TY - JOUR
T1 - Test-Retest Repeatability of [18F]MC225-PET in Rodents
T2 - A Tracer for Imaging of P-gp Function
AU - García-Varela, Lara
AU - Vállez García, David
AU - Rodríguez-Pérez, Manuel
AU - van Waarde, Aren
AU - Sijbesma, Jürgen W A
AU - Schildt, Anna
AU - Kwizera, Chantal
AU - Aguiar, Pablo
AU - Sobrino, Tomás
AU - Dierckx, Rudi A J O
AU - Elsinga, Philip H
AU - Luurtsema, Gert
PY - 2020/2/19
Y1 - 2020/2/19
N2 - In longitudinal PET studies, animals are repeatedly anesthetized which may affect the repeatability of PET measurements. The aim of this study was to assess the effect of anesthesia on the P-gp function as well as the reproducibility of [18F]MC225 PET scans. Thus, dynamic PET scans with blood sampling were conducted in 13 Wistar rats. Seven animals were exposed to isoflurane anesthesia 1 week before the PET scan ("Anesthesia-exposed" PET). A second group of six animals was used to evaluate the reproducibility of measurements of P-gp function at the blood-brain barrier (BBB) with [18F]MC225. In this group, two PET scans were made with a 1 week interval ("Test" and "Retest" PET). Pharmacokinetic parameters were calculated using compartmental models and metabolite-corrected plasma as an input function. "Anesthesia-exposed" animals showed a 28% decrease in whole-brain volume of distribution (VT) (p < 0.001) compared to "Test", where the animals were not previously anesthetized. The VT at "Retest" also decreased (19%) compared to "Test" (p < 0.001). The k2 values in whole-brain were significantly increased by 18% in "Anesthesia-exposed" (p = 0.005) and by 15% in "Retest" (p = 0.008) compared to "Test". However, no significant differences were found in the influx rate constant K1, which is considered as the best parameter to measure the P-gp function. Moreover, Western Blot analysis did not find significant differences in the P-gp expression of animals not pre-exposed to anesthesia ("Test") or pre-exposed animals ("Retest"). To conclude, anesthesia may affect the brain distribution of [18F]MC225 but it does not affect the P-gp expression or function.
AB - In longitudinal PET studies, animals are repeatedly anesthetized which may affect the repeatability of PET measurements. The aim of this study was to assess the effect of anesthesia on the P-gp function as well as the reproducibility of [18F]MC225 PET scans. Thus, dynamic PET scans with blood sampling were conducted in 13 Wistar rats. Seven animals were exposed to isoflurane anesthesia 1 week before the PET scan ("Anesthesia-exposed" PET). A second group of six animals was used to evaluate the reproducibility of measurements of P-gp function at the blood-brain barrier (BBB) with [18F]MC225. In this group, two PET scans were made with a 1 week interval ("Test" and "Retest" PET). Pharmacokinetic parameters were calculated using compartmental models and metabolite-corrected plasma as an input function. "Anesthesia-exposed" animals showed a 28% decrease in whole-brain volume of distribution (VT) (p < 0.001) compared to "Test", where the animals were not previously anesthetized. The VT at "Retest" also decreased (19%) compared to "Test" (p < 0.001). The k2 values in whole-brain were significantly increased by 18% in "Anesthesia-exposed" (p = 0.005) and by 15% in "Retest" (p = 0.008) compared to "Test". However, no significant differences were found in the influx rate constant K1, which is considered as the best parameter to measure the P-gp function. Moreover, Western Blot analysis did not find significant differences in the P-gp expression of animals not pre-exposed to anesthesia ("Test") or pre-exposed animals ("Retest"). To conclude, anesthesia may affect the brain distribution of [18F]MC225 but it does not affect the P-gp expression or function.
KW - ATP Binding Cassette Transporter, Subfamily B, Member 1/drug effects
KW - Animals
KW - Blood-Brain Barrier/drug effects
KW - Brain/drug effects
KW - Male
KW - Radionuclide Imaging
KW - Radiopharmaceuticals/pharmacology
KW - Rats, Wistar
KW - Reproducibility of Results
KW - Rodentia/metabolism
U2 - https://doi.org/10.1021/acschemneuro.9b00682
DO - https://doi.org/10.1021/acschemneuro.9b00682
M3 - Article
C2 - 31961646
SN - 1948-7193
VL - 11
SP - 648
EP - 658
JO - ACS Chemical Neuroscience
JF - ACS Chemical Neuroscience
IS - 4
ER -