Tolhurst Gwen, Reimann Frank, Gribble Fiona M
Cambridge Institute for Medical Research and Department of Clinical Biochemistry, Addenbrooke's Hospital, Hills Road, Cambridge CB2 0XY, UK.
J Physiol. 2009 Jan 15;587(1):27-32. doi: 10.1113/jphysiol.2008.164012. Epub 2008 Nov 10.
Glucagon-like peptide-1 (GLP-1), released from L-cells in the intestinal epithelium, plays an important role in postprandial glucose homeostasis and appetite control. Following the recent therapeutic successes of antidiabetic drugs aimed at either mimicking GLP-1 or preventing its degradation, attention is now turning towards the L-cell, and addressing whether it would be both possible and beneficial to stimulate the endogenous release of GLP-1 in vivo. Understanding the mechanisms underlying GLP-1 release from L-cells is key to this type of approach, and the use of cell line models has led to the identification of a variety of pathways that may underlie the physiological responses of L-cells to food ingestion. This review focuses on our current understanding of the signalling mechanisms that underlie L-cell nutrient responsiveness.
胰高血糖素样肽-1(GLP-1)由肠道上皮的L细胞释放,在餐后血糖稳态和食欲控制中发挥重要作用。随着近期旨在模拟GLP-1或防止其降解的抗糖尿病药物取得治疗成功,现在人们的注意力转向了L细胞,并探讨在体内刺激GLP-1内源性释放是否可行且有益。了解L细胞释放GLP-1的潜在机制是这类方法的关键,细胞系模型的使用已促使人们识别出多种可能构成L细胞对食物摄入生理反应基础的途径。本综述重点关注我们目前对L细胞营养反应性潜在信号机制的理解。