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<edm:dataProvider>University of Veterinary Medicine Vienna</edm:dataProvider>

  
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<dc:title xml:lang="en">[11C]metoclopramide is a sensitive radiotracer to measure moderate decreases in P-glycoprotein function at the blood-brain barrier</dc:title>

  
<dc:description xml:lang="en">The efflux transporter P-glycoprotein (P-gp) at the blood-brain barrier limits the cerebral uptake of various xenobiotics. To assess the sensitivity of [11C]metoclopramide to measure decreased cerebral P-gp function, we performed [11C]metoclopramide PET scans without (baseline) and with partial P-gp inhibition by tariquidar in wild-type, heterozygous Abcb1a/b(+/−) and homozygous Abcb1a/b(−/−) mice as models with controlled levels of cerebral P-gp expression. Brains were collected to quantify P-gp expression with immunohistochemistry. Brain uptake of [11C]metoclopramide was expressed as the area under the brain time-activity curve (AUCbrain) and compared with data previously obtained with (R)-[11C]verapamil and [11C]N-desmethyl-loperamide. Abcb1a/b(+/−) mice had intermediate P-gp expression compared to wild-type and Abcb1a/b(−/−) mice. In baseline scans, all three radiotracers were able to discriminate Abcb1a/b(−/−) from wild-type mice (2.5- to 4.6-fold increased AUCbrain, p ≤ 0.0001). However, only [11C]metoclopramide could discriminate Abcb1a/b(+/−) from wild-type mice (1.46-fold increased AUCbrain, p ≤ 0.001). After partial P-gp inhibition, differences in [11C]metoclopramide AUCbrain between Abcb1a/b(+/−) and wild-type mice (1.39-fold, p ≤ 0.001) remained comparable to baseline. There was a negative correlation between baseline [11C]metoclopramide AUCbrain and ex-vivo-measured P-gp immunofluorescence (r = −0.9875, p ≤ 0.0001). Our data suggest that [11C]metoclopramide is a sensitive radiotracer to measure moderate, but (patho-)physiologically relevant decreases in cerebral P-gp function without the need to co-administer a P-gp inhibitor.</dc:description>

  
<dc:identifier rdf:resource="https://phaidra.vetmeduni.ac.at/o:4452"></dc:identifier>

  
<dc:language>en</dc:language>

  
<edm:type>TEXT</edm:type>

  
<dc:type>journal article</dc:type>

  
<dc:type>Wissenschaftlicher Artikel</dc:type>

  
<dc:type>Articolo di rivista</dc:type>

  
<dc:type xml:lang="de">Text</dc:type>

  
<dc:type xml:lang="de">Wissenschaftlicher Artikel</dc:type>

  
<dc:type xml:lang="en">Text</dc:type>

  
<dc:type xml:lang="en">journal article</dc:type>

  
<dc:type xml:lang="it">Testo</dc:type>

  
<dc:type xml:lang="it">Articolo di rivista</dc:type>

  
<dc:subject xml:lang="en">P-Glycoprotein</dc:subject>

  
<dc:subject xml:lang="en">Blood-Brain Barrier</dc:subject>

  
<dc:subject xml:lang="en">PET</dc:subject>

  
<dc:subject xml:lang="en">[11C]metoclopramide</dc:subject>

  
<dc:subject xml:lang="en">Heterozygous Abcb1a/b Knockout Mice</dc:subject>

  
<dcterms:issued>2024</dcterms:issued>

  
<dc:date>2024</dc:date>

  
<dc:creator>Severin Mairinger</dc:creator>

  
<dc:creator>S. Leterrier</dc:creator>

  
<dc:creator>Thomas Filip</dc:creator>

  
<dc:creator>Mathilde Loebsch</dc:creator>

  
<dc:creator>Jens Pahnke</dc:creator>

  
<dc:creator>Irene Hernández-Lozano</dc:creator>

  
<dc:creator>J. Stanek</dc:creator>

  
<dc:creator>Nicolas Tournier</dc:creator>

  
<dc:creator>Markus Zeitlinger</dc:creator>

  
<dc:creator>Marcus Hacker</dc:creator>

  
<dc:creator>Oliver Langer</dc:creator>

  
<dc:creator>Thomas Wanek</dc:creator>

  
<dc:publisher>Sage</dc:publisher>

  
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