Pharmacological control of gastric acid secretion for the treatment of acid-related peptic disease: past, present, and future

被引:64
作者
Aihara, T [1 ]
Nakamura, E [1 ]
Amagase, K [1 ]
Tomita, K [1 ]
Fujishita, T [1 ]
Furutani, K [1 ]
Okabe, S [1 ]
机构
[1] Kyoto Pharmaceut Univ, Dept Appl Pharmacol, Kyoto 6078414, Japan
关键词
gastric acid secretion; ulcer disease; H-2; receptor; M-3; gastrin/CCK2; histidine decarboxylase;
D O I
10.1016/S0163-7258(03)00015-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacological agents, such as histamine H-2 receptor antagonists and acid pump inhibitors, are now the most frequently used treatment for such acid-related diseases as gastroduodenal ulcers and reflux esophagitis. Based on increased understanding of the precise mechanisms of gastric acid secretion at the level of receptors, enzymes, and cytoplasmic signal transduction systems, further possibilities exist for the development of effective antisecretory pharmacotherapy. Gastrin CCK2 receptor antagonists and locally active agents appear to represent promising therapies for the future. Development of gene targeting techniques has allowed production of genetically engineered transgenic and knockout mice. Such genetic technology has increased the investigative power for pharmacotherapy for not only antisecretory agents, but also treatment of mucosal diseases, such as atrophy, hyperplasia, and cancer. Elucidation of the origin of gastric parietal cells also represents an interesting investigative target that should allow a better understanding of not only acid-related diseases, but also the evolution of the stomach as an acid-secreting organ. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:109 / 127
页数:19
相关论文
共 114 条
[1]  
Aihara T, 2002, GASTROENTEROLOGY, V122, pA252
[2]   Antisecretory and ulcer healing effects of S-0509, a novel CCK-B gastrin receptor antagonist, in rats [J].
Amagase, K ;
Ikeda, K ;
Okabe, S .
DIGESTIVE DISEASES AND SCIENCES, 1999, 44 (05) :879-888
[3]   DEFINITION AND ANTAGONISM OF HISTAMINE H2-RECEPTORS [J].
BLACK, JW ;
PARSONS, EM ;
DURANT, CJ ;
DUNCAN, WAM ;
GANELLIN, CR .
NATURE, 1972, 236 (5347) :385-&
[4]   The very small-conductance K+ channel KVLQT1 and epithelial function [J].
Bleich, M ;
Warth, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2000, 440 (02) :202-206
[5]   K(v)LQT channels are inhibited by the K+ channel blocker 293B* [J].
Bleich, M ;
Briel, M ;
Busch, AE ;
Lang, HJ ;
Gerlach, U ;
Gogelein, H ;
Greger, R ;
Kunzelmann, K .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1997, 434 (04) :499-501
[6]   THE EFFECT OF SODIUM FLUORIDE ON THE OUTPUT OF SOME ELECTROLYTES FROM THE GASTRIC MUCOSA OF CATS [J].
BOND, AM ;
HUNT, JN .
JOURNAL OF PHYSIOLOGY-LONDON, 1956, 133 (02) :317-329
[7]   CIMETIDINE - NON-THIOUREA H2-RECEPTOR ANTAGONIST [J].
BRIMBLECOMBE, RW ;
DUNCAN, WAM ;
DURANT, GJ ;
EMMETT, JC ;
GANELLIN, CR ;
PARSONS, ME .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 1975, 3 (02) :86-92
[8]   INHIBITION OF GASTRIC-ACID SECRETION IN THE CONSCIOUS DOG BY THE MAST-CELL STABILIZING AGENT, FPL-52694 [J].
CANFIELD, SP ;
CURWAIN, BP .
BRITISH JOURNAL OF PHARMACOLOGY, 1983, 80 (01) :27-32
[9]   Genetic ablation of parietal cells in transgenic mice: A new model for analyzing cell lineage relationships in the gastric mucosa [J].
Canfield, V ;
West, AB ;
Goldenring, JR ;
Levenson, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (06) :2431-2435
[10]   GASTRIN AND GASTRIC ENTEROCHROMAFFIN-LIKE CELL CARCINOIDS IN THE RAT [J].
CARLSSON, E ;
HAVU, N ;
MATTSSON, H ;
EKMAN, L .
DIGESTION, 1990, 47 :17-23