Simon B, Kather H
Pharmacology. 1979;19(2):96-103. doi: 10.1159/000137294.
The effects of various nonsteroid anti-inflammatory compounds on human gastric mucosal adenylate cyclase were tested. It is shown that fenamates, indomethacin and diclofenac-Na were relatively specific inhibitors of prostaglandin E2 action at the level of the mucosal cyclase activity. The results suggest that inhibition of prostaglandin E2-activated adenylate cyclase might at least in part contribute to the ulcerogenic effects of certain nonsteroid anti-inflammatory drugs.
测试了各种非甾体抗炎化合物对人胃黏膜腺苷酸环化酶的作用。结果表明,灭酸类、吲哚美辛和双氯芬酸钠在黏膜环化酶活性水平上是前列腺素E2作用的相对特异性抑制剂。结果提示,抑制前列腺素E2激活的腺苷酸环化酶可能至少部分地导致某些非甾体抗炎药的致溃疡作用。