Influence of P-glycoprotein modulation on plasma concentrations and pharmacokinetics of orally administered prednisolone in dogs
- Author
- Sara Van der Heyden (UGent) , Siska Croubels (UGent) , Caroline Gadeyne (UGent) , Richard Ducatelle (UGent) , Sylvie Daminet (UGent) , Hugo Murua Escobar, Katharina Sterenczak, Ingeborgh Polis (UGent) , Stijn Schauvliege (UGent) , Myriam Hesta (UGent) and Koen Chiers (UGent)
- Organization
-
- Department of Large Animal Surgery, Anaesthesia and Orthopaedics
- Department of Small animals
- Department of Pharmacology, Toxicology and Biochemistry (ceased 1-1-2022)
- Department of Pathology, bacteriology and poultry diseases (ceased 1-1-2022)
- Department of Nutrition, Genetics and Ethology (ceased 1-1-2022)
- Abstract
- Objective-To evaluate the impact of modulation of the membrane-bound efflux pump P-glycoprotein (P-gp) on plasma concentrations of orally administered prednisolone in dogs. Animals-7 healthy adult Beagles. Procedures-Each dog received 3 treatments (control [no treatment], rifampicin [100 mg/d, PO, for 21 days, as an inducer of P-gp], and ketoconazole [100 mg/d, PO, for 21 days, as an inhibitor of P-gp]). A single dose of prednisolone (1 mg/kg, PO) was administered on day 8 of each treatment period. There was a 7-day washout period between subsequent treatments. Plasma concentrations of prednisolone were determined by use of a validated liquid chromatography-tandem mass spectrometry method. Duodenum and colon biopsy specimens were obtained endoscopically from anesthetized dogs and assessed for P-gp protein labeling via immunohistochemical analysis and mRNA quantification via real-time PCR assay. Total fecal collection was performed for evaluation of effects of P-gp modulation on digestion of nutrients. Results-Rifampicin treatment upregulated duodenal P-gp in dogs and significantly reduced the area under the plasma concentration-time curve of prednisolone. Ketoconazole typically downregulated expression of duodenal P-gp, with a subsequent increase in the area under the plasma concentration-time curve of prednisolone. There was a noticeable interindividual difference in response. Digestion of nutrients was not affected. Conclusions and Clinical Relevance-Modulation of P-gp expression influenced plasma concentrations of prednisolone after oral administration in dogs. Thus, treatment response to prednisolone may be influenced by coadministration of P-gp-modulating medications or feed ingredients.
- Keywords
- EFFLUX TRANSPORTERS, COMBINATION CHEMOTHERAPY, CYTOCHROME-P450 3A, HUMAN-TISSUES, BEAGLE DOGS, KETOCONAZOLE, CYCLOSPORINE, ABSORPTION, EXPRESSION, INHIBITION
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-3124467
- MLA
- Van der Heyden, Sara, et al. “Influence of P-Glycoprotein Modulation on Plasma Concentrations and Pharmacokinetics of Orally Administered Prednisolone in Dogs.” AMERICAN JOURNAL OF VETERINARY RESEARCH, vol. 73, no. 6, 2012, pp. 900–07, doi:10.2460/ajvr.73.6.900.
- APA
- Van der Heyden, S., Croubels, S., Gadeyne, C., Ducatelle, R., Daminet, S., Murua Escobar, H., … Chiers, K. (2012). Influence of P-glycoprotein modulation on plasma concentrations and pharmacokinetics of orally administered prednisolone in dogs. AMERICAN JOURNAL OF VETERINARY RESEARCH, 73(6), 900–907. https://doi.org/10.2460/ajvr.73.6.900
- Chicago author-date
- Van der Heyden, Sara, Siska Croubels, Caroline Gadeyne, Richard Ducatelle, Sylvie Daminet, Hugo Murua Escobar, Katharina Sterenczak, et al. 2012. “Influence of P-Glycoprotein Modulation on Plasma Concentrations and Pharmacokinetics of Orally Administered Prednisolone in Dogs.” AMERICAN JOURNAL OF VETERINARY RESEARCH 73 (6): 900–907. https://doi.org/10.2460/ajvr.73.6.900.
- Chicago author-date (all authors)
- Van der Heyden, Sara, Siska Croubels, Caroline Gadeyne, Richard Ducatelle, Sylvie Daminet, Hugo Murua Escobar, Katharina Sterenczak, Ingeborgh Polis, Stijn Schauvliege, Myriam Hesta, and Koen Chiers. 2012. “Influence of P-Glycoprotein Modulation on Plasma Concentrations and Pharmacokinetics of Orally Administered Prednisolone in Dogs.” AMERICAN JOURNAL OF VETERINARY RESEARCH 73 (6): 900–907. doi:10.2460/ajvr.73.6.900.
- Vancouver
- 1.Van der Heyden S, Croubels S, Gadeyne C, Ducatelle R, Daminet S, Murua Escobar H, et al. Influence of P-glycoprotein modulation on plasma concentrations and pharmacokinetics of orally administered prednisolone in dogs. AMERICAN JOURNAL OF VETERINARY RESEARCH. 2012;73(6):900–7.
- IEEE
- [1]S. Van der Heyden et al., “Influence of P-glycoprotein modulation on plasma concentrations and pharmacokinetics of orally administered prednisolone in dogs,” AMERICAN JOURNAL OF VETERINARY RESEARCH, vol. 73, no. 6, pp. 900–907, 2012.
@article{3124467, abstract = {{Objective-To evaluate the impact of modulation of the membrane-bound efflux pump P-glycoprotein (P-gp) on plasma concentrations of orally administered prednisolone in dogs. Animals-7 healthy adult Beagles. Procedures-Each dog received 3 treatments (control [no treatment], rifampicin [100 mg/d, PO, for 21 days, as an inducer of P-gp], and ketoconazole [100 mg/d, PO, for 21 days, as an inhibitor of P-gp]). A single dose of prednisolone (1 mg/kg, PO) was administered on day 8 of each treatment period. There was a 7-day washout period between subsequent treatments. Plasma concentrations of prednisolone were determined by use of a validated liquid chromatography-tandem mass spectrometry method. Duodenum and colon biopsy specimens were obtained endoscopically from anesthetized dogs and assessed for P-gp protein labeling via immunohistochemical analysis and mRNA quantification via real-time PCR assay. Total fecal collection was performed for evaluation of effects of P-gp modulation on digestion of nutrients. Results-Rifampicin treatment upregulated duodenal P-gp in dogs and significantly reduced the area under the plasma concentration-time curve of prednisolone. Ketoconazole typically downregulated expression of duodenal P-gp, with a subsequent increase in the area under the plasma concentration-time curve of prednisolone. There was a noticeable interindividual difference in response. Digestion of nutrients was not affected. Conclusions and Clinical Relevance-Modulation of P-gp expression influenced plasma concentrations of prednisolone after oral administration in dogs. Thus, treatment response to prednisolone may be influenced by coadministration of P-gp-modulating medications or feed ingredients.}}, author = {{Van der Heyden, Sara and Croubels, Siska and Gadeyne, Caroline and Ducatelle, Richard and Daminet, Sylvie and Murua Escobar, Hugo and Sterenczak, Katharina and Polis, Ingeborgh and Schauvliege, Stijn and Hesta, Myriam and Chiers, Koen}}, issn = {{0002-9645}}, journal = {{AMERICAN JOURNAL OF VETERINARY RESEARCH}}, keywords = {{EFFLUX TRANSPORTERS,COMBINATION CHEMOTHERAPY,CYTOCHROME-P450 3A,HUMAN-TISSUES,BEAGLE DOGS,KETOCONAZOLE,CYCLOSPORINE,ABSORPTION,EXPRESSION,INHIBITION}}, language = {{eng}}, number = {{6}}, pages = {{900--907}}, title = {{Influence of P-glycoprotein modulation on plasma concentrations and pharmacokinetics of orally administered prednisolone in dogs}}, url = {{http://doi.org/10.2460/ajvr.73.6.900}}, volume = {{73}}, year = {{2012}}, }
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