Angus J A, Bobik A, Korner P I, Stoneham M T
Br J Pharmacol. 1978 Jan;62(1):7-17. doi: 10.1111/j.1476-5381.1978.tb07000.x.
1 The effects of guanethidine (0.5-4 mg/kg i.v.) on arterial pressure, hindlimb blood flow and hindlimb vascular resistance (HVR) were studied in unanesthetized rabbits subjected to "total" autonomic block. 2 Evidence that this response was mediated by histamine release was that (a) 3H-labelled histamine levels in the hindlimb venous blood rose substantially after guanethidine; (b) infusion of exogenous histamine caused an inhibition of the guanethidine-induced vasodilatation; and (c) competitive antagonism of the response was obtained with the H2-antagonist burimamide. 3 There was good correlation between the [3H]-histamine ;elease and the time course of the vasodilator response. Glyceryl trinitrate infusions that lowered HVR substantially, did not cause release of histamine. 4 Reserpine, desipramine and indomethacin pretreatment did not alter the vasodilator response to guanethidine. 5 The guanethidine vasodilator response was not influenced by the H1-antagonist mepyramine or by the other H2-antagonists, metiamide or cimetidine. The vascular receptors stimulated by endogenous histamine may be distinctive from those stimulated by exogenous histamine, or the action of guanethidine may involve greater production of histamine at an intracellular site that is more readily reached by burimamide than by the other H2-antagonists.
1 在接受“完全”自主神经阻断的未麻醉家兔中,研究了胍乙啶(静脉注射0.5 - 4毫克/千克)对动脉血压、后肢血流量和后肢血管阻力(HVR)的影响。2 表明这种反应是由组胺释放介导的证据如下:(a)胍乙啶给药后,后肢静脉血中3H标记的组胺水平大幅升高;(b)输注外源性组胺可抑制胍乙啶诱导的血管舒张;(c)用H2拮抗剂布立马胺可获得该反应的竞争性拮抗作用。3 [3H]组胺释放与血管舒张反应的时间进程之间存在良好的相关性。大幅降低HVR的硝酸甘油输注并未引起组胺释放。4 利血平、去甲丙咪嗪和吲哚美辛预处理并未改变对胍乙啶的血管舒张反应。5 胍乙啶的血管舒张反应不受H1拮抗剂美吡拉敏或其他H2拮抗剂甲硫咪胺或西咪替丁的影响。内源性组胺刺激的血管受体可能与外源性组胺刺激的不同,或者胍乙啶的作用可能涉及在细胞内位点产生更多组胺,布立马胺比其他H2拮抗剂更容易到达该位点。