Emerging drugs for gastroesophageal reflux disease

被引:10
作者
Boeckxstaens, G. E. [1 ,2 ]
机构
[1] Catholic Univ Louvain, Univ Hosp Leuven, Dept Gastroenterol, B-3000 Louvain, Belgium
[2] Univ Amsterdam, Acad Med Ctr, Dept Gastroenterol & Hepatol, NL-1105 AZ Amsterdam, Netherlands
关键词
GABA(B) agonist; gastroesophageal reflux disease; mGluR5; antagonist; potassium-competitive acid blockers; proton pump inhibitors; reflux inhibitors; LOWER ESOPHAGEAL SPHINCTER; PROTON-PUMP INHIBITOR; DELAYED-RELEASE FORMULATION; GABA(B) AGONIST BACLOFEN; HEALTHY-VOLUNTEERS; INTRAGASTRIC PH; EROSIVE ESOPHAGITIS; DEXLANSOPRAZOLE MR; CLINICAL-TRIALS; ACID REFLUX;
D O I
10.1517/14728210903133807
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proton pump inhibitors (PPIs) are very effective and safe drugs for the treatment of erosive and non-erosive gastroesophageal reflux disease (GERD). Nevertheless, a significant proportion of GERD patients (30 - 40%) continue to suffer from symptoms during PPI treatment, which has stimulated the search for better drugs. Improvement of PPI pharmacokinetics and pharmacodynamics has been the main focus of drug development in the past decade with the ultimate goal of optimizing acid inhibition. New inhibitors of the proton pump with a longer half-life, acting faster and longer, have been developed, including potassium-competitive acid blockers. Recent data, however, suggest that the therapeutic efficacy of acid suppression may have reached its maximum and other mechanisms may have to be targeted to further improve symptom control. Potential drugs interacting with different targets are reflux inhibitors such as GABA(B) receptor agonists; and mGluR5 antagonists. These agents reduce the number of transient lower esophageal sphincter relaxation thereby reducing both acid and non-acid reflux. Theoretically, visceral analgesics to modulate visceral perception or even growth factors to enhance mucosal healing may be other emerging drugs to treat GERD.
引用
收藏
页码:481 / 491
页数:11
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