Cabou Cendrine, Burcelin Rémy
INSERM (Institut National de la Sante et de la Recherche Medicale), U1048, Institute of Metabolic and Cardiovascular Diseases Rangueil, University of Toulouse III (Paul-Sabatier), Toulouse, France.
Rev Diabet Stud. 2011 Fall;8(3):418-31. doi: 10.1900/RDS.2011.8.418. Epub 2011 Nov 10.
Glucagon-like peptide 1 (GLP-1) is a gut hormone which directly binds to the GLP-1 receptor located at the surface of the pancreatic β-cells to enhance glucose-induced insulin secretion. In addition to its pancreatic effects, GLP-1 can induce metabolic actions by interacting with its receptors expressed on nerve cells in the gut and the brain. GLP-1 can also be considered as a neuropeptide synthesized by neuronal cells in the brain stem that release the peptide directly into the hypothalamus. In this environment, GLP-1 is assumed to control numerous metabolic and cardiovascular functions such as insulin secretion, glucose production and utilization, and arterial blood flow. However, the exact roles of these two locations in the regulation of glucose homeostasis are not well understood. In this review, we highlight the latest experimental data supporting the role of the gut-brain and brain-periphery axes in the control of glucose homeostasis. We also focus our attention on the relevance of β-cell and brain cell targeting by gut GLP-1 for the regulation of glucose homeostasis. In addition to its action on β-cells, we find that understanding the physiological role of GLP-1 will help to develop GLP-1-based therapies to control glycemia in type 2 diabetes by triggering the gut-brain axis or the brain directly. This pleiotropic action of GLP-1 is an important concept that may help to explain the observation that, during their treatment, type 2 diabetic patients can be identified as 'responders' and 'non-responders'.
胰高血糖素样肽1(GLP-1)是一种肠激素,它直接与位于胰腺β细胞表面的GLP-1受体结合,以增强葡萄糖诱导的胰岛素分泌。除了对胰腺的作用外,GLP-1还可通过与肠道和大脑神经细胞上表达的受体相互作用来诱导代谢作用。GLP-1也可被视为由脑干中的神经元细胞合成的神经肽,这些神经元细胞将该肽直接释放到下丘脑。在这种环境下,GLP-1被认为可控制多种代谢和心血管功能,如胰岛素分泌、葡萄糖生成和利用以及动脉血流。然而,这两个部位在葡萄糖稳态调节中的确切作用尚不完全清楚。在本综述中,我们重点介绍了支持肠-脑轴和脑-外周轴在葡萄糖稳态控制中作用的最新实验数据。我们还将注意力集中在肠道GLP-1靶向β细胞和脑细胞对葡萄糖稳态调节的相关性上。除了其对β细胞的作用外,我们发现了解GLP-1的生理作用将有助于开发基于GLP-1的疗法,通过触发肠-脑轴或直接作用于大脑来控制2型糖尿病患者的血糖水平。GLP-1的这种多效性作用是一个重要概念,可能有助于解释在治疗过程中2型糖尿病患者可被分为“反应者”和“无反应者”这一现象。