| Literature DB >> 31810839 |
Susanne J van Veluw1, Steven S Hou2, Maria Calvo-Rodriguez2, Michal Arbel-Ornath2, Austin C Snyder2, Matthew P Frosch3, Steven M Greenberg4, Brian J Bacskai2.
Abstract
Paravascular drainage of solutes, including β-amyloid (Aβ), appears to be an important process in brain health and diseases such as Alzheimer's disease (AD) and cerebral amyloid angiopathy (CAA). However, the major driving force for clearance remains largely unknown. Here we used in vivo two-photon microscopy in awake head-fixed mice to assess the role of spontaneous vasomotion in paravascular clearance. Vasomotion correlated with paravascular clearance of fluorescent dextran from the interstitial fluid. Increasing the amplitude of vasomotion by means of visually evoked vascular responses resulted in increased clearance rates in the visual cortex of awake mice. Evoked vascular reactivity was impaired in mice with CAA, which corresponded to slower clearance rates. Our findings suggest that low-frequency arteriolar oscillations drive drainage of solutes. Targeting naturally occurring vasomotion in patients with CAA or AD may be a promising early therapeutic option for prevention of Aβ accumulation in the brain.Entities:
Keywords: Alzheimer’s disease; cerebral amyloid angiopathy; functional hyperemia; glymphatics; intra-mural peri-arterial drainage; perivascular space; vascular smooth muscle cells; vasomotion
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Year: 2019 PMID: 31810839 PMCID: PMC7028316 DOI: 10.1016/j.neuron.2019.10.033
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173