Hughes M J
J Clin Pharmacol. 1980 Jan;20(1):10-9. doi: 10.1002/j.1552-4604.1980.tb01661.x.
The histamine chronotropic response of rabbit atria appears to be controlled by both H1 and H2 receptors and can be blocked in part by either metiamide (an H2 antagonist) or diphenhydramine (an H1 antagonist), while both 2- and 4-methylhistamine (H1 and H2 agonists, respectively) stimulated the chronotropic response. At low agonist concentrations, the simultaneous presence of both H1 and H2 blockers results in considerably less inhibition than could be expected from calculations of individual inhibition data, suggesting that some sites behave as if they have both H1 and H2 properties. Additional compounds were tested for specific action on H1 and H2 receptors: 2-(2-pyridyl) ethylamine, reported to be an H1 agonist, appears to stimulate rabbit atria by releasing norepinephrine and guinea pig atria by releasing both norepinephrine and histamine; while dimaprit, reported to be an H2 agonist, may stimulate histamine receptors directly but has a nonspecific depressant action on rabbit atria which interferes with its use as an agonist in this species.
兔心房的组胺变时反应似乎受H1和H2受体两者控制,可被甲硫米特(一种H2拮抗剂)或苯海拉明(一种H1拮抗剂)部分阻断,而2-甲基组胺和4-甲基组胺(分别为H1和H2激动剂)均可刺激变时反应。在低激动剂浓度下,同时存在H1和H2阻滞剂时所产生的抑制作用,比根据单独抑制数据计算预期的要小得多,这表明某些位点的行为就好像它们同时具有H1和H2特性。还测试了其他化合物对H1和H2受体的特异性作用:据报道,2-(2-吡啶基)乙胺是一种H1激动剂,它似乎通过释放去甲肾上腺素来刺激兔心房,通过释放去甲肾上腺素和组胺来刺激豚鼠心房;而据报道,二甲双胍是一种H2激动剂,它可能直接刺激组胺受体,但对兔心房有非特异性抑制作用,这妨碍了它在该物种中用作激动剂。