Department of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV, United States; Department of Biochemistry and Microbiology, Oklahoma State University Center for Health Sciences, Tulsa, OK, USA.
Department of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV, United States.
Pharmacol Biochem Behav. 2023 Oct;231:173620. doi: 10.1016/j.pbb.2023.173620. Epub 2023 Aug 23.
Early life adversity in the form of poor postnatal care is a major developmental stressor impacting behavior later in life. Previous studies have shown the impact of early life stress on neurobehavioral abnormalities. Specifically, research has demonstrated how limited bedding and nesting (LBN) materials can cause behavioral deficits in adulthood. There is, however, a limited understanding of how LBN influences sex-specific neurobehavioral adaptation in adolescence, a developmental stage susceptible to psychiatric diseases including substance use disorder. LBN and stress-naive c57BL/6 adolescent male and female mouse offspring were tested for a battery of behaviors including open field, novel object recognition, elevated plus maze, social preference, and morphine-induced conditioned place preference. There was a significant sex-specific deficit in social preference in male mice exposed to LBN compared to stress-naïve counterparts and both LBN males and females had a higher preference towards the drug-paired chamber in the morphine-induced conditioned place preference test. These behavioral deficits were concomitant with sex-specific increases in the transcription factor, Klf9 in the deep cerebellar nuclei (DCN) of males. Further, mRNA levels of the circadian gene Bmal1, which is known to be transcriptionally regulated by Klf9, were decreased in the DCN. Since Bmal1 has recently been implicated in extracellular matrix modulation, we examined perineuronal nets (PNN) and observed depleted PNN in the DCN of males but not female LBN mice. Overall, we provide a novel understanding of how postpartum adversity impinges on the cerebellar extracellular matrix homeostasis, likely, through disruption of the circadian axis by Klf9 that might underlie sex-specific behavioral adaptations in adolescence.
早期生活逆境,如产后护理不良,是影响后期行为的主要发育应激源。先前的研究表明,早期生活应激对神经行为异常有影响。具体而言,研究表明,有限的铺料和巢材如何导致成年期的行为缺陷。然而,对于有限的铺料如何影响青春期特定性别的神经行为适应,人们的理解有限,青春期是易患精神疾病(包括物质使用障碍)的发育阶段。对 LBN 和应激-naive c57BL/6 青春期雄性和雌性小鼠后代进行了一系列行为测试,包括旷场、新物体识别、高架十字迷宫、社交偏好和吗啡诱导的条件位置偏好。与应激-naive 对照组相比,暴露于 LBN 的雄性小鼠的社交偏好存在显著的性别特异性缺陷,而 LBN 雄性和雌性小鼠在吗啡诱导的条件位置偏好测试中对药物配对室的偏好更高。这些行为缺陷伴随着雄性深小脑核 (DCN) 中转录因子 Klf9 的性别特异性增加。此外,已知受 Klf9 转录调控的昼夜节律基因 Bmal1 的 mRNA 水平在 DCN 中降低。由于 Bmal1 最近与细胞外基质调节有关,我们检查了周围神经网 (PNN),并观察到雄性 LBN 小鼠的 DCN 中 PNN 减少,但雌性 LBN 小鼠没有。总的来说,我们提供了一个新的理解,即产后逆境如何通过 Klf9 破坏昼夜节律轴来影响小脑细胞外基质的动态平衡,这可能是青春期特定性别行为适应的基础。