Abstract
The aim of this study was to demonstrate the potential of a wireless pixelated β+-sensitive intracerebral probe (PIXSIC) for in vivo positron emission tomographic (PET) radiopharmacology in awake and freely moving rodents. The binding of [11C]raclopride to D2 dopamine receptors was measured in anesthetized and awake rats following injection of the radiotracer. Competitive binding was assessed with a cold raclopride injection 20 minutes later. The device can accurately monitor binding of PET ligands in freely moving rodents with a high spatiotemporal resolution. Reproducible time-activity curves were obtained for pixels throughout the striatum and cerebellum. A significantly lower [11C]raclopride tracer-specific binding was observed in awake animals. These first results pave the way for PET tracer pharmacokinetics measurements in freely moving rodents.
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CITATION STYLE
Balasse, L., Maerk, J., Pain, F., Genoux, A., Fieux, S., Lefebvre, F., … Zimmer, L. (2015). PIXSIC: A wireless intracerebral radiosensitive probe in freely moving rats. Molecular Imaging, 14(8), 484–489. https://doi.org/10.2310/7290.2015.00020
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