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[新型抗溃疡药物雷米诺拉唑对大鼠胃黏膜H⁺,K⁺-ATP酶活性的影响]

[Effect of a new antiulcer drug, leminoprazole, on the gastric mucosal H+,K(+)-ATPase activity in rats].

作者信息

Matsukura H, Masuda M, Uchida A, Kamishiro T

机构信息

Research Laboratories, Nippon Chemiphar Co., Ltd., Saitama, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1994 Aug;104(2):91-100. doi: 10.1254/fpj.104.91.

Abstract

The inhibitory action of leminoprazole on the activity of rat gastric mucosal H+,K(+)-ATPase was investigated in vitro and ex vivo. Leminoprazole and omeprazole concentration-dependently inhibited the H+,K(+)-ATPase activity, and their IC50 values were 31 microM and 24 microM, respectively, at pH7.4. Leminoprazole dose-dependently inhibited the H+,K(+)-ATPase activity at 3 and 6 hr after the administration at 10-100 mg/kg, p.o. Leminoprazole (60 mg/kg, p.o.) inhibited the H+,K(+)-ATPase activity persistently, and the duration of its inhibitory action was much longer than that of omeprazole (30 mg/kg, p.o.). In pylorus-ligated rats, good correlations between the respective inhibitory rates against gastric acid output and H+,K(+)-ATPase activity was found after the administration of leminoprazole. These results suggest that leminoprazole inhibits the gastric acid secretion by its ability to inhibit the H+,K(+)-ATPase activity in rats; its inhibitory activity was comparable to that of omeprazole. In addition, leminoprazole (100 mg/kg) inhibited the H+,K(+)-ATPase activity even when administered intragastrically after pylorus-ligation, suggesting that this drug can inhibit H+,K(+)-ATPase activity directly from the gastric lumen. Moreover, leminoprazole (100 mg/kg, p.o.) when administered repeatedly for 2 or 4 weeks inhibited the H+,K(+)-ATPase activity to the same degree as the single administration.

摘要

在体外和体内研究了雷米拉唑对大鼠胃黏膜H⁺,K⁺-ATP酶活性的抑制作用。雷米拉唑和奥美拉唑对H⁺,K⁺-ATP酶活性的抑制呈浓度依赖性,在pH7.4时,它们的半数抑制浓度(IC50)值分别为31微摩尔和24微摩尔。口服给予雷米拉唑10 - 100毫克/千克后3小时和6小时,其对H⁺,K⁺-ATP酶活性的抑制呈剂量依赖性。雷米拉唑(60毫克/千克,口服)持续抑制H⁺,K⁺-ATP酶活性,其抑制作用持续时间比奥美拉唑(30毫克/千克,口服)长得多。在幽门结扎的大鼠中,给予雷米拉唑后,发现其对胃酸分泌的抑制率与H⁺,K⁺-ATP酶活性之间有良好的相关性。这些结果表明,雷米拉唑通过抑制大鼠胃黏膜H⁺,K⁺-ATP酶活性来抑制胃酸分泌;其抑制活性与奥美拉唑相当。此外,即使在幽门结扎后经胃内给药,雷米拉唑(100毫克/千克)仍能抑制H⁺,K⁺-ATP酶活性,这表明该药物可直接从胃腔抑制H⁺,K⁺-ATP酶活性。而且,雷米拉唑(100毫克/千克,口服)连续重复给药2周或4周时,对H⁺,K⁺-ATP酶活性的抑制程度与单次给药相同。

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