Fisas M A, Gutiérrez B, Fort M, Dordal A, García C, Farré A J
Laboratorios Dr. Esteve, S.A., Barcelona, Spain.
Methods Find Exp Clin Pharmacol. 1998 Apr;20(3):199-210.
The general pharmacological profile and effects of E-4716 on the CNS have been investigated in comparison with other histamine receptor blockers. In in vitro studies with isolated organs and in binding studies on numerous receptors, E-4716 had no activity even at high concentrations, except for the selective blockade of H1 receptors. No activity was observed in pharmacological trials in vivo, such as the Irwin test or analgesia induced by phenylbenzoquinone or electroshock, suggesting a depressant activity on the CNS. In tests potentiating hypnosis induced by barbiturates, benzodiazepines and ethanol in mice, E-4716 always showed milder potentiating effects than the other reference drugs. In monkeys, no sedating effects were observed at 200 mg/kg, p.o. These results suggest that E-4716 exhibits good clinical efficacy without any secondary effects.
与其他组胺受体阻滞剂相比,已对E - 4716对中枢神经系统的一般药理学特征和作用进行了研究。在离体器官的体外研究以及对众多受体的结合研究中,E - 4716即使在高浓度下也无活性,但对H1受体有选择性阻断作用。在体内药理学试验中未观察到活性,如欧文试验或苯醌或电击诱导的镇痛试验,提示其对中枢神经系统有抑制活性。在增强小鼠巴比妥类、苯二氮䓬类和乙醇诱导的催眠作用的试验中,E - 4716的增强作用总是比其他参比药物更温和。在猴子中,口服200mg/kg未观察到镇静作用。这些结果表明,E - 4716具有良好的临床疗效且无任何副作用。