Head-to-head comparison of (R)-[C]verapamil and [F]MC225 in non-human primates, tracers for measuring P-glycoprotein function
Creators
- 1. Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen (Netherlands)
- 2. Department of Nuclear Medicine and Molecular Imaging Group, Clinical University Hospital, IDIS Health Research Institute, Santiago de Compostela (Spain)
- 3. Central Research Laboratory, Hamamatsu Photonics K. K, Hamamatsu (Japan)
- 4. Research Team for Neuroimaging, Tokyo Metropolitan Institute of Gerontology, Tokyo (Japan)
- 5. Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari, Bari (Italy)
Description
P-glycoprotein (P-gp) function is altered in several brain disorders; thus, it is of interest to monitor the P-gp function in vivo using PET. (R)-[C]verapamil is considered the gold standard tracer to measure the P-gp function; however, it presents some drawbacks that limit its use. New P-gp tracers have been developed with improved properties, such as [F]MC225. This study compares the characteristics of (R)-[C]verapamil and [F]MC225 in the same subjects. Three non-human primates underwent 4 PET scans: 2 with (R)-[C]verapamil and 2 with [F]MC225, at baseline and after P-gp inhibition. The 30-min PET data were analyzed using 1-Tissue Compartment Model (1-TCM) and metabolite-corrected plasma as input function. Tracer kinetic parameters at baseline and after inhibition were compared. Regional differences and simplified methods to quantify the P-gp function were also assessed. At baseline, [F]MC225 V values were higher, and k values were lower than those of (R)-[C]verapamil, whereas K values were not significantly different. After inhibition, V values of the 2 tracers were similar; however, (R)-[C]verapamil K and k values were higher than those of [F]MC225. Significant regional differences between tracers were found at baseline, which disappeared after inhibition. The positive slope of the SUV-TAC was positively correlated to the K and V of both tracers. [F]MC225 and (R)-[C]verapamil show comparable sensitivity to measure the P-gp function in non-human primates. Moreover, this study highlights the 30-min V as the best parameter to measure decreases in the P-gp function with both tracers. [F]MC225 may become the first radiofluorinated tracer able to measure decreases and increases in the P-gp function due to its higher baseline V.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-021-05411-2Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 48
- Journal Issue
- 13
- Journal Page Range
- p. 4307-4317
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 53015437
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BLOOD-BRAIN BARRIER; BRAIN; CARBON 11; COMPARATIVE EVALUATIONS; FLUORINE 18; GLYCOPROTEINS; IMAGE PROCESSING; MENTAL DISORDERS; METABOLITES; NERVOUS SYSTEM DISEASES; NMR IMAGING; PHARMACOLOGY; POSITRON COMPUTED TOMOGRAPHY; PRIMATES; RADIOPHARMACEUTICALS; RELAXATION TIME; SENSITIVITY; TRACER TECHNIQUES; WEIGHTING FUNCTIONS
- Descriptors DEC
- ANIMALS; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CARBOHYDRATES; CARBON ISOTOPES; CENTRAL NERVOUS SYSTEM; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; EVALUATION; EVEN-ODD NUCLEI; FLUORINE ISOTOPES; FUNCTIONS; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPE APPLICATIONS; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MAMMALS; MATERIALS; MINUTES LIVING RADIOISOTOPES; NANOSECONDS LIVING RADIOISOTOPES; NERVOUS SYSTEM; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PROCESSING; PROTEINS; RADIOACTIVE MATERIALS; RADIOISOTOPES; SACCHARIDES; TOMOGRAPHY; VERTEBRATES
Optional Information
- Notes
- Oncology #En Dash# Digestive tract