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Inveon multimodality preclinical scanner

Manufactured by Siemens
Sourced in Germany

The Inveon multimodality preclinical scanner is a medical imaging device designed for small animal research. It combines multiple imaging modalities, including positron emission tomography (PET), single-photon emission computed tomography (SPECT), and computed tomography (CT), to provide comprehensive imaging capabilities for preclinical studies.

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2 protocols using inveon multimodality preclinical scanner

1

PET-CT Imaging of Ketamine Effects

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In a separate experiment, animals were randomly assigned into three groups: saline control (n = 11), 10 mg/kg (n = 9), or 20 mg/kg (n = 12) ketamine. Two 18F-FDG-PET and computed tomography (CT) scans were obtained for each animal at baseline, 4 to 5 days before the experiment (scan 1) and immediately after fear conditioning and ketamine infusion (scan 2). 18F-FDG-PET and CT images were acquired using an Inveon multimodality preclinical scanner (Siemens Medical Solutions, Erlangen, Germany) in the small animal imaging facility at USU as described previously [13 (link)]. Animals were briefly anesthetized with isoflurane (4% induction and 1.5–2.5% maintenance) and injected with 1.7 ± 0.153 mCi (62.9 ± 5.7 MBq) 18F-FDG through the tail vein. After 18F-FDG injection, the animal was returned to a clean cage during the uptake period (30 min) in a quiet room adjacent to the PET and CT scanner. Animals were undisturbed and exhibited minimal movement in their cages during the 18F-FDG uptake period. After uptake, animals were anesthetized with isoflurane (4% induction and 1.5 to 2.5% maintenance) to perform PET and CT scans. Physiologic monitoring during the scan included measurements of temperature, respiration rate, heart rate, and oxygen saturation.
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2

Insulin-Regulated Glucose Uptake in Mice

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Small-animal PET/CT was performed on a Siemens INVEON multimodality preclinical scanner. Mice (Dlk1+/+ n = 15, Dlk1−/− n = 13) were fasted overnight prior to PET/CT scanning at baseline (day 0) and one day later (day 1). Mice were subcutaneously injected with 75 μl saline or 0.75 U/(Kg body weight) short acting insulin (Humulin, NOVO Nordisk, DK) respectively, 15 min. Before injection of 18F-Fluoro-deoxy-glucose (FDG). Mice were anesthetized (2% isoflurane), and a bolus injection of FDG (day 0 95.5 ± 9.1 MBq; day 1: 91.6 ± 13.4 MBq) was administered via a tail vein catheter. Prior to the PET scan a two-bed CT scan was performed for attenuation correction of the PET data and anatomic orientation. CT and PET images were co-registered using a transformation matrix and CT-based attenuation correction was applied to the PET data. The PET data were reconstructed using the Siemens INVEON pre-clinical software and data analysis of the PET/CT fused images was performed with INVEON software version 4.2 (IRW, Siemens). FDG uptake in each volume of interest (VOI) was reported as standardized uptake values (SUV). VOIs of the skeletal limb hind muscles were normalized using brain uptake as a reference tissue that metabolizes glucose independent of insulin.
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