Nakane T, Chiba S
Eur J Pharmacol. 1986 Dec 16;132(2-3):327-31. doi: 10.1016/0014-2999(86)90626-6.
The mechanism of clonidine-induced vasodilatation was investigated in the isolated and perfused canine coronary arteries. Clonidine produced a slight vasoconstriction at small doses whereas it induced a dose-related vasodilatation at large doses (more than 3 micrograms). The vasodilatation was reversed to vasoconstriction by treatment with 100 micrograms of cimetidine (a selective H2-receptor antagonist) but was not affected by 100 micrograms of chlorpheniramine (a selective H1-receptor antagonist). These results suggest that clonidine can dilate the isolated and perfused canine coronary arteries by acting on histamine H2-receptors.
在离体灌注的犬冠状动脉中研究了可乐定诱导血管舒张的机制。小剂量可乐定产生轻微血管收缩,而大剂量(超过3微克)时则诱导剂量相关的血管舒张。用100微克西咪替丁(一种选择性H2受体拮抗剂)处理可使血管舒张逆转为血管收缩,但100微克氯苯那敏(一种选择性H1受体拮抗剂)对其无影响。这些结果表明,可乐定可通过作用于组胺H2受体使离体灌注的犬冠状动脉舒张。