Lippa A S, Coupet J, Greenblatt E N, Klepner C A, Beer B
Pharmacol Biochem Behav. 1979 Jul;11(1):99-106. doi: 10.1016/0091-3057(79)90304-6.
CL 218,872 is the first non-benzodiazepine to selectively displace brain specific 3H-diazepam binding with a potency comparable to that of the benzodiazepines. Like the benzodiazepines, CL 218,872 increased punished responding in a conflict situation and protected against the convulsions induced by pentylenetetrazole. These three pharmacological properties are highly predictive of anxiolytic activity. Unlike the benzodiazepines, however, CL 218,872 was relatively inactive in tests designed to measure effects on neuronal systems which utilize GABA, glycine and serotonin as transmitters. Furthmore, CL 218,872 was relatively free of the ataxic and depressant side effects commonly associated with the benzodiazepines. Because of this high degree of selectivity, CL 218,872 may represent a new probe for investigating neuronal substrates of anxiety.
CL 218,872是首个能选择性取代脑特异性3H-地西泮结合位点的非苯二氮䓬类药物,其效力与苯二氮䓬类药物相当。与苯二氮䓬类药物一样,CL 218,872在冲突情境中增加了受罚反应,并预防了戊四氮诱发的惊厥。这三种药理特性高度预示着抗焦虑活性。然而,与苯二氮䓬类药物不同的是,CL 218,872在旨在测量对利用γ-氨基丁酸、甘氨酸和5-羟色胺作为递质的神经元系统影响的试验中相对无活性。此外,CL 218,872相对没有通常与苯二氮䓬类药物相关的共济失调和抑制性副作用。由于这种高度的选择性,CL 218,872可能代表一种用于研究焦虑神经元底物的新探针。