Chugun A, Uchide T, Fujimori Y, Temma K, Hara Y, Sasaki T, Akera T
Department of Veterinary Pharmacology, School of Veterinary Medicine and Animal Sciences, Kitasato University, 35-1, Higashi 23-bancho, Aomori 034-8628, Towada, Japan.
Eur J Pharmacol. 2000 Oct 27;407(1-2):183-9. doi: 10.1016/s0014-2999(00)00729-9.
A hypotheses that mitoxantrone is a competitive antagonist at muscarinic cholinergic receptors was examined in guinea-pig hearts. In isolated left atrial muscle preparations, electrically paced at 2 Hz, the muscarinic agonist, carbachol, caused a concentration-dependent decrease in developed tension. Mitoxantrone caused a parallel right-ward shift of the concentration-response curve for carbachol. Schild plots for the effect of mitoxantrone on the carbachol concentration-response relationship were linear with a slope of 0.88 which was not significantly different from the unity. The right-ward shift of the carbachol concentration-response relationship by mitoxantrone significantly reversed after an additional incubation with a mitoxantrone-free solution, although the reversal was incomplete after a 2-h incubation in the mitoxantrone-free solution. Mitoxantrone caused a concentration-dependent displacement of specific [3H]quinuclidinyl benzilate binding to membrane preparations obtained from ventricular muscles of guinea-pig hearts. These results indicate that mitoxantrone acts as a competitive antagonist for the muscarinic receptors.
在豚鼠心脏中检验了米托蒽醌是毒蕈碱型胆碱能受体竞争性拮抗剂的假说。在以2 Hz频率进行电起搏的离体左心房肌制备物中,毒蕈碱激动剂卡巴胆碱引起张力产生的浓度依赖性降低。米托蒽醌使卡巴胆碱的浓度 - 反应曲线平行右移。米托蒽醌对卡巴胆碱浓度 - 反应关系影响的Schild图呈线性,斜率为0.88,与1无显著差异。用无米托蒽醌的溶液进一步孵育后,米托蒽醌引起的卡巴胆碱浓度 - 反应关系右移显著逆转,尽管在无米托蒽醌的溶液中孵育2小时后逆转不完全。米托蒽醌引起特异性[3H]喹核醇基苯甲酸酯与从豚鼠心脏心室肌获得的膜制备物结合的浓度依赖性位移。这些结果表明米托蒽醌作为毒蕈碱受体的竞争性拮抗剂起作用。