Journal of Neuroscience· 2013Q1
Cerebral Arterial Pulsation Drives Paravascular CSF–Interstitial Fluid Exchange in the Murine Brain
- 1,350citations
- Q1SCImago
- 2013year
Short summary
Cerebral arterial pulsation directly drives the flow of cerebrospinal fluid (CSF) into the brain along paravascular spaces, facilitating the clearance of waste products like amyloid-beta.
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Key points
- Cerebral arterial pulsation was directly visualized and quantified in mice using two-photon microscopy.
- Internal carotid artery ligation reduced arterial pulsatility by ~50%, slowing paravascular CSF-ISF exchange.
- Dobutamine increased penetrating artery pulsatility by ~60%, accelerating paravascular CSF-ISF exchange.
- Arterial pulsation is identified as a primary driver of CSF influx and interstitial fluid clearance.
AI-generated from the title and abstract; the full text is not read.
Abstract
CSF from the subarachnoid space moves rapidly into the brain along paravascular routes surrounding penetrating cerebral arteries, exchanging with brain interstitial fluid (ISF) and facilitating the clearance of interstitial solutes, such as amyloid β, in a pathway that we have termed the "glymphatic" system. Prior reports have suggested that paravascular bulk flow of CSF or ISF may be driven by arterial pulsation. However, cerebral arterial pulsation could not be directly assessed. In the present study, we use in vivo two-photon microscopy in mice to visualize vascular wall pulsatility in penetrating intracortical arteries. We observed that unilateral ligation of the internal carotid artery significantly reduced arterial pulsatility by ~50%, while systemic administration of the adrenergic agonist dobutamine increased pulsatility of penetrating arteries by ~60%. When paravascular CSF-ISF exchange was evaluated in real time using in vivo two-photon and ex vivo fluorescence imaging, we observed that internal carotid artery ligation slowed the rate of paravascular CSF-ISF exchange, while dobutamine increased the rate of paravascular CSF-ISF exchange. These findings demonstrate that cerebral arterial pulsatility is a key driver of paravascular CSF influx into and through the brain parenchyma, and suggest that changes in arterial pulsatility may contribute to accumulation and deposition of toxic solutes, including amyloid β, in the aging brain.
The authors' abstract, as published at the source. Journal of Neuroscience, 2013 · DOI ↗
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Field: Cellular and Molecular Neuroscience
Cellular and Molecular NeuroscienceNeuroscience