THE EFFECTS OF GLUCAGON-LIKE PEPTIDE-I (GLP-I) ON HORMONE-SECRETION FROM ISOLATED HUMAN PANCREATIC-ISLETS

被引:59
作者
FEHMANN, HC [1 ]
HERING, BJ [1 ]
WOLF, MJ [1 ]
BRANDHORST, H [1 ]
BRANDHORST, D [1 ]
BRETZEL, RG [1 ]
FEDERLIN, K [1 ]
GOKE, B [1 ]
机构
[1] UNIV GIESSEN,DEPT MED,GIESSEN,GERMANY
关键词
GLUCAGON-LIKE PEPTIDE-I(GLP-I); HORMONE SECRETION; HUMAN PANCREATIC ISLETS; INSULIN; GLUCAGON; SOMATOSTATIN;
D O I
10.1097/00006676-199508000-00014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Glucagon-like peptide-I (GLP-I) is a potent incretin hormone that is now considered as a new therapeutic tool in the treatment of diabetes mellitus. In this study we characterized the effects of GLP-I on peptide hormone release from isolated human pancreatic islets. GLP-I stimulated insulin release in the presence of 10 mM glucose (2.8 mM glucose, 100%; 10 mM glucose, 166%; 10 mM glucose + 10 nM GLP-I, 222%) but had only a weak insulinotropic effect (128%) at 2.8 mM glucose. Glucagon release was inhibited by 10 mM glucose (2.8 mM glucose, 100%; 10 mM glucose, 72%) and by 10 nM GLP-I at 2.8 mM glucose (67%). Somatostatin secretion was increased by 10 mM glucose (2.8 mM glucose, 100%; 10 mM glucose, 166%). GLP-I stimulated somatostatin release in the presence of 2.8 mM glucose (172%). Pancreatic polypeptide (PP) secretion was enhanced by 10 mM glucose (2.8 mM glucose, 100%; 10 mM glucose, 236%), GLP-I induced PP release only in the presence of 2.8 mM glucose (184%).
引用
收藏
页码:196 / 200
页数:5
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