Rataud J, Darche F, Piot O, Stutzmann J M, Böhme G A, Blanchard J C
Biology Department, Rhne-Poulenc Santé, Centre de recherches de Vitry-Alfortville, Vitry sur Seine, France.
Brain Res. 1991 May 10;548(1-2):315-7. doi: 10.1016/0006-8993(91)91139-r.
The effects of systemic treatment with the CCK-B receptor antagonist L-365,260, its 3S-(-) enantiomer and the CCK-A receptor antagonist devazepide were assessed in the plus-maze procedure in mice. L-365,260 (1-1000 micrograms.kg-1 i.p.) produced a dose-dependent increase in the percentage of entries into, and the percentage of time spent in the open arms. Total arm entry was not consistently modified. Neither the 3S-(-) enantiomer of L-365,260 nor devazepide (both administered at 100-10,000 micrograms.kg-1) enhanced the exploratory behavior of mice. These results suggest that CCK-B, rather than CCK-A antagonists may possess 'anxiolytic' properties in mice.
在小鼠的十字迷宫实验中评估了用CCK - B受体拮抗剂L - 365,260、其3S - (-)对映体以及CCK - A受体拮抗剂地伐西匹进行全身治疗的效果。L - 365,260(腹腔注射1 - 1000微克·千克-1)使进入开放臂的百分比和在开放臂中停留的时间百分比呈剂量依赖性增加。总臂进入次数没有持续改变。L - 365,260的3S - (-)对映体和地伐西匹(均以100 - 10000微克·千克-1给药)均未增强小鼠的探索行为。这些结果表明,CCK - B而非CCK - A拮抗剂可能在小鼠中具有“抗焦虑”特性。