OMEPRAZOLE - INHIBITOR OF BOTH ACID FORMATION AND TRANSLOCATION IN GASTRIC-MUCOSA

被引：6

作者：

EKBLAD, EBM

机构：

来源：

ACTA PHYSIOLOGICA SCANDINAVICA | 1989年 / 137卷 / 02期

关键词：

D O I：

10.1111/j.1748-1716.1989.tb08742.x

中图分类号：

Q4 [生理学];

学科分类号：

071003 ;

摘要：

引用

收藏

页码：223 / 230

页数：8

相关论文

共 12 条

[1] THE SULFOXIDE MOIETY OF SUBSTITUTED BENZIMIDAZOLES IS ESSENTIAL FOR INHIBITION OF PARIETAL-CELL K+/H+-ATPASE
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[2] THIOCYANATE AND NITRITE INHIBIT PROTON TRANSLOCATION IN GASTRIC MUSOSA
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[3] CONSERVATIVE AND NONCONSERVATIVE INHIBITORS OF GASTRIC-ACID SECRETION
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[4] INVARIANT RELATION BETWEEN TOTAL ACID-SECRETION AND SECRETAGOGUE EXPOSURE - SECRETORY DYNAMICS IN BULLFROG
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[5] SUBSTITUTED BENZIMIDAZOLES INHIBIT GASTRIC-ACID SECRETION BY BLOCKING (H++K+)ATPASE
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[6] INHIBITION OF ACID-SECRETION IN ISOLATED GASTRIC GLANDS BY SUBSTITUTED BENZIMIDAZOLES
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[J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 243 (06): : G505 - G510
[7] DISSOCIATED RESPONSE OF ACID AND PEPSIN-SECRETION TO OMEPRAZOLE IN AN INVITRO PERFUSED MOUSE STOMACH
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[8] FRYKLUND J, 1986, J PHARMACOL EXP THER, V236, P248
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[10] INHIBITION OF (H++K+)-ATPASE BY OMEPRAZOLE IN ISOLATED GASTRIC VESICLES REQUIRES PROTON TRANSPORT
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