Gastric gland degeneration induced in monkeys by the CCK-B/gastrin receptor antagonist CI-988

被引:7
作者
Dethloff, LA
Robertson, DG
Tierney, BM
Breider, MA
Bestervelt, LL
机构
[1] Dept. of Pathol. and Exp. Toxicology, Parke-Davis Pharmaceutical Research, Warner-Lambert Company, Ann Arbor, MI 48105
关键词
cholecystokinin (CCK); gastrin; PD; 134308;
D O I
10.1177/019262339702500502
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastric effects of subchronic treatment with the cholecystokinin-B (CCK-B)/gastrin receptor antagonist CI-988 were investigated in cynomolgus monkeys. In preliminary range-finding studies, CI-988 was given orally to 1 monkey per sex for 14 days at doses of 50, 100, 200, and 500 mg/kg/day. Subchronic studies of CI-988 were subsequently conducted using 5 monkeys per sex at doses of 0, 5, 25, and 75 mg/kg for 4 or 13 wk. High-dose monkeys were dosed initially at 100 mg/kg, but the dose was not well tolerated and was decreased to 75 mg/kg after 8 days of treatment. One male monkey at 75 mg/kg was euthanatized in estremis on day 23. In the range-finding study, minimal to moderate, multifocal to diffuse degeneration of gastric glands, primarily in the fundic region, was observed at 100 mg/kg and above, with frank gastric mucosal atrophy occurring at 200 and 500 mg/kg. Minimal to mild gastric gland degeneration was also observed in the subchronic study after 4 wk at 25 and 75 mg/kg, but histopathologic gastric changes were remarkably absent after 13 wk. Mucosal height in the stomach fundus was decreased 19.8% in 75-mg/kg males at week 4, and although gastric mucosa appeared histologically normal after 13 wk, mucosal height remained 28.6% less than that of controls. In females at 75 mg/kg, fundic mucosal height was decreased 7% and 5% at weeks and 13, respectively, but decreases were not statistically significant. Mean serum gastrin concentrations were increased 10-fold in males only after 4 wk at 75 mg/kg, but were comparable to controls during week 13. CI-988-induced gastric gland degeneration is consistent with antagonism of gastrin's trophic activity toward gastric mucosa. Notwithstanding decrements in gastric mucosal height, disappearance of mild histopathologic findings despite continued treatment with the ligand suggests some degree of adaptation to subchronic CCK-B/gastrin inhibition, although the mechanism of accomodation has yet to be delineated.
引用
收藏
页码:441 / 448
页数:8
相关论文
共 56 条
[1]   GASTRIC ECL-CELL HYPERPLASIA AND CARCINOIDS IN RODENTS FOLLOWING CHRONIC ADMINISTRATION OF H2-ANTAGONISTS SK-AND-F-93479 AND OXMETIDINE AND OMEPRAZOLE [J].
BETTON, GR ;
DORMER, CS ;
WELLS, T ;
PERT, P ;
PRICE, CA ;
BUCKLEY, P .
TOXICOLOGIC PATHOLOGY, 1988, 16 (02) :288-298
[2]  
BLEVINS GT, 1994, J PHARMACOL EXP THER, V269, P911
[3]   TROPHIC EFFECT OF GASTRIN ON THE ENTEROCHROMAFFIN LIKE CELLS OF THE RAT STOMACH - ESTABLISHMENT OF A DOSE-RESPONSE RELATIONSHIP [J].
BRENNA, E ;
WALDUM, HL .
GUT, 1992, 33 (10) :1303-1306
[4]   PHARMACOLOGICAL BASIS FOR THE INDUCTION OF GASTRIC CARCINOID-TUMORS IN THE RAT BY LOXTIDINE, AN UNSURMOUNTABLE HISTAMINE H-2-RECEPTOR BLOCKING DRUG [J].
BRITTAIN, RT ;
JACK, D ;
REEVES, JJ ;
STABLES, R .
BRITISH JOURNAL OF PHARMACOLOGY, 1985, 85 (04) :843-847
[5]   SOMATOSTATIN CELLS IN THE OXYNTIC MUCOSA OF HYPOGASTRINEMIC OR HYPERGASTRINEMIC RATS [J].
CHEN, D ;
URIBE, A ;
HAKANSON, R ;
SUNDLER, F .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1992, 27 (06) :479-482
[6]   BIOLOGICAL ACTIONS OF CHOLECYSTOKININ [J].
CRAWLEY, JN ;
CORWIN, RL .
PEPTIDES, 1994, 15 (04) :731-755
[7]   THE ACHLORHYDRIA-CARCINOID SEQUENCE - ROLE OF GASTRIN [J].
CREUTZFELDT, W .
DIGESTION, 1988, 39 (02) :61-79
[8]  
DETHLOFF L, FOOD CHEM TOXICOL
[9]  
DETHLOFF L, 1995, TOXICOLOGIST, V16, pA1708
[10]   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