Drucker D J
Department of Medicine, the Toronto Hospital, Banting and Best Diabetes Centre, University of Toronto, Ontario, Canada.
Diabetes. 1998 Feb;47(2):159-69. doi: 10.2337/diab.47.2.159.
Proglucagon contains the sequence of two glucagon-like peptides, GLP-1 and GLP-2, secreted from enteroendocrine cells of the small and large intestine. GLP-1 lowers blood glucose in both NIDDM and IDDM patients and may be therapeutically useful for treatment of patients with diabetes. GLP-1 regulates blood glucose via stimulation of glucose-dependent insulin secretion, inhibition of gastric emptying, and inhibition of glucagon secretion. GLP-1 may also regulate glycogen synthesis in adipose tissue and muscle; however, the mechanism for these peripheral effects remains unclear. GLP-1 is produced in the brain, and intracerebroventricular GLP-1 in rodents is a potent inhibitor of food and water intake. The short duration of action of GLP-1 may be accounted for in part by the enzyme dipeptidyl peptidase 4 (DPP-IV), which cleaves GLP-1 at the NH2-terminus; hence GLP-1 analogs or the lizard peptide exendin-4 that are resistant to DPP-IV cleavage may be more potent GLP-1 molecules in vivo. GLP-2 has recently been shown to display intestinal growth factor activity in rodents, raising the possibility that GLP-2 may be therapeutically useful for enhancement of mucosal regeneration in patients with intestinal disease. This review discusses recent advances in our understanding of the biological activity of the glucagon-like peptides.
胰高血糖素原包含两种胰高血糖素样肽即GLP-1和GLP-2的序列,它们由小肠和大肠的肠内分泌细胞分泌。GLP-1可降低非胰岛素依赖型糖尿病(NIDDM)和胰岛素依赖型糖尿病(IDDM)患者的血糖,可能对糖尿病患者的治疗有用。GLP-1通过刺激葡萄糖依赖性胰岛素分泌、抑制胃排空和抑制胰高血糖素分泌来调节血糖。GLP-1还可能调节脂肪组织和肌肉中的糖原合成;然而,这些外周效应的机制尚不清楚。GLP-1在大脑中产生,啮齿动物脑室内的GLP-1是食物和水摄入的有效抑制剂。GLP-1作用持续时间短可能部分是由二肽基肽酶4(DPP-IV)所致,该酶在NH2末端切割GLP-1;因此,对DPP-IV切割具有抗性的GLP-1类似物或蜥蜴肽艾塞那肽-4在体内可能是更有效的GLP-1分子。最近研究表明GLP-2在啮齿动物中具有肠道生长因子活性,这增加了GLP-2可能对肠道疾病患者黏膜再生增强治疗有用的可能性。本文综述了我们对胰高血糖素样肽生物学活性认识的最新进展。