Determinants of the short-term gastric damage caused by NSAIDs in man

被引:65
作者
Bjarnason, I.
Scarpignato, C.
Takeuchi, K.
Rainsford, K. D.
机构
[1] Guys Kings St Thomas Med Sch, Dept Med, London SE5 9PJ, England
[2] Maggiore Univ Hosp, Lab Clin Pharmacol, Parma, Italy
[3] Sheffield Hallam Univ, Biomed Res Ctr, Sheffield S1 1WB, S Yorkshire, England
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ANTI-INFLAMMATORY DRUGS; PLACEBO-CONTROLLED TRIAL; PEPTIC-ULCER DISEASE; MITOCHONDRIAL OXIDATIVE-PHOSPHORYLATION; SERIOUS GASTROINTESTINAL COMPLICATIONS; HELICOBACTER-PYLORI INFECTION; GASTRODUODENAL MUCOSAL DAMAGE; RANDOMIZED CONTROLLED-TRIAL; CYCLOOXYGENASE; INHIBITOR;
D O I
10.1111/j.1365-2036.2007.03348.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The short-term gastric damage seen with non-steroidal anti-inflammatory drugs (NSAIDs) in man may involve inhibition of cyclooxygenase (COX-1) and COX-2 as well as the topical irritancy, which is dependant on the acidity (pKa) and/or lipophilicity (log P-7.4). Aim To study the quantitative relationship between NSAID-induced short-term gastric damage, their physicochemical properties and contrasting roles of COX-1 and COX-2 inhibition. Methods We identified studies that allowed a qualitative comparison of the gastric injury (Lanza scores) induced by NSAIDs with their pKa and log P-7.4. Damage was correlated with gastric COX inhibition and potency to inhibit COX-1 and 2 and their COX-2/COX-1 selectivity ratio. Results The gastric damage correlates significantly with pKa (r = -0.69; P < 0.01), log P (r = -0.58, P < 0.05) and potency of the NSAIDs to inhibit COX-1 (r = -0.61, P < 0.02), but not with COX-2 inhibition or COX-2/COX-1 selectivity. Conclusions Against a background of COX-1 and COX-2 inhibition, the physicochemical properties of NSAID appear to play an important role in short-term gastric damage.
引用
收藏
页码:95 / 106
页数:12
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