Determining Glucose Metabolism Kinetics Using 18F-FDG Micro-PET/CT

Summary

This study describes a protocol that uses ¹⁸F-FDG and positron emission tomography/computed tomography (PET/CT) imaging, together with kinetic modelling, to quantify the in vivo, real-time uptake of ¹⁸F-FDG into tissues.

Abstract

This paper describes the use of ¹⁸F-FDG and micro-PET/CT imaging to determine in vivo glucose metabolism kinetics in mice (and is transferable to rats). Impaired uptake and metabolism of glucose in multiple organ systems due to insulin resistance is a hallmark of type 2 diabetes. The ability of this technique to extract an image-derived input function from the vena cava using an iterative deconvolution method eliminates the requirement of the collection of arterial blood samples. Fitting of tissue and vena cava time activity curves to a two-tissue, three compartment model permits the estimation of kinetic micro-parameters related to the ¹⁸F-FDG uptake from the plasma to the intracellular space, the rate of transport from intracellular space to plasma and the rate of ¹⁸F-FDG phosphorylation. This methodology allows for multiple measures of glucose uptake and metabolism kinetics in the context of longitudinal studies and also provides insights into the efficacy of therapeutic interventions.

Introduction

The purpose of this study was to develop a positron emission tomography/computed tomography (PET/CT) based methodology to quantify the in vivo, real-time uptake of glucose from the blood stream into specific tissues in mice. This was achieved using ¹⁸F-labelled fluorodeoxyglucose (FDG) to measure glucose uptake and kinetic modelling to estimate the rates of ¹⁸F-FDG uptake from the plasma to the intracellular space, the rate of transport from intracellular space to plasma and the rate of ¹⁸F-FDG phosphorylation.

In rodents, ¹⁸F-FDG has been used in the pre-clinical assessment of numerous cancer treatments¹, studies of tumor progression² and tumor metabolism³ as well as imaging of brown fat depots⁴, neuroinflamation⁵ and brain metabolism⁶.

Traditional methods used to examine the tissue specific uptake of glucose in mice (and rats) generally involve treatment with 2-deoxyglucose radiolabeled with either ³H or ¹⁴C followed by euthanasia, tissue collection and measurement of radioactivity in each tissue⁷. The use of PET/CT allows for noninvasive determination of glucose uptake and metabolism in multiple organs and regions simultaneously in live animals. Additionally, as euthanasia is not a requirement, this technique is suitable for use in longitudinal studies.

Type 2 diabetes mellitus (T2DM) is characterized by disrupted glucose metabolism and hyperglycemia secondary to reduced tissue responsiveness to insulin (insulin resistance) and the inability of pancreatic -cells to produce adequate amounts of insulin⁸. Kinetic analysis of glucose uptake and metabolism can provide important insights into the mechanism of action and efficacy of therapeutic interventions as well as allow for advanced monitoring of disease progression.

Protocol

All procedures described in this study were approved by the Sydney Local Health District and University of Sydney Animal Ethics Committees and followed the NIH Guide for the care and use of laboratory animals, Eighth edition (2011).

1. Animal Preparation

NOTE: In this protocol male db/db mice (BKS.Cg-Dock7^m +/+ Lepr^db/J) were maintained in group housing with ad libitum access to chow and water until 6 weeks of age. At the time of imaging, mice weighed ~ 30 g. All mice used in this protocol had fasting blood glucose levels between 10 and 14 mmol/L.

1. If required, fast the mice. In the present example, fast the mice for 5 h prior to the experimental procedure.
2. Treat mice with the desired agent (e.g. drug, protein, peptide) before the commencement of imaging. In this example, administer a subcutaneous injection of insulin (3 U/kg human insulin) or equivalent volume PBS 30 min prior to the start of imaging.

2. Set up Workflow

NOTE: This protocol was implemented on a PET/CT scanner. Acquire PET data first, followed by acquisition of CT data.

1. PET settings:
   1. Select isotope as ¹⁸F, set scan duration to 3,600 s, and upper and lower level energy discrimination to 350 keV - 650 keV (default) with a coincidence timing window of 3.432 ns (default). Histogram list-mode data into 16 frames (6 × 10 s, 4 × 60 s, 1 × 300 s, 5 × 600 s) for the period 0 - 60 min after tracer injection. Reconstruct emission sinograms using 2D-FBP with a zoom 1.5.
      NOTE: The reconstructed images consisted of 16 dynamic frames, each with 128 × 128 × 159 voxels and a voxel size of 0.52 × 0.52 × 0.796 mm³.
2. CT settings:
   1. For a whole body CT scan, set the current at 500 A, voltage at 50 kV, exposure time 500 ms and 200 projections over a 360 rotation. Set the detector field of view (FoV) to 30722048, number of bed positions to 3 (to cover full PET FoV range), overlap between bed positions = 30.234713% and detector binning to 4.
      NOTE: CT reconstruction was performed using cone beam tomography image reconstruction software with HU calibration, bilinear interpolation and Shepp-Logan filter.
3. ¹⁸ F-FDG:
   1. Order sufficient ¹⁸F-FDG (for example 450 MBq in 0.5 mL) from a local provider to arrive ~ 30 min before the first injection. Aliquot and dilute the ¹⁸F-FDG so that animals receive ~ 10 MBq of ¹⁸F-FDG in a final volume of 0.1 mL.

3. Imaging Protocol

1. Wipe down induction chamber and imaging bed with 80% (v/v) ethanol to maintain aseptic conditions. Place the mouse in an induction chamber and anesthetize with 5% isoflurane in oxygen.
2. Place the mouse onto an imaging bed fitted with an electric heating pad to maintain body temperature and a precision vaporizer nose cone to deliver isoflurane (maintenance, 1.5 - 2%) at a flow rate of 1 L/min. Apply ophthalmic ointment onto eyes to prevent dryness whilst under anesthesia.
3. Position the mouse in a prone position on a sensor pad to monitor breathing and ensure an adequate plane of anesthesia is maintained.
4. Warm the tail using a heat pack for 1 - 2 min to dilate the lateral tail vein. Catheterize the lateral tail vein by inserting a 30-gauge needle into the lateral tail vein. Secure the needle in place with surgical glue and secure the catheter.
5. Load imaging bed into the scanner and move the bed through the machine so that the catheter can be accessed from the rear of the machine.
6. Attach the catheter to the ¹⁸F-FDG syringe in a syringe driver. Calculate the exact ¹⁸F-FDG dose (10 MBq) based on activity in syringe before injection and the volume to be administered (< 100 μL, injected over 10 s).
7. To minimize the impact of anesthesia on variability of glucose uptake, ensure a constant time between induction of anesthesia and injection of ¹⁸F-FDG (for example, 30 min).
8. Commence the PET scan immediately before injection of ¹⁸F-FDG. After finishing the PET scan (3,600 s), perform a CT scan (~ 10 min) to allow for co-registration of radiotracer uptake with tissues.
9. Move the imaging bed to the starting position, remove the animal from the bed.
10. At this point euthanize the animal or allow it to recover:
    1. For euthanasia, perform cervical dislocation whilst still under anesthesia and collect organs of interest for subsequent analysis.
    2. If allowing the mouse to recover, place the mouse in single housing on a heating pad or in front of a heating lamp. Monitor the mouse until it has regained sufficient consciousness to maintain sternal recumbency. Allow the mouse to recover for 1 h before returning to group housing.

4. PET Image Processing

NOTE: Image reconstruction was performed using acquisition workplace software v1.5.0.28 and analysis in research workplace software v4.2.

1. Co-register CT and PET images and ensure that the alignment is correct in all 3 dimensions.
   1. In the 'File' menu, select 'Folder Search/Import' and select the folder containing the data. Select the desired PET and CT data and click on the 'General Analysis' tab.
   2. Sort the data so that the CR is designated 'Source' and PET is designated 'Target'. In the 'Workflow' menu, select 'Registration'. If the images require adjustment to be correctly co-registered, use the tools in the 'Registration' menu.
2. In the 'Workflow' menu, select 'ROI Quantification'.
   1. Use the 'Pan' and 'Zoom' functions in the 'Image' tab to locate the desired region. In the 'Tools' menu, select the 'Create' tab and click the paintbrush icon. Draw the ROI on the image
3. Extract time-activity curves by selecting 'Save ROI Quantification' from the 'Save' menu. Save the data as a CSV file.
4. Quantify radioactivity uptake as Bq per cm³ of tissue. Convert values into percentage of injected dose per cm³ (% ID/ cm³) by loading the CSV file into a spreadsheet.

5. Input Function

1. To correct for the system point spread function, deconvolve the estimated system PSF for 5 iterations using the reblurred Van Cittert deconvolution method as previously described⁹.
   NOTE: This is required due to the small size of the vena cava in a mouse.
2. Use post deconvolution images to generate a blood input function time-activity curve as described above.

6. Kinetic Modeling

NOTE: The FDG two-tissue compartment model (Figure 1) requires the plasma input function.

1. Convert the blood input function in the CSV file to the plasma input function using the following equation¹⁰: Input_plasma = Input_blood × (0.386e^−0.191t + 1.165).
2. In the kinetic modelling tool click the 'Kinetic' button. Import the tissue and plasma total activity count CSV files into the kinetic modelling tool by selecting 'Load Time Activity Curve' from the 'Menu'.
3. In the 'Model' menu select 2 tissue compartments. Ensure that the box next to k4 is unselected and enter a value of 0. For initial fitting, uncheck the box for vB (blood volume fraction) and enter a value of 2%.
4. Click the 'Fit current region'. Correct the extracted region of interest for dispersion^11,12. Achieve this by minimizing the Chi-square value for the FDG model for different dispersion times.
5. Perform a second fit using floating vB value (check the box next to the box for vB) and the optimized dispersion value to calculate the regional rate constants (k₁-k₃). Calculate the regional influx constant as K_i = (k₁ × k₃) / (k₂ + k₃).

Results

We have previously used the db/db mouse model to investigate the impact of increasing plasma apoA-I levels on the kinetics of glucose uptake and metabolism¹³. In this study we used db/db mice treated with insulin to demonstrate the utility of PET/CT imaging to monitor the uptake of ¹⁸F-FDG from the plasma into the gastrocnemius muscle in real time.

Six week old db/db mice were anesthetized and ...

Discussion

The protocol described here represents a robust, non-invasive methodology to determine the kinetics of glucose uptake from the blood stream into tissue and subsequent metabolism in mice.

The db/db mouse is a is a well-established animal model of type 2 diabetes¹⁴ that has been used extensively to examine insulin resistance and relevant interventions. However, previous studies have only quantified endpoint uptake in the heart¹⁵ and cardiac and ske...

Materials

Name	Company	Catalog Number	Comments
PET/CT Scanner	Siemens	Inveon
18F-FDG	PETNET Solutions
Isoflurane	Pharmachem
30 guage needle	BD	305106
PMOD modelling software	PMOD Technologies
BKS.Cg-Dock7m +/+ Leprdb/J mice	Jackson Laboratory	000642
Human insulin	Sigma-Aldrich