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Neurobehav Toxicol Teratol. 1986 Sep-Oct;8(5):447-52.
Male offspring of hooded Lister rats were fostered at birth to form experimental litters of eight. Within each litter pups were randomly allocated among drug groups. Administration of clonazepam (1-5 mg/kg/day) to pups from neonatal days 1-21 resulted in high mortality, at least partly due to impaired ultrasonic calling. Pups treated with 0.1, 0.5 or 1 mg/kg/day throughout the preweaning period were then tested undrugged during adolescence to assess any lasting behavioral changes. There were no significant changes in the social interaction test or in the acquisition or retention of a passive avoidance task. However, neonatal treatment with clonazepam (0.1 mg/kg) did produce significantly less exploratory head-dipping and locomotor activity in a holeboard. This dose also enhanced offensive behaviors when rats were resident in their home-cages and confronted with an intruder, but increased submissive behaviors when the treated rats were intruding into another rat's territory. Treatment with higher doses of clonazepam (0.5 and 1 mg/kg) produced more dominance behaviors when the pups were intruders. Since the main behavioral changes were found in the lowest dose group, which did not show any weight loss, they are unlikely to be secondary to changes in the risk of mortality.
带帽利斯特大鼠的雄性后代在出生时被寄养,以形成每组八只的实验性一窝幼崽。在每一窝幼崽中,幼崽被随机分配到不同药物组。从出生后第1天到第21天给幼崽施用氯硝西泮(1 - 5毫克/千克/天)导致高死亡率,至少部分原因是超声波发声受损。然后,在断奶前整个时期用0.1、0.5或1毫克/千克/天治疗的幼崽在青春期不服用药物进行测试,以评估任何持续的行为变化。在社交互动测试或被动回避任务的习得或保持方面没有显著变化。然而,出生时用氯硝西泮(0.1毫克/千克)治疗确实在穿洞板实验中产生显著更少的探索性探头和运动活动。当大鼠在其笼舍中并面对入侵者时,该剂量也增强了攻击行为,但当经治疗的大鼠侵入另一只大鼠的领地时增加了顺从行为。当幼崽作为入侵者时,用更高剂量的氯硝西泮(0.5和1毫克/千克)治疗产生更多的支配行为。由于主要行为变化在最低剂量组中被发现,且该组未显示任何体重减轻,这些变化不太可能是死亡率风险变化的继发结果。