Stimulus-evoked changes in cerebral vessel diameter: A study in healthy humans

The high metabolic demand of neuronal tissue, coupled with its relatively low energy storage capacity, requires that increases in neuronal activation are quickly matched with increased blood flow to ensure efficient supply of oxygen and nutrients to the tissue. For this to occur, dilation of nearby...

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Published inJournal of cerebral blood flow and metabolism Vol. 38; no. 3; pp. 528 - 539
Main Authors Bizeau, Alexandre, Gilbert, Guillaume, Bernier, Michaël, Huynh, Minh Tung, Bocti, Christian, Descoteaux, Maxime, Whittingstall, Kevin
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 01.03.2018
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Summary:The high metabolic demand of neuronal tissue, coupled with its relatively low energy storage capacity, requires that increases in neuronal activation are quickly matched with increased blood flow to ensure efficient supply of oxygen and nutrients to the tissue. For this to occur, dilation of nearby arterioles must be coordinated with the dilation of larger upstream feeding arteries. As it stands, the exact spatial extent of such dilation in humans is unknown. Using non-invasive time-of-flight magnetic resonance angiography in healthy participants, we developed an automatic methodology for reconstructing cerebral arterial vessels and quantifying their diameter on a voxel-by-voxel basis. Specifically, we isolated the posterior cerebral artery (PCA) supplying each occipital lobe and quantified its vasodilation induced by visual stimulation. Stimulus-induced changes were strongest (∼30%) near primary visual cortex and progressively decreased in a non-linear fashion as a function of distance. Surprisingly, weak – albeit significant – changes (∼2%) were observed ∼70 mm from the visual cortex. This demonstrates that visual stimulation modulates vascular tone along the bulk of the PCA segment, and thus may have important implications for our understanding of functional hyperemia in healthy and diseased states.
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ISSN:0271-678X
1559-7016
DOI:10.1177/0271678X17701948