State Key Laboratory of Chemical Oncogenomics, Shenzhen Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Shenzhen, 518055, China.
School of Medicine, Dali University, Dali, 671000, China.
Biochem Biophys Res Commun. 2024 Nov 19;734:150789. doi: 10.1016/j.bbrc.2024.150789. Epub 2024 Oct 2.
Children with epilepsy are particularly vulnerable to anxiety disorders, where these disorders are frequently underdiagnosed and untreated. Despite the high prevalence of anxiety in epilepsy, the underlying neurobiological mechanisms are not fully understood. The medial prefrontal cortex (mPFC) and ventral hippocampus (vHPC) are key brain regions implicated in the genesis and modulation of anxiety, and their interactions play a crucial role in emotional processing including anxiety. We utilized a pilocarpine-induced epilepsy model in young mice (7 weeks old) to assess anxiety-like behaviors using the open field test (OFT), light/dark box, and elevated plus maze (EPM). Local field potential (LFP) recordings were conducted to examine theta power and coherence between the mPFC and vHPC. LFP recordings revealed significantly altered theta power variation in both the mPFC and vHPC during exposure to anxiogenic contexts, suggesting the involvement of these regions in anxiety in the young epileptic mice. Notably, theta-frequency synchrony between the mPFC and vHPC was not significantly altered in the young epileptic mice, indicating that altered theta power rather than inter-regional synchrony may underlie anxiety behaviors in young epileptic mice. Furthermore, we demonstrated that chemogenetic inhibition of excitatory neurons in the mPFC and vHPC reduced anxiety levels in young epileptic mice. Altogether, our findings highlight the critical contributions of mPFC and vHPC to the pathogenesis of comorbid anxiety in epilepsy. These findings underscore the potential therapeutic significance of modulating the activity in these two regions as means to alleviate anxiety in a youth epilepsy population.
患有癫痫的儿童尤其容易患焦虑症,但这些疾病常常被漏诊和未得到治疗。尽管癫痫患者中焦虑症的患病率很高,但潜在的神经生物学机制仍不完全清楚。内侧前额叶皮层(mPFC)和腹侧海马体(vHPC)是与焦虑症的发生和调节有关的关键脑区,它们的相互作用在情绪处理中起着至关重要的作用,包括焦虑症。我们利用匹鲁卡品诱导的年轻小鼠(7 周龄)癫痫模型,通过旷场试验(OFT)、明暗箱和高架十字迷宫(EPM)评估焦虑样行为。进行局部场电位(LFP)记录以检查 mPFC 和 vHPC 之间的θ功率和相干性。LFP 记录显示,在焦虑环境下,mPFC 和 vHPC 的θ功率变化明显改变,表明这些区域参与了年轻癫痫小鼠的焦虑症。值得注意的是,年轻癫痫小鼠 mPFC 和 vHPC 之间的θ频率同步性没有明显改变,表明改变的θ功率而不是区域间同步性可能是年轻癫痫小鼠焦虑行为的基础。此外,我们证明了 mPFC 和 vHPC 中的兴奋性神经元的化学遗传抑制可降低年轻癫痫小鼠的焦虑水平。总之,我们的发现强调了 mPFC 和 vHPC 对癫痫共患焦虑症发病机制的关键贡献。这些发现强调了调节这两个区域活动作为减轻青少年癫痫人群焦虑症的潜在治疗意义。