Abstract
ALE-36, as well as omeprazole and SCH 28080, markedly inhibited the [l4C]aminopyrine (AP) accumulation induced by dibutyryl cyclic AMP (dbcAMP) and H+, K+-ATPase activity in a concentration-dependent manner. The inhibitory effect of omeprazole on the dbcAMP-induced [14C]AP accumulation was reversed by treatment with β-mercaptoethanol, but those of ALE-36 and SCH 28080 were not. ALE-36 and SCH 28080 did not inhibit dog renal Na+, K+-ATPase activity, while omeprazole and ouabain did inhibit this enzyme activity. These results suggest that the inhibitory action of ALE-36 on acid secretion is due to the specific inhibition of gastric H+, K+-ATPase, the manner being different from in the case of omeprazole.