Wu Yingqing, Deng Qin, Wei Ranran, Chen Sen, Ding Fusheng, Yu Haipeng, Hu Ning, Hao Shilei, Wang Bochu
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, No. 174, Shapingba Main Street, Chongqing, 400030, China.
Analytical and Testing Center, Chongqing University, Chongqing, 400030, China.
Transl Stroke Res. 2025 Jun;16(3):757-774. doi: 10.1007/s12975-024-01257-6. Epub 2024 May 15.
Intracerebral hemorrhage (ICH) imposes a significant burden on patients, and the volume of hematoma plays a crucial role in determining the severity and prognosis of ICH. Although significant recent progress has been made in understanding the cellular and molecular mechanisms of surrounding brain tissue in ICH, our current knowledge regarding the precise impact of hematoma volumes on neural circuit damage remains limited. Here, using a viral tracing technique in a mouse model of striatum ICH, two distinct patterns of injury response were observed in upstream connectivity, characterized by both linear and nonlinear trends in specific brain areas. Notably, even low-volume hematomas had a substantial impact on downstream connectivity. Neurons in the striatum-ICH region exhibited heightened excitability, evidenced by electrophysiological measurements and changes in metabolic markers. Furthermore, a strong linear relationship (R = 0.91) was observed between hematoma volumes and NFL damage, suggesting a novel biochemical index for evaluating changes in neural injury. RNA sequencing analysis revealed the activation of the MAPK signaling pathway following hematoma, and the addition of MAPK inhibitor revealed a decrease in neuronal circuit damage, leading to alleviation of motor dysfunction in mice. Taken together, our study highlights the crucial role of hematoma size as a determinant of circuit injury in ICH. These findings have important implications for clinical evaluations and treatment strategies, offering opportunities for precise therapeutic approaches to mitigate the detrimental effects of ICH and improve patient outcomes.
脑出血(ICH)给患者带来了沉重负担,血肿体积在决定ICH的严重程度和预后方面起着关键作用。尽管最近在理解ICH周围脑组织的细胞和分子机制方面取得了重大进展,但我们目前关于血肿体积对神经回路损伤的确切影响的认识仍然有限。在此,我们在纹状体ICH小鼠模型中使用病毒示踪技术,在上游连接性方面观察到两种不同的损伤反应模式,其特征是特定脑区存在线性和非线性趋势。值得注意的是,即使是小体积血肿也对下游连接性有重大影响。纹状体-ICH区域的神经元表现出兴奋性增强,这通过电生理测量和代谢标志物的变化得到证实。此外,在血肿体积与神经丝轻链(NFL)损伤之间观察到强线性关系(R = 0.91),这表明存在一种用于评估神经损伤变化的新型生化指标。RNA测序分析显示血肿后丝裂原活化蛋白激酶(MAPK)信号通路被激活,添加MAPK抑制剂可减少神经元回路损伤,从而减轻小鼠的运动功能障碍。综上所述,我们的研究强调了血肿大小作为ICH中回路损伤决定因素的关键作用。这些发现对临床评估和治疗策略具有重要意义,并为减轻ICH有害影响和改善患者预后的精确治疗方法提供了机会。