Ai Li, Usman Muhammad, Lu Hong
Department of Postdoctoral Research Workstation, Central Hospital Affiliated to Chongqing University of Technology, Chongqing University of Technology, Gonglian yicun No.1 street lijiatuo, Banan district, Chongqing, 400054, P.R. China.
Department of Postdoctoral Research Workstation, Kunming Children's Hospital, 28 Shulin St, Kunming, Yunnan, China.
Sci Rep. 2025 May 16;15(1):17040. doi: 10.1038/s41598-025-02071-2.
Traumatic brain injury (TBI) has a high disability rate and a high fatality rate. Traumatic penumbra (TP) is a potentially reversible area around the core area of brain trauma with cerebral edema as the main pathological change, which is a breakthrough to improve the prognosis of patients with TBI and reduce the mortality and disability rate of TBI. Unfortunately, the pathophysiological mechanism of TP is still not fully understood. In this study, we established a moderate traumatic brain injury model in rats and detected pathological molecular markers in TP. Protein content of IgG, VEGF, and AQP4 were detect respectively by HE, Immunofluorescence, and western blot. To investigate the time-varying characteristics of TP, to provide a reference for research and development and screening of TBI targeted drugs. Our experiment showed mainly intracellular edema and vascular edema in TP, first intracellular then vascular edema was dominant. IgG, VEGF, and AQP4 in TP increased significantly. On the second day, AQP4 decreased, and third day AQP4 increased again. We found that in the early stage of TBI cerebral edema developed and it is related to the increase of BBB permeability, upregulation of VEGF and AQP4. Suggesting potential targets for treatment of TP.
创伤性脑损伤(TBI)致残率和致死率高。创伤性半暗带(TP)是脑外伤核心区域周围具有潜在可逆性的区域,主要病理改变为脑水肿,这是改善TBI患者预后、降低TBI死亡率和致残率的一个突破点。遗憾的是,TP的病理生理机制仍未完全明确。在本研究中,我们建立了大鼠中度创伤性脑损伤模型,并检测了TP中的病理分子标志物。分别通过苏木精-伊红染色(HE)、免疫荧光和蛋白质免疫印迹法检测免疫球蛋白G(IgG)、血管内皮生长因子(VEGF)和水通道蛋白4(AQP4)的蛋白含量。旨在研究TP的时变特征,为TBI靶向药物的研发和筛选提供参考。我们的实验显示,TP主要表现为细胞内水肿和血管性水肿,初期以细胞内水肿为主,随后血管性水肿占主导。TP中的IgG、VEGF和AQP4显著增加。在第二天,AQP4下降,第三天AQP4再次升高。我们发现,在TBI早期脑水肿开始形成,这与血脑屏障(BBB)通透性增加、VEGF和AQP4上调有关。提示了TP的潜在治疗靶点。