File S E, Pellow S
Psychopharmacology (Berl). 1983;80(2):166-70. doi: 10.1007/BF00427962.
RO5-4864, a ligand for both the peripheral and for the central nervous system micromolar benzodiazepine binding sites, was investigated in the holeboard, alone and in combination with several other drugs. RO5-4864 alone caused a marked reduction in rears and motor activity and reduced head-dipping when objects were placed under the holes. All these reductions were enhanced by picrotoxin (2 and 4 mg/kg) and by CGS 8216 (3 mg/kg). RO15-1788 (10 mg/kg) reversed the reduction in rears and PK11195 (30 mg/kg), a putative antagonist for the peripheral binding site, reversed the reduction in head-dipping. The results are discussed in terms of the various benzodiazepine binding sites and possible non-specific drug effects.
RO5 - 4864是一种作用于外周和中枢神经系统微摩尔苯二氮䓬结合位点的配体,在洞板实验中,单独使用以及与其他几种药物联合使用时,对其进行了研究。单独使用RO5 - 4864会导致动物竖毛和运动活动显著减少,并且当在洞下放置物体时,会减少探首次数。所有这些减少现象会被印防己毒素(2和4毫克/千克)以及CGS 8216(3毫克/千克)增强。RO15 - 1788(10毫克/千克)可逆转竖毛减少现象,而PK11195(30毫克/千克),一种外周结合位点的假定拮抗剂,可逆转探首次数的减少。将根据各种苯二氮䓬结合位点以及可能的非特异性药物作用来讨论这些结果。