Direct mapping of 19F in 19FDG-6P in brain tissue at subcellular resolution using soft X-ray fluorescence

• Published in: Journal of physics. Conference series 2013-10, Vol.463 (1)
• Main Authors: Poitry-Yamate, C, Gianoncelli, A, Kourousias, G, Kaulich, B, Lepore, M, Gruetter, R, Kiskinova, M
• Format: Article
• Language: English
• Subjects: Brain; Fluorine; Glucose; Mapping; Metabolism; Neurons; Physics; Positron emission; Soft x rays; Spatial resolution; Tomography; X ray imagery; X-ray fluorescence
• ISSN: 1742-6588; 1742-6596
• DOI: 10.1088/1742-6596/463/1/012003

Low energy x-ray fluorescence (LEXRF) detection was optimized for imaging cerebral glucose metabolism by mapping the fluorine LEXRF signal of 19F in 19FDG, trapped as intracellular 19F-deoxyglucose-6-phosphate (19FDG-6P) at 1μm spatial resolution from 3μm thick brain slices. 19FDG metabolism was evaluated in brain structures closely resembling the general cerebral cytoarchitecture following formalin fixation of brain slices and their inclusion in an epon matrix. 2-dimensional distribution maps of 19FDG-6P were placed in a cytoarchitectural and morphological context by simultaneous LEXRF mapping of N and O, and scanning transmission x-ray (STXM) imaging. A disproportionately high uptake and metabolism of glucose was found in neuropil relative to intracellular domains of the cell body of hypothalamic neurons, showing directly that neurons, like glial cells, also metabolize glucose. As 19F-deoxyglucose-6P is structurally identical to 18F-deoxyglucose-6P, LEXRF of subcellular 19F provides a link to in vivo 18FDG PET, forming a novel basis for understanding the physiological mechanisms underlying the 18FDG PET image, and the contribution of neurons and glia to the PET signal.