Durcan M J, Lister R G
Laboratory of Clinical Studies, NIAAA, Bethesda, MD 20892.
Pharmacol Biochem Behav. 1989 Mar;32(3):667-70. doi: 10.1016/0091-3057(89)90015-4.
The ability of the benzodiazepine receptor partial inverse agonists Ro 15-4513, Ro 15-3505 and FG 7142, and the picrotoxin site ligands pentylenetetrazole and Ro 5-3663 to reduce ethanol-induced intoxication were investigated. Ro 15-4513 (0.3-3 mg/kg), Ro 15-3505 (3 mg/kg), pentylenetetrazole (20 and 25 mg/kg) and Ro 5-3663 (4 mg/kg) all significantly attenuated the intoxicating effects of ethanol. In contrast, FG 7142 (20 and 40 mg/kg) failed to reduce ethanol intoxication, but reversed the effect of Ro 15-4513. This pattern of results differs from that obtained using other behavioral paradigms. Since drugs which reduce the effects of GABA generally reduce the intoxicating effects of ethanol, it is suggested that the beta-carbolines may be unusual in their interaction with ethanol.
研究了苯二氮䓬受体部分反向激动剂Ro 15-4513、Ro 15-3505和FG 7142,以及印防己毒素位点配体戊四氮和Ro 5-3663减轻乙醇诱导的中毒的能力。Ro 15-4513(0.3 - 3毫克/千克)、Ro 15-3505(3毫克/千克)、戊四氮(20和25毫克/千克)和Ro 5-3663(4毫克/千克)均显著减弱了乙醇的中毒作用。相比之下,FG 7142(20和40毫克/千克)未能减轻乙醇中毒,但逆转了Ro 15-4513的作用。这种结果模式与使用其他行为范式所获得的结果不同。由于一般来说,降低GABA作用的药物会减轻乙醇的中毒作用,因此有人提出β-咔啉与乙醇的相互作用可能不同寻常。