Shepherd-Rose A J, Pendleton R G
Eur J Pharmacol. 1984 Oct 1;105(1-2):57-63. doi: 10.1016/0014-2999(84)90648-4.
The H2-receptor blocking properties of L-643,441 were compared with ranitidine in isolated rabbit gastric glands. [14C]Aminopyrine uptake was used as the indicator of gastric acid secretion. Unlike ranitidine, inhibition by L-643,441 was time-dependent, only partially reversible, and was not surmounted by increasing doses of histamine. These and other findings are similar to those found previously in guinea pig atria, providing further evidence that at the receptor level, the mechanism of action of L-643, 441 is different from standard H2-receptor antagonists such as ranitidine.
在分离的兔胃腺中,比较了L-643,441与雷尼替丁的H2受体阻断特性。使用[14C]氨基比林摄取作为胃酸分泌的指标。与雷尼替丁不同,L-643,441的抑制作用是时间依赖性的,仅部分可逆,并且不会因组胺剂量增加而被克服。这些以及其他发现与先前在豚鼠心房中发现的结果相似,进一步证明在受体水平上,L-643,441的作用机制与雷尼替丁等标准H2受体拮抗剂不同。