Britton K T, Lee G, Koob G F
Department of Psychiatry, Veterans Administration Medical Center, La Jolla, CA 92161.
Psychopharmacology (Berl). 1988;94(3):306-11. doi: 10.1007/BF00174680.
The central nervous system stimulants corticotropin releasing factor (CRF) and amphetamine were administered in combination with the benzodiazepine ligands Ro 15-1788 and FG 7142 in order to assess their benzodiazepine agonist and antagonist receptor properties in an operant conflict test in rats. Ro 15-1788, which was without behavioral activity in this test when given alone, reversed the suppression of punished responding produced by CRF and amphetamine in a dose-dependent manner. Chlordiazepoxide, which produced a release of punished responding by itself, also reversed the suppression of punished responding produced by CRF but not that of amphetamine. The benzodiazepine inverse agonist FG 7142, in contrast, enhanced the rate suppressing actions of both CRF and amphetamine. In a locomotor activity test, Ro 15-1788 failed to block the locomotor activation observed with CRF and amphetamine. The results suggest that "anxiety" or stress-enhancing compounds may enhance the partial agonist properties of Ro 15-1788 in certain test situations.
为了在大鼠的操作性冲突试验中评估促肾上腺皮质激素释放因子(CRF)和苯丙胺这两种中枢神经系统兴奋剂与苯二氮䓬配体Ro 15 - 1788和FG 7142联合使用时的苯二氮䓬激动剂和拮抗剂受体特性。单独给予时在该试验中无行为活性的Ro 15 - 1788,以剂量依赖的方式逆转了CRF和苯丙胺对受罚反应的抑制作用。本身能使受罚反应释放的氯氮䓬,也逆转了CRF对受罚反应的抑制作用,但没有逆转苯丙胺的抑制作用。相比之下,苯二氮䓬反向激动剂FG 7142增强了CRF和苯丙胺对行为速率的抑制作用。在运动活动试验中,Ro 15 - 1788未能阻断CRF和苯丙胺所观察到的运动激活作用。结果表明,“焦虑”或应激增强化合物可能在某些试验情况下增强Ro 15 - 1788的部分激动剂特性。