Altered linear coupling between stimulus-evoked blood flow and oxygen metabolism in the aging human brain

Author:

Turner Monroe P12,Zhao Yuguang12,Abdelkarim Dema12,Liu Peiying3,Spence Jeffrey S12,Hutchison Joanna L12,Sivakolundu Dinesh K14,Thomas Binu P5,Hubbard Nicholas A6,Xu Cuimei3,Taneja Kamil3,Lu Hanzhang3,Rypma Bart12

Affiliation:

1. School of Behavioral and Brain Sciences , University of Texas at Dallas, Richardson, TX 75080, USA

2. Center for BrainHealth , University of Texas at Dallas, Dallas, TX, 75235, USA

3. Department of Radiology and Radiological Science , Johns Hopkins University, Baltimore, MD 21287, USA

4. Department of Biological Sciences , University of Texas at Dallas, Richardson, TX, 75080, USA

5. Advanced Imaging Research Center , University of Texas Southwestern Medical Center, Dallas, TX 75235, USA

6. Department of Psychology , Center for Brain, Biology, and Behavior, University of Nebraska, Lincoln, NE 68588, USA

Abstract

Abstract Neural-vascular coupling (NVC) is the process by which oxygen and nutrients are delivered to metabolically active neurons by blood vessels. Murine models of NVC disruption have revealed its critical role in healthy neural function. We hypothesized that, in humans, aging exerts detrimental effects upon the integrity of the neural-glial-vascular system that underlies NVC. To test this hypothesis, calibrated functional magnetic resonance imaging (cfMRI) was used to characterize age-related changes in cerebral blood flow (CBF) and oxygen metabolism during visual cortex stimulation. Thirty-three younger and 27 older participants underwent cfMRI scanning during both an attention-controlled visual stimulation task and a hypercapnia paradigm used to calibrate the blood-oxygen-level-dependent signal. Measurement of stimulus-evoked blood flow and oxygen metabolism permitted calculation of the NVC ratio to assess the integrity of neural-vascular communication. Consistent with our hypothesis, we observed monotonic NVC ratio increases with increasing visual stimulation frequency in younger adults but not in older adults. Age-related changes in stimulus-evoked cerebrovascular and neurometabolic signal could not fully explain this disruption; increases in stimulus-evoked neurometabolic activity elicited corresponding increases in stimulus-evoked CBF in younger but not in older adults. These results implicate age-related, demand-dependent failures of the neural-glial-vascular structures that comprise the NVC system.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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