RT Journal Article
SR Electronic
T1 Blood-Brain Barrier (BBB) Pharmacoproteomics: Reconstruction of In Vivo Brain Distribution of 11 P-Glycoprotein Substrates Based on the BBB Transporter Protein Concentration, In Vitro Intrinsic Transport Activity, and Unbound Fraction in Plasma and Brain in Mice
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 579
OP 588
DO 10.1124/jpet.111.184200
VO 339
IS 2
A1 Yasuo Uchida
A1 Sumio Ohtsuki
A1 Junichi Kamiie
A1 Tetsuya Terasaki
YR 2011
UL http://jpet.aspetjournals.org/content/339/2/579.abstract
AB The purpose of this study was to examine whether in vivo drug distribution to the brain can be reconstructed by integrating P-glycoprotein (P-gp)/mdr1a expression levels, P-gp in vitro activity, and drug unbound fractions in mouse plasma and brain. For 11 P-gp substrates, in vitro P-gp transport activities were determined by measuring transcellular transport across monolayers of mouse P-gp-transfected LLC-PK1 (L-mdr1a) and parental cells. P-gp expression amounts were determined by quantitative targeted absolute proteomics. Unbound drug fractions in plasma and brain were obtained from the literature and by measuring brain slice uptake, respectively. Brain-to-plasma concentration ratios (Kp brain) and its ratios between wild-type and mdr1a/1b(−/−) mice (Kp brain ratio) were obtained from the literature or determined by intravenous constant infusion. Unbound brain-to-plasma concentration ratios (Kp,uu,brain) were estimated from Kp brain and unbound fractions. Based on pharmacokinetic theory, Kp brain ratios were reconstructed from in vitro P-gp transport activities and P-gp expression amounts in L-mdr1a cells and mouse brain capillaries. All reconstructed Kp brain ratios were within a 1.6-fold range of observed values. Kp brain then was reconstructed from the reconstructed Kp brain ratios and unbound fractions. Kp,uu,brain was reconstructed as the reciprocal of the reconstructed Kp brain ratios. For quinidine, loperamide, risperidone, indinavir, dexamethasone, paclitaxel, verapamil, loratadine, and diazepam, the reconstructed Kp brain and Kp,uu,brain agreed with observed and estimated in vivo values within a 3-fold range, respectively. Thus, brain distributions of P-gp substrates can be reconstructed from P-gp expression levels, in vitro activity, and drug unbound fractions.