Details

Autor(en) / Beteiligte

• Turner, Monroe P
• Zhao, Yuguang
• Abdelkarim, Dema
• Liu, Peiying
• Spence, Jeffrey S
• Hutchison, Joanna L
• Sivakolundu, Dinesh K
• Thomas, Binu P
• Hubbard, Nicholas A
• Xu, Cuimei
• Taneja, Kamil
• Lu, Hanzhang
• Rypma, Bart

Titel

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

Ist Teil von

• Cerebral cortex (New York, N.Y. 1991), 2022-12, Vol.33 (1), p.135-151

Ort / Verlag

United States: Oxford University Press

Erscheinungsjahr

2022

Quelle

Oxford Journals 2020 Medicine

Beschreibungen/Notizen

• 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.