Gastrin-releasing peptide stimulates possum gallbladder contractility in vitro

被引:7
作者
Carbone, A [1 ]
Schloithe, AC [1 ]
Harvey, JR [1 ]
Baker, RA [1 ]
Saccone, GTP [1 ]
机构
[1] FLINDERS MED CTR,DEPT SURG,BEDFORD PK,SA 5042,AUSTRALIA
基金
英国医学研究理事会;
关键词
gallbladder; contractility; neuropeptide; pharmacology;
D O I
10.1016/S0196-9781(97)00034-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reports of the action of gastrin-releasing peptide (GRP) on gallbladder contraction are limited to a few species. We compared the action of GRP, acetyl gastrin-releasing peptide 20-27 (GRP 20-27), and cholecystokinin-octapeptide (CCK-8) on gallbladder contractility with and without pretreatment with the neural inhibitor tetrodotoxin (TTX) and the bombesin antagonist [D-Phr 6, Des-Met 14]-bombesin 6-14 ethylamide (BBS 6-14 E). Full-thickness muscle strips were prepared and suspended in organ baths. The maximum GRP, GRP 20-27, and CCK-8 responses were 54.2 +/- 4.2%, 74.6 +/- 6.4%. and 69.3 +/- 6.9% of that of carbachol, respectively. Pretreatment with TTX influenced the action of GRP 20-27, and pretreatment with BBS 6-14 E influenced that of GRP and GRP 20-27. These studies show that GRP and GRP 20-27 are potent agonists of gallbladder contractility, acting via GRP-preferring receptors, and that GRP 20-27 also acts via a neural component. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:1067 / 1071
页数:5
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