Water exchange rates measure active transport and homeostasis in neural tissue

Author:

Williamson Nathan H12ORCID,Ravin Rea13,Cai Teddy X14,Falgairolle Melanie56,O’Donovan Michael J5,Basser Peter J1

Affiliation:

1. National Institute of Child Health and Human Development, National Institutes of Health , Bethesda, MD 20892 , USA

2. National Institute of General Medical Sciences, National Institutes of Health , Bethesda, MD 20892 , USA

3. Celoptics , Rockville, MD 20850 , USA

4. Wellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford , Oxford OX3 9DU , UK

5. National Institute of Neurological Disorders and Stroke, National Institutes of Health , Bethesda, MD 20892 , USA

6. National Center for Complementary and Integrative Health, National Institutes of Health , Bethesda, MD 20892 , USA

Abstract

AbstractFor its size, the brain is the most metabolically active organ in the body. Most of its energy demand is used to maintain stable homeostatic physiological conditions. Altered homeostasis and active states are hallmarks of many diseases and disorders. Yet there is currently no direct and reliable method to assess homeostasis and absolute basal activity of cells in the tissue noninvasively without exogenous tracers or contrast agents. We propose a novel low-field, high-gradient diffusion exchange nuclear magnetic resonance (NMR) method capable of directly measuring cellular metabolic activity via the rate constant for water exchange across cell membranes. Exchange rates are 140±16 s−1 under normal conditions in viable ex vivo neonatal mouse spinal cords. High repeatability across samples suggest that values are absolute and intrinsic to the tissue. Using temperature and drug (ouabain) perturbations, we find that the majority of water exchange is metabolically active and coupled to active transport by the sodium–potassium pump. We show that this water exchange rate is sensitive primarily to tissue homeostasis and provides distinct functional information. In contrast, the apparent diffusion coefficient (ADC) measured with submillisecond diffusion times is sensitive primarily to tissue microstructure but not activity. Water exchange appears independently regulated from microstructural and oxygenation changes reported by ADC and T1 relaxation measurements in an oxygen–glucose deprivation model of stroke; exchange rates remain stable for 30–40 min before dropping to levels similar to the effect of ouabain and never completely recovering when oxygen and glucose are restored.

Publisher

Oxford University Press (OUP)

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