Effect of inhaled oxygen level on dynamic glucose‐enhanced MRI in mouse brain

Author:

Huang Jianpan1ORCID,Chen Zilin2,van Zijl Peter C. M.34,Hin Law Lok2,Pemmasani Prabakaran Rohith Saai25,Park Se Weon25,Xu Jiadi34,Chan Kannie W. Y.24567ORCID

Affiliation:

1. Department of Diagnostic Radiology The University of Hong Kong Hong Kong China

2. Department of Biomedical Engineering City University of Hong Kong Hong Kong China

3. F.M. Kirby Research Center for Functional Brain Imaging Kennedy Krieger Research Institute Baltimore Maryland USA

4. Russell H. Morgan Department of Radiology and Radiological Science The Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Hong Kong Centre for Cerebro‐Cardiovascular Health Engineering (COCHE) Hong Kong China

6. City University of Hong Kong Shenzhen Research Institute Shenzhen China

7. Tung Biomedical Science Centre, City University of Hong Kong Hong Kong China

Abstract

AbstractPurposeTo investigate the effect of inhaled oxygen level on dynamic glucose enhanced (DGE) MRI in mouse brain tissue and CSF at 3 T.MethodsDGE data of brain tissue and CSF from mice under normoxia or hyperoxia were acquired in independent and interleaved experiments using on‐resonance variable delay multi‐pulse (onVDMP) MRI. A bolus of 0.15 mL filtered 50% D‐glucose was injected through the tail vein over 1 min during DGE acquisition. MRS was acquired before and after DGE experiments to confirm the presence of D‐glucose.ResultsA significantly higher DGE effect under normoxia than under hyperoxia was observed in brain tissue (p = 0.0001 and p = 0.0002 for independent and interleaved experiments, respectively), but not in CSF (p > 0.3). This difference is attributed to the increased baseline MR tissue signal under hyperoxia induced by a shortened T1 and an increased BOLD effect. When switching from hyperoxia to normoxia without glucose injection, a signal change of ˜3.0% was found in brain tissue and a signal change of ˜1.5% was found in CSF.ConclusionsDGE signal was significantly lower under hyperoxia than that under normoxia in brain tissue, but not in CSF. The reason is that DGE effect size of brain tissue is affected by the baseline signal, which could be influenced by T1 change and BOLD effect. Therefore, DGE experiments in which the oxygenation level is changed from baseline need to be interpreted carefully.

Funder

University of Hong Kong

National Natural Science Foundation of China

City University of Hong Kong

National Institutes of Health

Research Grants Council, University Grants Committee

Publisher

Wiley

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