Yaeger Jazmine D W, Achua Justin K, Booth Clarissa D, Khalid Delan, John Megan M, Ledesma Leighton J, Greschke Trent L, Potter Ashley M, Howe Chase B, Krupp Kevin T, Smith Justin P, Ronan Patrick J, Summers Cliff H
Cellular Therapies and Stem Cell Biology Group, Sanford Research, 2301 E. 60th St. N., Sioux Falls, SD, 57104, USA.
Division of Urology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, 80045, USA.
Sci Rep. 2024 Dec 30;14(1):31691. doi: 10.1038/s41598-024-81590-w.
Psychological distress, including anxiety or mood disorders, emanates from the onset of chronic/unpredictable stressful events. Symptoms in the form of maladaptive behaviors are learned and difficult to treat. While the origin of stress-induced disorders seems to be where learning and stress intersect, this relationship and molecular pathways involved remain largely unresolved. The hippocampus, studied for its role in learning, is divided into regions that designate the passage of neuronal signaling during memory formation, including dentate gyrus (DG), CA, CA, and CA. Inputs into these hippocampal subregions, like those from hypothalamic orexinergic neurons, may modify learning outcomes. We have previously shown the orexin system to balance stress states, where receptor subtypes prompt opposing actions on behavior. Here, we explore the connection between hippocampal orexin receptors and learning during stress. In a social stress/learning paradigm separating mice into stress resilient and vulnerable populations, hippocampal OrxR and OrxR transcription is regulated in a phenotype-dependent fashion. We further identified OrxR as highly expressed in the hilus of DG, while OrxR is abundant in CA. Finally, we designed an experiment where mice were provided prior exposure to a stressful environment, which ultimately modified behavior, as well as transcription of hippocampal orexin receptors.
心理困扰,包括焦虑或情绪障碍,源于慢性/不可预测的应激事件的发作。适应不良行为形式的症状是习得的且难以治疗。虽然应激诱导障碍的起源似乎是学习与应激的交叉点,但这种关系以及所涉及的分子途径在很大程度上仍未得到解决。海马体因其在学习中的作用而受到研究,它被分为在记忆形成过程中指定神经元信号传递通道的区域,包括齿状回(DG)、CA1、CA2和CA3。进入这些海马体亚区域的输入,如下丘脑食欲素能神经元的输入,可能会改变学习结果。我们之前已经表明食欲素系统可平衡应激状态,其中受体亚型对行为产生相反的作用。在这里,我们探讨海马体食欲素受体与应激期间学习之间的联系。在将小鼠分为应激抗性和易感性群体的社会应激/学习范式中,海马体的食欲素受体1(OrxR1)和食欲素受体2(OrxR2)转录以表型依赖的方式受到调节。我们进一步确定食欲素受体1在齿状回的门区高度表达,而食欲素受体2在CA1区丰富。最后,我们设计了一个实验,让小鼠预先暴露于应激环境中,这最终改变了行为以及海马体食欲素受体的转录。