PT - JOURNAL ARTICLE AU - Kazuto Yasuda AU - Cynthia Cline AU - Yvonne S Lin AU - Rachel Scheib AU - Samit Ganguly AU - Ranjit Thirumaran AU - Amarjit S Chaudhry AU - Richard B. Kim AU - Erin G. Schuetz TI - In Vivo Imaging of Human MDR1 Transcription in the Brain and Spine of MDR1-Luciferase Reporter Mice AID - 10.1124/dmd.115.065078 DP - 2015 Jan 01 TA - Drug Metabolism and Disposition PG - dmd.115.065078 4099 - http://dmd.aspetjournals.org/content/early/2015/08/17/dmd.115.065078.short 4100 - http://dmd.aspetjournals.org/content/early/2015/08/17/dmd.115.065078.full AB - P-glycoprotein (the product of the MDR1 (ABCB1) gene) at the blood-brain barrier (BBB) limits CNS entry of many prescribed drugs, contributing to the poor success rate of CNS drug candidates. Modulating Pgp expression could improve drug delivery into the brain but assays to predict regulation of human BBB Pgp are lacking. We developed a transgenic mouse model to monitor human MDR1 transcription in the brain and spinal cord in vivo. A reporter construct consisting of ~10 kb of the human MDR1 promoter controlling the firefly luciferase gene was used to generate a transgenic mouse line [MDR1-luc]. Fluorescence In Situ Hybridization localized the MDR1-luc transgene on chromosome 3. Reporter gene expression was monitored with an in vivo imaging system following D-luciferin injection. Basal expression was detectable in the brain, and treatment with activators of CAR, PXR and the glucocorticoid receptor induced brain and spinal MDR1-luc transcription. Since D-luciferin is a substrate of ABCG2, the feasibility of improving D-luciferin brain accumulation (and luciferase signal) was tested by coadministering the dual ABCB1/ABCG2 inhibitor elacridar. The brain and spine MDR1-luc signal intensity was increased by elacridar treatment suggesting enhanced D-luciferin brain bioavailability. There was regional heterogeneity in MDR1 transcription (cortex > cerebellum) that coincided with higher mouse Pgp protein expression. We confirmed luciferase expression in brain vessel endothelial cells by ex vivo analysis of tissue luciferase protein expression. We conclude that the MDR1-luc mouse provides a unique in vivo system to visualize MDR1 CNS expression and regulation.