Plunkett L M, Tackett R L
J Pharm Pharmacol. 1987 Jan;39(1):29-34. doi: 10.1111/j.2042-7158.1987.tb07157.x.
The role of the dopaminergic system in digoxin-induced cardiotoxicity has been examined. Specific dopaminergic agonists and antagonists were administered into the ventriculocisternal system of pentobarbitone-anaesthetized dogs before systemic administration of digoxin. Pretreatment with apomorphine, a specific dopamine agonist, did not significantly alter the arrhythmogenic or lethal doses of digoxin. However, the digoxin-induce increase in CSF noradrenaline was decreased significantly in apomorphine-pretreated animals. Pretreatment with pimozide, a specific dopamine antagonist, significantly decreased the arrhythmogenic dose of digoxin but did not alter the lethal dose. As with apomorphine, pimozide-pretreated animals accumulated significantly less noradrenaline in CSF compared with control dogs. These results suggest that dopamine receptors are not directly related to the cardiotoxic actions of digoxin. However, dopaminergic receptors may influence the balance of central catecholaminergic systems that influence the peripheral cardiovascular system.
已对多巴胺能系统在洋地黄毒苷诱发心脏毒性中的作用进行了研究。在对戊巴比妥麻醉的犬全身给予洋地黄毒苷之前,将特定的多巴胺能激动剂和拮抗剂注入脑室池系统。用特定的多巴胺激动剂阿扑吗啡预处理,并未显著改变洋地黄毒苷的致心律失常剂量或致死剂量。然而,在阿扑吗啡预处理的动物中,洋地黄毒苷诱导的脑脊液去甲肾上腺素增加显著降低。用特定的多巴胺拮抗剂匹莫齐特预处理,显著降低了洋地黄毒苷的致心律失常剂量,但未改变致死剂量。与阿扑吗啡一样,与对照犬相比,匹莫齐特预处理的动物脑脊液中去甲肾上腺素的蓄积量显著减少。这些结果表明,多巴胺受体与洋地黄毒苷的心脏毒性作用无直接关系。然而,多巴胺能受体可能会影响中枢儿茶酚胺能系统的平衡,而该系统会影响外周心血管系统。