Tsai B S, Yellin T O
Biochem Pharmacol. 1984 Nov 15;33(22):3621-5. doi: 10.1016/0006-2952(84)90147-3.
The interaction of adenylate cyclase with histamine H2 receptor agents and with tricyclic antidepressants was studied in guinea pig gastric mucosal membranes. The H2 receptor antagonist tiotidine acted as a competitive inhibitor of histamine-stimulated adenylate cyclase. The tricyclic antidepressants imipramine and amitryptyline were also competitive inhibitors. The dissociation constant of imipramine was the same whether histamine or dimaprit was used to activate the enzyme. In membrane preparations that had been stored frozen, there was a marked increase in the concentration of histamine or dimaprit required to cause half-maximal enzyme stimulation, and the dissociation constants of some classical H2 receptor antagonists were greatly increased. In contrast, the dissociation constants of the antidepressants were either unchanged or decreased. These results suggest that antidepressants are potent blockers of H2 receptors in gastric mucosal membranes, but there are differences between antidepressants and classical H2 receptor antagonists in their interaction with H2 receptors.
在豚鼠胃黏膜膜中研究了腺苷酸环化酶与组胺H2受体激动剂以及三环类抗抑郁药的相互作用。H2受体拮抗剂替丁作为组胺刺激的腺苷酸环化酶的竞争性抑制剂。三环类抗抑郁药丙咪嗪和阿米替林也是竞争性抑制剂。无论使用组胺还是二甲双胍来激活酶,丙咪嗪的解离常数都是相同的。在冷冻保存的膜制剂中,引起酶刺激达到半数最大效应所需的组胺或二甲双胍浓度显著增加,一些经典H2受体拮抗剂的解离常数也大大增加。相比之下,抗抑郁药的解离常数要么不变,要么降低。这些结果表明,抗抑郁药是胃黏膜膜中H2受体的强效阻滞剂,但抗抑郁药与经典H2受体拮抗剂在与H2受体的相互作用上存在差异。