Zhang Huiran, Tian Yanfei, Zhang Yan, Wang Yan, Qi Jinlong, Wang Xiangyu, Yuan Yi, Chen Rong, Zhao Yupeng, Liu Chang, Zhou Najing, Liu Lanxin, Hao Han, Du Xiaona, Zhang Hailin
The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Shijiazhuang, China.
Department of Medical and Pharmaceutical Informatics, Hebei Medical University, Shijiazhuang, 050017, Hebei, China.
Transl Stroke Res. 2025 Jan 24. doi: 10.1007/s12975-025-01329-1.
Ischemic stroke is a worldwide disease with high mortality and morbidity. Kv7/KCNQ channels are key modulators of neuronal excitability and microglia function, and activation of Kv7/KCNQ channels has emerged as a potential therapeutic avenue for ischemic stroke. In the present study, we focused on a new Kv7/KCNQ channel opener QO-83 on the stroke outcomes and its therapeutic potential. Transient or distal middle cerebral artery occlusion model was established with C57 mouse to evaluate the role of QO-83. Solitary dose of QO-83 contributes to the microglia inhibition and fibrotic scar mitigation post stroke. QO83 shows prominent effect on reducing infarction area, alleviating cerebral edema, maintaining blood-brain barrier integrity, and enhancing neurogenesis. Single-nucleus RNA sequencing unveils neuroprotection and specific microglial subclusters influenced by QO-83. More importantly, QO83 shows promise in enhancing survival rates with dose dependence. Notably, these protective effects extend beyond the 4-6 h post-reperfusion window. Additionally, continuous dosing of QO-83 correlates with enhanced cognition. In conclusion, this study highlights QO-83 as a protective agent against ischemic brain injury, showcasing its multifaceted effects and potential as a therapeutic strategy.
缺血性中风是一种全球范围内死亡率和发病率都很高的疾病。Kv7/KCNQ通道是神经元兴奋性和小胶质细胞功能的关键调节因子,激活Kv7/KCNQ通道已成为缺血性中风的一种潜在治疗途径。在本研究中,我们聚焦于一种新型Kv7/KCNQ通道开放剂QO-83对中风结局及其治疗潜力的影响。采用C57小鼠建立短暂性或大脑中动脉远端闭塞模型,以评估QO-83的作用。单次给予QO-83有助于中风后抑制小胶质细胞并减轻纤维化瘢痕。QO83在减少梗死面积、减轻脑水肿、维持血脑屏障完整性以及促进神经发生方面显示出显著效果。单核RNA测序揭示了受QO-83影响的神经保护作用和特定的小胶质细胞亚群。更重要的是,QO83在提高生存率方面显示出剂量依赖性的前景。值得注意的是,这些保护作用在再灌注后4 - 6小时的窗口期之外依然存在。此外,持续给予QO-83与认知能力增强相关。总之,本研究强调了QO-83作为一种抗缺血性脑损伤的保护剂,展示了其多方面的作用以及作为一种治疗策略的潜力。