Pontifical Catholic University of Rio Grande do Sul (PUCRS), Brain Institute (InsCer), Developmental Cognitive Neuroscience Lab, Porto Alegre, RS, Brazil.
Louisiana State University, Health Sciences Center, Department of Physiology, New Orleans, United States.
Psychoneuroendocrinology. 2019 Jan;99:8-19. doi: 10.1016/j.psyneuen.2018.08.032. Epub 2018 Aug 26.
While increasing evidence posits poor decision-making as a central feature of mental disorders, very few studies investigated the effects of early-life stress (ELS) on specific components of reward-related choice behaviors. Risk-taking (RT) involves the exposure to some danger, or negative consequences, in order to achieve a goal-directed behavior. Such behaviors are likely to be preceded by risk-assessment (RA), which is a dynamic cognitive process involving the acquisition of information in potentially dangerous situations. Here, we investigated the effects of being raised in impoverished housing conditions during early life (P2-P9) on RT, RA and dopaminergic and corticotrophinergic gene expression of adolescent male and female mice. Phenotypes were assessed by two protocols: the elevated plus-maze (EPM) and the predator-odor risk-taking (PORT). We found decreased RA in mice exposed to impoverished housing in the absence of a reward (EPM), with a more pronounced effect among females. Moreover, when exposed to a predatory olfactory cue, increased RT was observed in these females in a reward-related task (PORT), as well as decreased HPA axis responsivity. This sex-specific behavioral effect was associated with increased Crfr1 mRNA expression in the medial prefrontal cortex (mPFC) and higher levels of the histone mark H3R2, a histone modification known to be involved in transcriptional activation, within the promoter of the Crfr1 gene. These findings revealed that ELS exposure can impair the acquisition of environmental information in dangerous situations and increase RT in reward-related scenarios among females, with an important role regarding epigenetic regulation of the Crfr1 gene.
虽然越来越多的证据表明决策能力差是精神障碍的一个核心特征,但很少有研究调查早期生活应激 (ELS) 对与奖励相关的选择行为的特定成分的影响。冒险行为 (RT) 涉及到为了实现目标导向的行为而暴露于某些危险或负面后果中。这种行为很可能是在风险评估 (RA) 之前发生的,RA 是一个动态的认知过程,涉及在潜在危险的情况下获取信息。在这里,我们研究了在生命早期(P2-P9)生活在贫困住房条件下对雄性和雌性青少年小鼠的 RT、RA 和多巴胺能和促肾上腺皮质激素基因表达的影响。通过两种方案评估表型:高架十字迷宫(EPM)和捕食者气味冒险行为(PORT)。我们发现,在没有奖励的情况下,暴露于贫困住房中的小鼠的 RA 减少,而雌性小鼠的影响更为明显。此外,当暴露于捕食者嗅觉线索时,这些雌性小鼠在与奖励相关的任务(PORT)中表现出 RT 增加,同时 HPA 轴反应性降低。这种性别特异性的行为效应与中前额叶皮层(mPFC)中 Crfr1 mRNA 表达增加以及 Crfr1 基因启动子中 H3R2 等组蛋白标记物水平升高有关,H3R2 是一种已知参与转录激活的组蛋白修饰。这些发现表明,ELS 暴露会损害在危险情况下获取环境信息的能力,并增加雌性动物在与奖励相关的情境中的 RT,这对 Crfr1 基因的表观遗传调控具有重要作用。