Pregabalin Induces Hepatic Hypoxia and Increases EndothelialCell Proliferation in Mice, a Process Inhibited by DietaryVitamin E Supplementation
Autor: | Sharon A. Sokolowski, Steven Duddy, Kay A. Criswell, Zbigniew Wojcinski, Michael T. Lawton, Joseph T. Brady, Christopher Somps, Ramin Rahbari, Dennis C. Morse, Marc D. Roy, Jennifer Colangelo, Leslie A. Obert, Jon C. Cook, David G. Pegg, Petra H. Koza-Taylor, Timothy Anderson, Kimberly A. Navetta |
---|---|
Rok vydání: | 2012 |
Předmět: |
medicine.medical_specialty
Endothelium Liver cytology Basic fibroblast growth factor Pregabalin Toxicology Mice chemistry.chemical_compound Internal medicine Animals Vitamin E Medicine Platelet activation Chromatography High Pressure Liquid gamma-Aminobutyric Acid Cell Proliferation business.industry Hypoxia (medical) Cell Hypoxia Diet Endothelial stem cell Vascular endothelial growth factor Endocrinology medicine.anatomical_structure Liver chemistry Erythropoiesis Female Endothelium Vascular medicine.symptom business |
Zdroj: | Toxicological Sciences. 128:42-56 |
ISSN: | 1096-0929 1096-6080 |
DOI: | 10.1093/toxsci/kfs148 |
Popis: | The preceding article identified key components of pregabalin's mode of action on nongenotoxic hemangiosarcoma formation in mice, including increased serum bicarbonate leading to decreased respiratory rate, increased blood pH, increased venous oxygen saturation, increased vascular endothelial growth factor and basic fibroblast growth factor expression, increased hepatic vascular endothelial growth factor receptor 2 expression, and increased iron-laden macrophages. Increased platelet count and platelet activation were early, species-specific biomarkers in mice. Dysregulated erythropoiesis, macrophage activation, and elevations of tissue growth factors were consistent with the unified mode of action for nongenotoxic hemangiosarcoma recently proposed at an international hemangiosarcoma workshop (Cohen, S. M., Storer, R. D., Criswell, K. A., Doerrer, N. G., Dellarco, V. L., Pegg, D. G., Wojcinski, Z. W., Malarkey, D. E., Jacobs, A. C., Klaunig, J. E., et al. (2009). Hemangiosarcoma in rodents: Mode-of-action evaluation and human relevance. Toxicol. Sci. 111, 4-18). In this article, we present evidence that pregabalin induces hypoxia and increases endothelial cell (EC) proliferation in a species-specific manner. Dietary administration of pregabalin produced a significant 35% increase in an immunohistochemical stain for hypoxia (Hypoxyprobe) in livers from pregabalin-treated mice. Increased Hypoxyprobe staining was not observed in the liver, bone marrow, or spleen of rats, supporting the hypothesis that pregabalin produces local tissue hypoxia in a species-specific manner. Transcriptional analysis supports that rats, unlike mice, adapt to pregabalin-induced hypoxia. Using a dual-label method, increased EC proliferation was observed as early as 2 weeks in mouse liver and 12 weeks in bone marrow following pregabalin administration. These same assays showed decreased EC proliferation in hepatic ECs of rats, further supporting species specificity. Dietary supplementation with vitamin E, which is known to have antioxidant and antiangiogenic activity, inhibited pregabalin-induced increases in mouse hepatic EC proliferation, providing confirmatory evidence for the proposed mode of action and its species-specific response. |
Databáze: | OpenAIRE |
Externí odkaz: |