GALANIN-INDUCED INHIBITION OF INSULIN-SECRETION FROM RAT ISLETS - EFFECTS OF RAT AND PIG GALANIN AND GALANIN FRAGMENTS AND ANALOGS

被引:24
作者
GREGERSEN, S
HERMANSEN, K
LANGEL, U
FISONE, G
BARTFAI, T
AHREN, B
机构
[1] HORSENS HOSP,DEPT MED,HORSENS,DENMARK
[2] UNIV STOCKHOLM,ARRHENIUS LAB,DEPT BIOCHEM,S-10691 STOCKHOLM,SWEDEN
[3] UNIV LUND,DEPT PHARMACOL,S-22101 LUND,SWEDEN
关键词
GALANIN; PANCREATIC ISLETS; INSULIN SECRETION;
D O I
10.1016/0014-2999(91)90797-T
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 29-amino acid neuropeptide galanin occurs in intrapancreatic nerves and inhibits insulin secretion. To study the structure-activity relations of galanin, we examined the effects of pig and rat galanin, three galanin fragments (galanin-(1-11), galanin-(1-16) and rat galanin-(17-29) and four galanin analogues ([Ala2]pig galanin, [Ala2]rat galanin, [D-Trp2]rat galanin and [D-Trp2]galanin-(1-16)) on glucose-stimulated insulin secretion from isolated rat islets. Pig and rat galanin and galanin-(1-11) equipotently inhibited glucose-stimulated (8.3 mM) insulin secretion at and above 10(-7) M (P < 0.05), whereas galanin-(1-16), inhibited insulin secretion at 10(-6) M (P < 0.01). In contrast, the C-terminal rat galanin-(17-29) and the galanin analogues did not influence insulin secretion. Thus, rat and pig galanin are equipotent in inhibiting glucose-stimulated insulin secretion from rat islets. The active site resides in the N-terminal part of the molecule. Furthermore, the binding of galanin to its receptor depends on structural characteristics governed by the N-terminal position and in particular by the Trp2 residue.
引用
收藏
页码:111 / 114
页数:4
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