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Parametric Imaging of P-Glycoprotein Function at the Blood–Brain Barrier Using kE,brain-maps Generated from [11C]Metoclopramide PET Data in Rats, Nonhuman Primates and Humans.

Authors :
Breuil, Louise
El Biali, Myriam
Vodovar, Dominique
Marie, Solène
Auvity, Sylvain
Bauer, Martin
Goutal, Sébastien
Rodrigo, Sebastian
Langer, Oliver
Tournier, Nicolas
Source :
Molecular Imaging & Biology; Dec2023, Vol. 25 Issue 6, p1135-1141, 7p
Publication Year :
2023

Abstract

Purpose: PET imaging using [<superscript>11</superscript>C]metoclopramide revealed the importance of P-glycoprotein (P-gp, ABCB1) in mediating the brain-to-blood efflux of substrates across the blood–brain barrier (BBB). In this work, the elimination rate constant from the brain (k<subscript>E,brain</subscript>), calculated from dynamic PET images without the need for arterial blood sampling, was evaluated as an outcome parameter for the interpretation of [<superscript>11</superscript>C]metoclopramide PET data. Procedures: k<subscript>E,brain</subscript> parameter was obtained by linear regression of log-transformed brain time-activity curves (TACs). k<subscript>E,brain</subscript> values (h<superscript>−1</superscript>) obtained under baseline conditions were compared with values obtained after complete P-gp inhibition using tariquidar in rats (n = 4) and baboons (n = 4) or after partial inhibition using cyclosporine A in humans (n = 10). In baboons, the sensitivity of k<subscript>E,brain</subscript> to measure complete P-gp inhibition was compared with outcome parameters derived from kinetic modeling using a 1-tissue compartment model (1-TCM). Finally, k<subscript>E,brain</subscript>-maps were generated in each species using PMOD software. Results: The linear part of the log-transformed brain TACs occurred from 10 to 30 min after radiotracer injection in rats, from 15 to 60 min in baboons, and from 20 to 60 min in humans. P-gp inhibition significantly decreased k<subscript>E,brain</subscript> values by 39 ± 12% in rats (p < 0.01), by 32 ± 6% in baboons (p < 0.001), and by 37 ± 22% in humans (p < 0.001). In baboons, P-gp inhibition consistently decreased the brain-to-plasma efflux rate constant k<subscript>2</subscript> (36 ± 9%, p < 0.01) leading to an increase in the total brain volume of distribution (V<subscript>T</subscript>, 101 ± 12%, p < 0.001). In all studied species, brain k<subscript>E,brain</subscript>-maps displayed decreased P-gp-mediated efflux across the BBB. Conclusions: k<subscript>E,brain</subscript> of [<superscript>11</superscript>C]metoclopramide provides a simple outcome parameter to describe P-gp function in the living brain when arterial input function data are unavailable, although less sensitive than V<subscript>T</subscript>. k<subscript>E,brain</subscript>-maps represent easy to compute parametric images reflecting the effect of P-gp on [<superscript>11</superscript>C]metoclopramide elimination from the brain. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15361632
Volume :
25
Issue :
6
Database :
Complementary Index
Journal :
Molecular Imaging & Biology
Publication Type :
Academic Journal
Accession number :
174299029
Full Text :
https://doi.org/10.1007/s11307-023-01864-z