The incretin hormones glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are essential components in the regulation of blood glucose levels in mammals. These two incretins are produced by evolutionarily related genes and these hormones show similarity in sequence as both are glucagon-like sequences. Genes for these hormones have been identified in a number of diverse vertebrate species indicating that they originated prior to the earliest divergences of vertebrate species. However, analysis of functional and sequence data suggest that each of these hormones acquired incretin activity independently, and only since the divergence of tetrapods from fish. Not only are the hormones related, but so are their receptors. Like the hormones, the incretin action of the receptors is not a product of a shared common ancestral history, as the receptors for GLP-1 and GIP are not most closely related. Further study of the physiological functions of GLP-1 and GIP in additional vertebrates is required to better understand the origin of incretin action.
肠促胰岛素激素胰高血糖素样肽-1 (GLP-1) 和葡萄糖依赖性胰岛素释放肽 (GIP) 是哺乳动物血糖调节的重要组成部分。这两种肠促胰岛素由进化上相关的基因产生,它们在序列上具有相似性,因为它们都是胰高血糖素样序列。这些激素的基因已在许多不同的脊椎动物物种中被鉴定出来,这表明它们起源于脊椎动物最早分化之前。然而,对功能和序列数据的分析表明,这两种激素的肠促胰岛素活性是独立获得的,而且仅在从鱼类分化出四足动物之后。不仅激素是相关的,它们的受体也是如此。与激素一样,受体的肠促胰岛素作用不是共享共同祖先历史的产物,因为 GLP-1 和 GIP 的受体并不是最密切相关的。需要进一步研究 GLP-1 和 GIP 在其他脊椎动物中的生理功能,以更好地理解肠促胰岛素作用的起源。