Charveron M, Assié M B, Stenger A, Briley M
Eur J Pharmacol. 1984 Nov 13;106(2):313-7. doi: 10.1016/0014-2999(84)90718-0.
Raubasine produced a dose-related inhibition of specific [3H]flunitrazepam binding to rat brain membranes. Scatchard analyses revealed a significant increase in the affinity constant but no change in the number of binding sites, suggesting that raubasine acts as a competitive inhibitor. Raubasine also inhibited the in vivo binding of [3H]flunitrazepam to mouse brain sites. Behavioral studies showed raubasine to possess anticonvulsant properties against pentylenetetrazol- and bicuculline-induced convulsions in mice. These effects were inhibited by the benzodiazepine antagonist, Ro 15-1788. The results suggest that raubasine interacts directly at benzodiazepine sites with a benzodiazepine agonist-type activity.
萝巴新对大鼠脑膜中特异性[3H]氟硝西泮结合产生剂量相关的抑制作用。Scatchard分析显示亲和常数显著增加,但结合位点数量无变化,提示萝巴新作为竞争性抑制剂发挥作用。萝巴新还抑制了[3H]氟硝西泮在小鼠脑部位的体内结合。行为学研究表明,萝巴新对小鼠戊四氮和荷包牡丹碱诱导的惊厥具有抗惊厥特性。这些作用被苯二氮䓬拮抗剂Ro 15 - 1788抑制。结果表明,萝巴新在苯二氮䓬位点直接相互作用,具有苯二氮䓬激动剂样活性。