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Image-Derived Input Functions for Quantification of A1 Adenosine Receptors Availability in Mice Brains Using PET and [18F]CPFPX
Author(s) -
Xuan He,
Franziska Wedekind,
Tina Kroll,
Angela Oskamp,
Simone Beer,
Alexander Drzezga,
Johannes Ermert,
Bernd Neumaier,
Andreas Bauer,
David Elmenhorst
Publication year - 2020
Publication title -
frontiers in physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.32
H-Index - 102
ISSN - 1664-042X
DOI - 10.3389/fphys.2019.01617
Subject(s) - adenosine , receptor , neuroscience , adenosine receptor , biology , microbiology and biotechnology , computational biology , chemistry , computer science , endocrinology , biochemistry , agonist
Purpose In vivo imaging for the A 1 adenosine receptors (A 1 ARs) with positron emission tomography (PET) using 8-cyclopentyl-3-(3-[ 18 F]fluoropropyl)-1-propylxan- thine ([ 18 F]CPFPX) has become an important tool for studying physiological processes quantitatively in mice. However, the measurement of arterial input functions (AIFs) on mice is a method with restricted applicability because of the small total blood volume and the related difficulties in withdrawing blood. Therefore, the aim of this study was to extract an appropriate [ 18 F]CPFPX image-derived input function (IDIF) from dynamic PET images of mice. Procedures In this study, five mice were scanned with [ 18 F]CPFPX for 60 min. Arterial blood samples ( n = 7 per animal) were collected from the femoral artery and corrected for metabolites. To generate IDIFs, three different approaches were selected: (A) volume of interest (VOI) placed over the heart (cube, 10 mm); (B) VOI set over abdominal vena cava/aorta region with a cuboid (5 × 5 × 15 mm); and (C) with 1 × 1 × 1 mm voxels on five consecutive slices. A calculated scaling factor (α) was used to correct for partial volume effect; the method of obtaining the total metabolite correction of [ 18 F]CPFPX for IDIFs was developed. Three IDIFs were validated by comparison with AIF. Validation included the following: visual performance; computing area under the curve (AUC) ratios (IDIF/AIF) of whole-blood curves and parent curves; and the mean distribution volume ( V T ) ratios (IDIF/AIF) of A 1 ARs calculated by Logan plot and two-tissue compartment model. Results Compared with the AIF, the IDIF with VOI over heart showed the best performance among the three IDIFs after scaling by 1.77 (α) in terms of visual analysis, AUC ratios (IDIF/AIF; whole-blood AUC ratio, 1.03 ± 0.06; parent curve AUC ratio, 1.01 ± 0.10) and V T ratios (IDIF/AIF; Logan V T ratio, 1.00 ± 0.17; two-tissue compartment model V T ratio, 1.00 ± 0.13) evaluation. The A 1 ARs distribution of average parametric images was in good accordance to autoradiography of the mouse brain. Conclusion The proposed study provides evidence that IDIF with VOI over heart can replace AIF effectively for quantification of A 1 ARs using PET and [ 18 F]CPFPX in mice brains.

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