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Published on: July 29, 2019
Loss of glymphatic homeostasis in heart failure
Marios Kritsilis1,2, Lotte Vanherle1,2,3, Marko Rosenholm4,5,6
1Department of Experimental Medical Science, Lund University, 22362 Lund, Sweden.
Insights
Heart failure impairs brain waste removal by altering glymphatic function, driven by increased arterial pulsatility but not proportional clearance. This suggests cerebral blood flow is key to preventing cognitive decline.
Area of Science:
- Neuroscience
- Cardiovascular Science
- Physiology
Background:
- Heart failure reduces cerebral blood flow, leading to cognitive decline and neurodegeneration.
- The glymphatic system clears brain waste; its dysfunction is linked to neurodegeneration.
Purpose of the Study:
- To investigate the impact of heart failure with reduced ejection fraction on glymphatic system function in a mouse model.
- To explore the relationship between cerebral blood flow, arterial pulsatility, and glymphatic function in heart failure.
Main Methods:
- Myocardial infarction induced heart failure in mice.
- Dynamic contrast-enhanced MRI and two-photon microscopy assessed glymphatic influx and arterial pulsatility.
- Brain parenchyma volume and protein clearance were quantified.
Main Results:
- Heart failure increased glymphatic influx and cerebral arterial pulsatility 12 weeks post-myocardial infarction.
- Protein clearance did not increase proportionally with influx, indicating dysregulated brain fluid dynamics.
- A correlation was observed between brain clearance and cerebral blood flow.
Conclusions:
- Cerebral blood flow is a critical regulator of glymphatic system function.
- Heart failure-induced alterations in glymphatic dynamics may contribute to cognitive decline.
- Further research is needed to understand cardiovascular disease effects on brain clearance mechanisms.
Abstract:
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.
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