Novel approaches to the pharmacological blockade of gastric acid secretion

被引:61
|
作者
Parsons, ME [1 ]
Keeling, DJ
机构
[1] Univ Hertfordshire, Dept Biosci, Hatfield AL10 9AB, Herts, England
[2] AstraZeneca R&D Charnwood, Lead Generat Biol Mol Biol, Loughborough LE11 5RH, Leics, England
关键词
gastrin receptor antagonists; GORD; H+/K+-ATPase; H-3 receptor agonists; potassium-competitive acid blocker;
D O I
10.1517/13543784.14.4.411
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Research into new methods of controlling acid secretion is driven by existing medical needs in gastro-oesophageal reflux disease treatment. Histamine receptor subtype 3 agonists offer one approach for acid inhibition but no agent is yet undergoing clinical testing. Other, as yet unrealised strategies include preventing the fusion of the tubulovesicular elements that contain H+/K+-ATPase with the parietal cell membrane, or blocking channels that recycle K+ in the parietal cell. Of more promise are gastrin (cholecystokinin) receptor antagonists and potassium-competitive acid blockers; examples of both are in clinical development. It is probable that gastrin receptor antagonists would be used adjunctively with proton pump inhibitors, possibly for meal-induced reflux. The potassium-competitive acid blockers have attributes that may facilitate use as monotherapy for the treatment of gastro-oesophageal reflux disease. The early promise of gastrin receptor antagonists and potassium-competitive acid blockers remains to be defined in large-scale trials.
引用
收藏
页码:411 / 421
页数:11
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