Kaminka M E, Tupikina S M, Mashkovskiĭ M D
Biull Eksp Biol Med. 1983 May;95(5):44-6.
Experiments were made to study the influence of a new antihistaminic drug phencarol [(quinuclidyl-3) diphenylcarbinol hydrochloride] on gastric secretion in rats. Unlike the blockers of H1-histamine receptors (diphenhydramine, omeril, pyrilamine, and cyproheptadine), phencarol reduces secretion and the content of free hydrochloric acid in the gastric contents. The antacid activity of the drug is similar to that of the H2-receptor blocker, cimetidine. However, phencarol differs from the latter drug in the mechanism of action. The antacid action of phencarol is likely to be the result of its activation effect on diamine oxidase, which leads to a decrease in the content of active histamine in the tissues and diminution of its supply to H2-histamine receptors that control gastric secretion.
进行了实验以研究一种新型抗组胺药物苯卡洛尔[(奎宁环基-3)二苯基甲醇盐酸盐]对大鼠胃分泌的影响。与H1组胺受体阻滞剂(苯海拉明、奥米立、吡苄明和赛庚啶)不同,苯卡洛尔可减少胃内容物的分泌及游离盐酸含量。该药物的抗酸活性与H2受体阻滞剂西咪替丁相似。然而,苯卡洛尔在作用机制上与后一种药物不同。苯卡洛尔的抗酸作用可能是其对二胺氧化酶的激活作用的结果,这导致组织中活性组胺含量降低,并减少其向控制胃分泌的H2组胺受体的供应。