Physiology and Pharmacology of the Enteroendocrine Hormone Glucagon-Like Peptide-2

被引:259
作者
Drucker, Daniel J. [1 ]
Yusta, Bernardo [1 ]
机构
[1] Univ Toronto, Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Dept Med, Toronto, ON M5G 1X5, Canada
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 76 | 2014年 / 76卷
关键词
G protein-coupled receptor; GLP-1; glucagon; intestinal failure; peptide; growth factor; SHORT-BOWEL SYNDROME; GROWTH-FACTOR-I; FACTOR RECEPTOR INHIBITOR; INTESTINAL BLOOD-FLOW; GLP-2; RECEPTOR; ENTERIC NEURONS; BONE-RESORPTION; INTESTINOTROPHIC PEPTIDE; ANTIINFLAMMATORY ACTIONS; LIPID ABSORPTION;
D O I
10.1146/annurev-physiol-021113-170317
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Glucagon-like peptide-2 (GLP-2) is a 33-amino-acid proglucagon-derived peptide secreted from enteroendocrine L cells. GLP-2 circulates at low basal levels in the fasting period, and plasma levels rise rapidly after food ingestion. Renal clearance and enzymatic inactivation control the elimination of bioactive GLP-2. GLP-2 increases mesenteric blood flow and activates proabsorptive pathways in the gut, facilitating nutrient absorption. GLP-2 also enhances gut barrier function and induces proliferative and cytoprotective pathways in the small bowel. The actions of GLP-2 are transduced via a single G protein-coupled receptor (GLP-2R), expressed predominantly within the gastrointestinal tract. Disruption of GLP-2R signaling increases susceptibility to gut injury and impairs the adaptive mucosal response to refeeding. Sustained augmentation of GLP-2R signaling reduces the requirement for parenteral nutrition in human subjects with short-bowel syndrome. Hence GLP-2 integrates nutrient-derived signals to optimize mucosal integrity and energy absorption.
引用
收藏
页码:561 / 583
页数:23
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