Detection of sex‐specific glutamate changes in subregions of hippocampus in an early‐stage Alzheimer's disease mouse model using GluCEST MRI

Author:

Soni Narayan Datt1,Swain Anshuman12,Juul Halvor1,Cao Quy3,Haris Mohammad1,Wolk David A.45,Lee Virginia M.‐Y.56,Detre John A.7,Nanga Ravi Prakash Reddy1,Reddy Ravinder1ORCID

Affiliation:

1. Department of Radiology, Perelman School of Medicine Center for Advanced Metabolic Imaging in Precision Medicine University of Pennsylvania Philadelphia Pennsylvania USA

2. Department of Bioengineering, School of Engineering and Applied Sciences University of Pennsylvania Philadelphia Pennsylvania USA

3. Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

4. Center for Cognitive Neuroscience University of Pennsylvania Philadelphia Pennsylvania USA

5. Alzheimer's Disease Research Center Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

6. Center for Neurodegenerative Disease Research Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

7. Department of Neurology, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

Abstract

AbstractINTRODUCTIONRegional glucose hypometabolism resulting in glutamate loss has been shown as one of the characteristics of Alzheimer's disease (AD). Because the impact of AD varies between the sexes, we utilized glutamate‐weighted chemical exchange saturation transfer (GluCEST) magnetic resonance imaging (MRI) for high‐resolution spatial mapping of cerebral glutamate and investigated subregional changes in a sex‐specific manner.METHODSEight‐month‐old male and female AD mice harboring mutant amyloid precursor protein (APPNLF/NL‐F: n = 36) and wild‐type (WT: n = 39) mice underwent GluCEST MRI, followed by proton magnetic resonance spectroscopy (1H‐MRS) in hippocampus and thalamus/hypothalamus using 9.4T preclinical MR scanner.RESULTSGluCEST measurements revealed significant (p ≤ 0.02) glutamate loss in the entorhinal cortex (% change ± standard error: 8.73 ± 2.12%), hippocampus (11.29 ± 2.41%), and hippocampal fimbriae (19.15 ± 2.95%) of male AD mice. A similar loss of hippocampal glutamate in male AD mice (11.22 ± 2.33%; p = 0.01) was also observed in 1H‐MRS.DISCUSSIONSGluCEST MRI detected glutamate reductions in the fimbria and entorhinal cortex of male AD mice, which was not reported previously. Resilience in female AD mice against these changes indicates an intact status of cerebral energy metabolism.HighlightsGlutamate levels were monitored in different brain regions of early‐stage Alzheimer's disease (AD) and wild‐type male and female mice using glutamate‐weighted chemical exchange saturation transfer (GluCEST) magnetic resonance imaging (MRI).Male AD mice exhibited significant glutamate loss in the hippocampus, entorhinal cortex, and the fimbriae of the hippocampus.Interestingly, female AD mice did not have any glutamate loss in any brain region and should be investigated further to find the probable cause.These findings demonstrate previously unreported sex‐specific glutamate changes in hippocampal sub‐regions using high‐resolution GluCEST MRI.

Publisher

Wiley

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