Neurovascular coupling mechanisms in health and neurovascular uncoupling in Alzheimer’s disease

Author:

Zhu Winston M1ORCID,Neuhaus Ain2,Beard Daniel J23,Sutherland Brad A4,DeLuca Gabriele C5

Affiliation:

1. Oxford Medical School, University of Oxford , Oxford , UK

2. Acute Stroke Programme, Radcliffe Department of Medicine, University of Oxford , Oxford , UK

3. School of Biomedical Sciences and Pharmacy, University of Newcastle , Newcastle , Australia

4. Tasmanian School of Medicine, College of Health and Medicine, University of Tasmania , Hobart , Australia

5. Nuffield Department of Clinical Neurosciences, University of Oxford , Oxford , UK

Abstract

Abstract To match the metabolic demands of the brain, mechanisms have evolved to couple neuronal activity to vasodilation, thus increasing local cerebral blood flow and delivery of oxygen and glucose to active neurons. Rather than relying on metabolic feedback signals such as the consumption of oxygen or glucose, the main signalling pathways rely on the release of vasoactive molecules by neurons and astrocytes, which act on contractile cells. Vascular smooth muscle cells and pericytes are the contractile cells associated with arterioles and capillaries, respectively, which relax and induce vasodilation. Much progress has been made in understanding the complex signalling pathways of neurovascular coupling, but issues such as the contributions of capillary pericytes and astrocyte calcium signal remain contentious. Study of neurovascular coupling mechanisms is especially important as cerebral blood flow dysregulation is a prominent feature of Alzheimer’s disease. In this article we will discuss developments and controversies in the understanding of neurovascular coupling and finish by discussing current knowledge concerning neurovascular uncoupling in Alzheimer’s disease.

Funder

National Health and Medical Research Council Australia

NIHR Biomedical Research Centre

UK MS Society

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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