Furukawa S, Takagi H, Iwasaki T
Institute of Psychology, University of Tsukuba, Ibaraki, Japan.
Yakubutsu Seishin Kodo. 1987 Jun;7(2):307-12.
The present study was designed to investigate the effects of chlordiazepoxide (CDP; 5 and 10 mg/kg, ip) on one-trial step-through passive avoidance learning in Wistar-Imamichi (W-I) and F344/Du (F) strain rats. Step-through latency and the time spent in safety-box were significantly longer in W-I than F rats. The number of animals that attained the 300-s criterion was also larger in W-I than F rats. Therefore, it was concluded that W-I rats showed superior performance in the passive avoidance task as compared to F rats. Taken together, these and the previous results (Iwasaki et al, 1984) that F rats acquired the active avoidance learning more easily than W-I rats, the differences of performance in the two strains would reflect differences of strain-specific response patterns in aversive situations, but not of learning ability. Further, CDP produced a dose-dependent state-dependency in W-I but not in F rats. These strain differences in the effect of CDP were considered to derive from differences in sensitivity to the drug, rather than in the baseline performance level, because comparable strain differences in drug effect were reported in active avoidance learning.
本研究旨在探讨氯氮卓(CDP;5和10毫克/千克,腹腔注射)对Wistar-Imamichi(W-I)和F344/Du(F)品系大鼠一次性被动回避学习的影响。W-I大鼠的穿箱潜伏期和在安全箱内停留的时间显著长于F大鼠。达到300秒标准的动物数量在W-I大鼠中也多于F大鼠。因此,得出结论,与F大鼠相比,W-I大鼠在被动回避任务中表现更优。综合这些结果以及之前的结果(岩崎等人,1984年),即F大鼠比W-I大鼠更容易习得主动回避学习,这两个品系在行为表现上的差异将反映出在厌恶情境中品系特异性反应模式的差异,而非学习能力的差异。此外,CDP在W-I大鼠中产生了剂量依赖性的状态依赖性,而在F大鼠中则没有。CDP效应的这些品系差异被认为源于对药物敏感性的差异,而非基线表现水平的差异,因为在主动回避学习中也报道了类似的药物效应品系差异。