Expression and Localization of P-glycoprotein in Human Heart

Author:

Meissner Konrad12,Sperker Bernhard1,Karsten Christiane1,zu Schwabedissen Henriette Meyer1,Seeland Ute3,Böhm Michael23,Bien Sandra1,Dazert Peter1,Kunert-Keil Christiane1,Vogelgesang Silke4,Warzok Rolf4,Siegmund Werner1,Cascorbi Ingolf1,Wendt Michael2,Kroemer Heyo K.1

Affiliation:

1. Institut für Pharmakologie and Peter Holtz Research Center of Pharmacology and Experimental Therapeutics, Greifswald, Germany

2. Klinik für Anästhesiologie, Greifswald, Germany

3. Medizinische Klinik III, Universität des Saarlandes, Homburg/S., Germany

4. Institut für Pathologie, Ernst-Moritz-Arndt-Universität Greifswald, Greifswald, Germany

Abstract

ABC-type transport proteins, such as P-glycoprotein (P-gp), modify intracellular concentrations of many substrate compounds. They serve as functional barriers against entry of xenobiotics (e.g., in the gut or the blood-brain barrier) or contribute to drug excretion. Expression of transport proteins in the heart could be an important factor modifying cardiac concentrations of drugs known to be transported by P-gp (e.g., β-blockers, cardiac glycosides, doxorubicin). We therefore investigated the expression and localization of P-gp in human heart. Samples from 15 human hearts (left ventricle; five non-failing, five dilated cardiomyopathy, and five ischemic cardiomyopathy) were analyzed for expression of P-gp using real-time RT-PCR, immunohistochemistry, and in situ hybridization. Immunohistochemistry revealed expression of P-gp in endothelium of both arterioles and capillaries of all heart samples. Although P-gp mRNA was detected in all samples, its expression level was significantly reduced in patients with dilated cardiomyopathy. We describe variable expression of P-gp in human heart and its localization in the endothelial wall. Thus, intracardiac concentrations of various compounds may be modified, depending on the individual P-gp level.

Publisher

SAGE Publications

Subject

Histology,Anatomy

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