YM022, a highly potent and selective CCKB antagonist inhibiting gastric acid secretion in the rat, the cat and isolated rabbit glands

被引:5
作者
Attoub, S [1 ]
Moizo, L [1 ]
Laigneau, JP [1 ]
Alchepo, B [1 ]
Lewin, MJM [1 ]
Bado, A [1 ]
机构
[1] Hop Bichat, INSERM, U10, IFR02 Cellules Epitheliales, F-75018 Paris 18, France
关键词
YM022; CCKB; gastrin receptor antagonist; acid secretion; isolated fundic glands; rat; cat; rabbit;
D O I
10.1111/j.1472-8206.1998.tb00952.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the effects of the novel CCKB/gastrin antagonist YM022 on gastric acid secretion in vivo and in vitro, compared to CI-988 and L365,260 as reference antagonists. In the anaesthetized raf pentagastrin-induced stimulation of gastric acid secretion was dose-dependently and up to 100% inhibited by iv administration of YM022 with an ID50 of 0.009 +/- 0.0006 mu mol/kg h in comparison to 0.6 +/- 0.03 and 3.40 +/- 0.05 mu mol/kg h for CI-988 and L-365,260, respectively, In the gastric fistula cat, iv administration of YM022 produced a similar inhibitory effect with an ID50 of 0.02 mu mol/kg in comparison to 1.6 and 2.5 mu mol/kg for CI-988 and L-365,260, respectively. Furthermore, bolus injection of 0.6 mu mol/kg YM022 produced 100% inhibition within 30 min and 85% inhibition was still observed after 3 h. In the isolated rabbit gastric glands, CCK8-stimulated C-14-aminopyrine uptake was inhibited according to the following rank order of potency: YM022 (IC50 = 0.0012 mu M) >> CI-988 (IC50 = 0.2 mu M) >> L365,260 (IC50 = 2.8 mu M). Unlike with L365,260, no influence of CI-988 and YM022 on histamine-stimulated acid output was shown in this study. Thus, YM022 is a highly potent and selective gastric CCKB/gastrin receptor antagonist and has a long-lasting inhibitory effect on gastric acid secretion. (C) 1998 Elsevier, Paris.
引用
收藏
页码:256 / 262
页数:7
相关论文
共 33 条
[1]   CHOLECYSTOKININ-A-RECEPTOR MEDIATION OF FOOD-INTAKE IN CATS [J].
BADO, A ;
DURIEUX, C ;
MOIZO, L ;
ROQUES, BP ;
LEWIN, MJM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :R693-R697
[2]   PHARMACOLOGICAL CHARACTERIZATION OF HISTAMINE H3-RECEPTORS IN ISOLATED RABBIT GASTRIC GLANDS [J].
BADO, A ;
MOIZO, L ;
LAIGNEAU, JP ;
LEWIN, MJM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (01) :G56-G61
[3]  
BLEVINS GT, 1994, J PHARMACOL EXP THER, V269, P911
[4]   BENZODIAZEPINE GASTRIN AND BRAIN CHOLECYSTOKININ RECEPTOR LIGANDS - L-365,260 [J].
BOCK, MG ;
DIPARDO, RM ;
EVANS, BE ;
RITTLE, KE ;
WHITTER, WL ;
VEBER, DF ;
ANDERSON, PS ;
FREIDINGER, RM .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (01) :13-16
[5]   CHOLECYSTOKININ-B RECEPTOR LIGANDS OF THE DIPEPTOID SERIES ACT AS AGONISTS ON RAT STOMACH HISTIDINE-DECARBOXYLASE [J].
DING, XQ ;
CHEN, D ;
HAKANSON, R .
GASTROENTEROLOGY, 1995, 109 (04) :1181-1187
[6]   EFFECT OF GASTRIN RECEPTOR ANTAGONISTS ON GASTRIC-ACID SECRETION AND GASTRIN AND SOMATOSTATIN RELEASE IN THE RAT STOMACH [J].
EISSELE, R ;
KOOP, H ;
BOTHESANDFORT, E ;
ARNOLD, R .
DIGESTION, 1992, 53 (3-4) :179-188
[7]  
HILL DR, 1987, J NEUROSCI, V7, P1967
[8]  
HIRST BH, 1991, ALIMENT PHARM THERAP, V5, P31
[9]   PD-135158, A CCK(B) GASTRIN RECEPTOR ANTAGONIST, STIMULATES RAT PANCREATIC-ENZYME SECRETION AS A CCK(A) RECEPTOR AGONIST [J].
HOCKER, M ;
HUGHES, J ;
FOLSCH, UR ;
SCHMIDT, WE .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 242 (01) :105-108
[10]   DEVELOPMENT OF CCK-B ANTAGONISTS [J].
HORWELL, DC .
NEUROPEPTIDES, 1991, 19 :57-64