Zoology Department, University of Oxford, South Parks Road, Oxford OX1 3PS, UK.
Behav Brain Res. 2010 Jul 29;211(1):96-104. doi: 10.1016/j.bbr.2010.03.018. Epub 2010 Mar 15.
Stereotypic behaviours are common in animals in impoverished housing, arising from two complementary processes: (1) thwarted attempts to perform motivated behaviours; (2) forebrain dysfunction impeding normal behavioural inhibition. When enriched animals are moved to impoverished housing, they are sometimes protected against developing stereotypic behaviour, but in other cases become even more stereotypic than animals housed lifelong without enrichment. Negative contrast-induced frustration must occur in both scenarios. We hypothesise that sustained behavioural responses to this frustration are prevented in the former by normalised forebrain function, but exacerbated in the latter by forebrain dysfunction. ICRCD-1 mice reared in enriched or standard cages were re-caged at 3 months to standard conditions. Here, previously-enriched mice became far more stereotypic than mice reared from birth in such conditions. To investigate the role of frustration, we assessed both corticosterone output and motivation (break-point) to regain enrichments. We also assessed perseveration via extinction learning. As predicted, previously-enriched mice were as perseverative as standard-raised mice, and frustration seemed to play a causal role in their exacerbated stereotypic behaviour. Previously-enriched mice showed higher motivations to access enrichments, and only in this group did these correlate with corticosterone levels after re-caging; furthermore only in previously-enriched mice did corticosterone responses to re-caging predict stereotypic behaviour 30 days later (males only). All results need replicating and further investigation. However, they suggest for the first time that individual risk factors related to the HPA axis predict stereotypic behaviour following enrichment-removal, and that previously-enriched mice have lasting motivational differences from standard-raised mice, suggesting sustained behavioural effects related to the frustration of enrichment-loss.
刻板行为在贫困环境中的动物中很常见,它源于两个互补的过程:(1)动机行为受挫;(2)大脑前皮质功能障碍阻碍正常的行为抑制。当被丰富环境饲养的动物被转移到贫困环境中时,它们有时可以免受刻板行为的影响,但在其他情况下,它们会变得比那些终生没有被丰富环境饲养的动物更加刻板。在这两种情况下,都必须发生负性对比引起的挫折。我们假设,在前一种情况下,正常的大脑前皮质功能阻止了对这种挫折的持续行为反应,而在后一种情况下,大脑前皮质功能障碍则加剧了这种反应。在丰富或标准笼中饲养的 ICRCD-1 小鼠在 3 个月时被重新放回标准条件的笼子中。在这里,以前在丰富环境中饲养的小鼠比那些从出生就在这种条件下饲养的小鼠更加刻板。为了研究挫折的作用,我们评估了皮质酮的输出和动机(断点)来重新获得丰富环境。我们还通过消退学习评估了坚持性。正如预测的那样,以前在丰富环境中饲养的小鼠和在标准环境中饲养的小鼠一样坚持,挫折似乎在它们加剧的刻板行为中起因果作用。以前在丰富环境中饲养的小鼠对获得丰富环境的动机更高,而且只有在这个组中,这些动机与重新饲养后的皮质酮水平相关;此外,只有在以前在丰富环境中饲养的小鼠中,重新饲养后的皮质酮反应预测了 30 天后的刻板行为(仅雄性)。所有结果都需要复制和进一步研究。然而,它们首次表明,与 HPA 轴相关的个体风险因素可以预测丰富环境去除后的刻板行为,并且以前在丰富环境中饲养的小鼠与标准环境中饲养的小鼠有持久的动机差异,这表明与丰富环境丧失相关的挫折会产生持续的行为影响。