Department of Human Anatomy and Histoembryology, Binzhou Medical University, Yantai, China.
Department of Pathology, Shandong First Medical University, Jinan, China.
Biochem Biophys Res Commun. 2022 Apr 30;602:142-148. doi: 10.1016/j.bbrc.2022.02.108. Epub 2022 Mar 3.
Dysregulation of the dorsal raphe nucleus (DRN) has been revealed to contribute to cognitive and arousal impairments associated with post-traumatic stress disorder (PTSD) in an animal model. In our research an acute exposure to single prolonged stress (SPS) was used to establish PTSD rat model and the effects related to cell-cycle signaling pathway in DRN were examined. Apoptosis in DRN was detected by TUNEL staining, showing that DRN apoptosis number was sharply increased after SPS. SPS triggered cell-cycle CDK4/CyclinD1-pRB-E2F1 signal pathway. Treatment with CDK4 inhibitor Abemaciclib successfully attenuated the DRN apoptosis and rescued decreased spatial learning and memory abilities in SPS rats, indicating that activation of CDK4/CyclinD1-pRB-E2F1 pathway was involved in DRN apoptosis, which may be one of the pathogenesis for PTSD.
背缝核(DRN)的失调已被证明与创伤后应激障碍(PTSD)相关的认知和觉醒损伤有关,在动物模型中也是如此。在我们的研究中,急性单次延长应激(SPS)用于建立 PTSD 大鼠模型,并研究了与 DRN 细胞周期信号通路相关的作用。通过 TUNEL 染色检测 DRN 中的细胞凋亡,结果表明 SPS 后 DRN 细胞凋亡数量急剧增加。SPS 触发细胞周期 CDK4/CyclinD1-pRB-E2F1 信号通路。用 CDK4 抑制剂 Abemaciclib 治疗可成功减轻 DRN 细胞凋亡,并挽救 SPS 大鼠空间学习和记忆能力下降,表明 CDK4/CyclinD1-pRB-E2F1 通路的激活参与了 DRN 细胞凋亡,这可能是 PTSD 的发病机制之一。