Studies on the Mechanism of Action of the Gastric H+, K+-ATPase Inhibitor SPI-447

The Japanese Journal of Pharmacology

Takashi Yamazaki¹  Mitsuhiro Narita¹  Kimiko Banno¹  Hironori Tanaka¹  Harumi Ishikawa¹  Toshihisa Ushiro¹  Jyoji Hirase¹  Toshiki Nishigaito¹  Toshio Ichihara¹  Yasuhiro Tsukimi¹ 

[1] Department of New Drug Research Laboratories,Technical Headquarters,Shinnippon Pharmaceutical,Inc.,370 Mita,Kishiwada 596-0808,Japan

关键词: H+;    K+-ATPase inhibitor;    Anti-ulcer drug;    SPI-447;    Omeprazole;    SCH28080;   

DOI  :  10.1254/jjp.82.21

学科分类：药理学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(28)Cited-By(5)3−Amino−5−methyl−2(2−methyl−3−thienyl)−imidazo[1, 2−a]thieno[3, 2−c]pyridine, SPI−447, is a potent gastric H+, K+−ATPase inhibitor, but a detailed mechanism of the inhibition is unknown.This study was designed to investigate the mechanism by which SPI−447 inhibits gastric H+, K+−ATPase.For this purpose, the inhibitory action of SPI−447 on gastric H+, K+−ATPase from porcine gastric mucosa was compared with that of omeprazole(an irreversible inhibitor)and SCH28080(a reversible inhibitor).All compounds produced dose−dependent inhibition of gastric H+, K+−ATPase, and the inhibitory intensities were increased under acidic conditions.The anti−H+, K+−ATPase actions of SPI−447 and SCH28080 were attenuated by dilution, but not influenced by glutathione pretreatment.In contrast, that of omeprazole was not influenced by dilution, but was suppressed by glutathione pretreatment.KCl addition reversed the inhibition of H+, K+−ATPase−mediated H+−transport by SPI−447 and SCH28080, but had no effect on that by omeprazole.The anti−gastric H+, K+−ATPase action of SPI−447 was additive with that of SCH28080.SPI−447 and SCH28080 had no effect on Na+, K+−ATPase activity.These findings indicated that the inhibitory mechanism of SPI−447 on gastric H+, K+−ATPase was similar to that of SCH28080, but different from that of omeprazole;i.e., 1)reversible, 2)SH−group independent, 3)K+−competitive, and 4)highly specific against gastric H+, K+−ATPase.

【 授权许可】

Unknown