Ivermectin excretion by isolated functionally intact brain endothelial capillaries

被引:35
作者
Nobmann, S [1 ]
Bauer, B [1 ]
Fricker, G [1 ]
机构
[1] Univ Heidelberg, Inst Pharmaceut Technol & Biopharm, D-69120 Heidelberg, Germany
关键词
ivermectin; brain; capillary; blood-brain barrier; p-glycoprotein multidrug resistance related protein; confocal microscopy; active transport;
D O I
10.1038/sj.bjp.0703762
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Functionally intact brain endothelial capillaries were isolated from porcine brain. p-Glycoprotein was localized at the lumenal membrane of intact capillaries by immunohistochemistry using a murine monoclonal antibody and a secondary FITC fluorescent labelled anti-mouse IgG. Western blot staining of p-glycoprotein in isolated endothelial cells confirmed the immunohistochemistry. 2 Excretion of the fluorescent labelled anthelmintic drug Ivermectin (BODIPY-Ivermectin) was studied in the isolated brain endothelial capillaries. Drug accumulation in the capillary lumen was visualized by fluorescence confocal laser scanning microscopy and was measured by image analysis. Secretion of BODIPY-Ivermectin into the capillary lumen exhibited characteristics of specific and energy-dependent transport. Steady state Iumenal fluorescence intensity averaged 1.6 times cellular fluorescence and was reduced 3-4 times below cellular levels when metabolism was inhibited by NaCN. 3 BODIPY-Ivermectin secretion was inhibited in a concentration-dependent manner by unlabeled Ivermectin. In addition, lumenal but not cellular fluorescence intensity was significantly decreased when capillaries were incubated with PSC-833, Cyclosporin A or Verapamil, all inhibitors of p-glycoprotein. Conversely, unlabelled Ivermectin reduced the p-glycoprotein (Pgp)-mediated secretion of a fluorescent derivative of Verapamil, (BODIPY-Verapamil). 4 BODIPY-Ivermectin secretion was not affected in the presence of Leucotriene C-4 (LTC4), a potent inhibitor of multidrug resistance related protein (mrp)-mediated transport processes. In addition, excretion of Fluorescein-Methotrexate, an mrp-substrate, was not inhibited by Ivermectin. 5 Uptake experiments with isolated porcine brain capillary cells showing increased cellular uptake of BODIPY-Ivermectin in the presence of unlabelled drug or PSC-833 supported the findings of a Pgp interaction in intact capillaries. 6 The data are consistent with BODIPY-Ivermectin and Ivermectin being transported across the lumenal membrane of brain capillaries. For the first time Pgp-interaction of Ivermectin at the blood brain barrier is demonstrated on a cellular level in an intact vascular tissue.
引用
收藏
页码:722 / 728
页数:7
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