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- Title
Olanzapine Penetration into Brain is Greater in Transgenic Abcb P-glycoprotein-Deficient Mice than FVBI (Wild-Type) Animals.
- Authors
Jun-Sheng Wang; Taylor, Robin; Ying Ruan, Robin; Donovan, Jennifer L.; Markowitz, John S.; De Vane, C. Lindsay
- Abstract
The transmembrane energy-dependent efflux transporter P-glycoprotein (P-gp) limits a range of drugs from penetrating cells and deposits them into the extracellular space. P-gp is highly expressed in several normal tissues, including the luminal surface of capillary endothelial cells in the brain of humans. In this study, we tested whether olanzapine distribution to tissues highly expressing P-gp or devoid of this transporter was similar in Abcb 1a (-/-) mice lacking P-gp and control animals. At 1 h following the intraperitoneal injection of 2.5 µg olanzapine/g mouse, olanzapine concentrations were statistically and significantly higher in brain (three-fold), liver (2.6-fold), and kidney (1.8-fold) of Abcb 1a (-/-) mice than those of the control FVB Abcb 1a (+/+) mice, and not statistically different in plasma, spleen, or penile tissue. Similar differences were also found for the ratios of organ:plasma and organ:spleen between the two groups. This is the first report that the presence of the Abcb 1a gene is an important factor controlling brain access to olanzapine. The finding that the brain penetration of olanzapine is limited by P-gp implies that the highly prevalent functional polymorphisms of ABCB 1 in humans may be a factor contributing to variability in dose requirements for this antipsychotic drug.
- Subjects
OLANZAPINE; P-glycoprotein; ADENOSINE triphosphate; BLOOD-brain barrier; LABORATORY mice; NEUROPSYCHOPHARMACOLOGY
- Publication
Neuropsychopharmacology, 2004, Vol 29, Issue 3, p551
- ISSN
0893-133X
- Publication type
Article
- DOI
10.1038/sj.npp.1300372