Kritsilis Marios, Vanherle Lotte, Rosenholm Marko, In 't Zandt René, Yao Yuan, Swanberg Kelley M, Weikop Pia, Gottschalk Michael, Shanbhag Nagesh C, Luo Jiebo, Boster Kimberly, Nedergaard Maiken, Meissner Anja, Lundgaard Iben
Department of Experimental Medical Science, Lund University, 22362 Lund, Sweden.
Wallenberg Center for Molecular Medicine, Lund University, 22184 Lund, Sweden.
Brain. 2025 Mar 6;148(3):985-1000. doi: 10.1093/brain/awae411.
Heart failure is associated with progressive reduction in cerebral blood flow and neurodegenerative changes leading to cognitive decline. The glymphatic system is crucial for the brain's waste removal, and its dysfunction is linked to neurodegeneration. In this study, we used a mouse model of heart failure, induced by myocardial infarction, to investigate the effects of heart failure with reduced ejection fraction on the brain's glymphatic function. Using dynamic contrast-enhanced MRI and high-resolution fluorescence microscopy, we found increased solute influx from the CSF spaces to the brain, i.e. glymphatic influx, at 12 weeks post-myocardial infarction. Two-photon microscopy revealed that cerebral arterial pulsatility, a major driver of the glymphatic system, was potentiated at this time point, and could explain this increase in glymphatic influx. However, clearance of proteins from the brain parenchyma did not increase proportionately with influx, while a relative increase in brain parenchyma volume was found at 12 weeks post-myocardial infarction, suggesting dysregulation of brain fluid dynamics. Additionally, our results showed a correlation between brain clearance and cerebral blood flow. These findings highlight the role of cerebral blood flow as a key regulator of the glymphatic system, suggesting its involvement in the development of brain disorders associated with reduced cerebral blood flow. This study paves the way for future investigations into the effects of cardiovascular diseases on the brain's clearance mechanisms, which may provide novel insights into the prevention and treatment of cognitive decline.
心力衰竭与脑血流量的逐渐减少以及导致认知衰退的神经退行性变化相关。类淋巴系统对于大脑废物清除至关重要,其功能障碍与神经退行性变有关。在本研究中,我们使用了由心肌梗死诱导的心力衰竭小鼠模型,以研究射血分数降低的心力衰竭对大脑类淋巴功能的影响。通过动态对比增强磁共振成像和高分辨率荧光显微镜,我们发现在心肌梗死后12周,从脑脊液间隙到大脑的溶质流入增加,即类淋巴流入增加。双光子显微镜显示,类淋巴系统的主要驱动因素脑动脉搏动性在这个时间点增强,并且可以解释类淋巴流入的这种增加。然而,脑实质中蛋白质的清除并没有与流入成比例增加,而在心肌梗死后12周发现脑实质体积相对增加,提示脑流体动力学失调。此外,我们的结果显示脑清除与脑血流量之间存在相关性。这些发现突出了脑血流量作为类淋巴系统关键调节因子的作用,表明其参与了与脑血流量减少相关的脑部疾病的发展。本研究为未来研究心血管疾病对大脑清除机制的影响铺平了道路,这可能为认知衰退的预防和治疗提供新的见解。