Comparison of the endothelial toxicity induced by short-term amiodarone and diazepam exposure in a human umbilical vein endothelial cell line (EVC304)

References

• Armbruster C, Robibaro B, Griesmacher A, Vorbach H. (2000). Endothelial cell compatibility of trovafloxacin and levofloxacin for intravenous use. J Antimicrob Chemother 45:533–5
   PubMed Web of Science ®Google Scholar
• Brott D, Gould S, Jones H, et al. (2005). Biomarker of drug-induced vascular injury. Toxicol Appl Pharmacol 207:441–5
   PubMedGoogle Scholar
• Cheng ML, Ho HY, Liang CM, et al. (2000). Cellular glucose-6-phosphate dehydrogenase (G6PD) status modulates the effects of nitric oxide (NO) on human foreskin fibroblasts. FEBS Lett 475:257–62
   PubMed Web of Science ®Google Scholar
• Decker T, Lohmann-Matthes ML. (1988). A quick and simple method for the quantitation of lactate dehydrogenase release in measurements of cellular cytotoxicity and tumor necrosis factor (TNF) activity. J Immunol Methods 115:61–9
   PubMed Web of Science ®Google Scholar
• Fang YZ, Yang S, Wu G. (2002). Free radicals, antioxidants and nutrition. Nutrition 18:872–9
   PubMed Web of Science ®Google Scholar
• Freshney RI. (1983). Culture of Animal Cells. New York, USA: Alan R. Liss, Inc
   Google Scholar
• Gao LP, Cheng ML, Chou HJ, et al. (2009). Ineffective GSH regeneration enhances G6PD-knockdown hep G2 cell sensitivity to diamide-induced oxidative damage. Free Radic Biol Med 47:529–35
   PubMed Web of Science ®Google Scholar
• Hilleman DE, Hansen JM, Mohiuddin SM. (1987). Amiodarone-induced infusion phlebitis. Clin Pharm 6:364–67
   PubMedGoogle Scholar
• Hissin PJ, Hilf R. (1976). A fluorimetric method for determination of oxidized and reduced glutathione in tissues. Anal Biochem 74:214–26
   PubMed Web of Science ®Google Scholar
• Hoover DM, Gardner JB, Timmerman TL, et al. (1990). Comparison of in vitro and in vivo models to assess venous irritation of parenteral antibiotics. Fundam Appl Toxicol 4:589–97
   Google Scholar
• Hu G, Place AT, Minshall RD. (2008). Regulation of endothelial permeability by Src kinase signaling: Vascular leakage versus transcellular transport of drugs and macromolecules. Chem Biol Interact 171:177–89
   PubMed Web of Science ®Google Scholar
• Husa WJ, Adams JR. (1944). Isotonic solutions II. The permeability of red corpuscles to various substances. J Am Pharm Assoc Sci Ed 33:329–32
   Google Scholar
• Imamura H, Nhat KP, Togawa H, et al. (2009). Visualization of ATP levels inside single living cells with fluorescence resonance energy transfer-based genetically encoded indicators. Proc Natl Acad Sci USA 106:15651–6
   PubMed Web of Science ®Google Scholar
• Kohno E, Murase S, Nishikata M, et al. (2008). Methods of preventing vinorelbine-induced phlebitis: An experimental study in rabbits. Int J Med Sci 5:218–23
   PubMedGoogle Scholar
• Koizumi T, Shirakura H, Kumagai H, et al. (1996). Mechanism of cadmium-induced cytotoxicity in rat hepatocytes: Cadmium-induced active oxygen-related permeability changes of the plasma membrane. Toxicology 114:125–34
   PubMed Web of Science ®Google Scholar
• Kruse M, Kilic B, Flick B, Stahlmann R. (2007). Effect of quinupristin/dalfopristin on 3T3 and Eahy926 cells in vitro in comparison to other antimicrobial agents with the potential to induce infusion phlebitis. Arch Toxicol 81:447–52
   PubMed Web of Science ®Google Scholar
• Lee JW, Choi AH, Ham M, et al. (2011). G6PD up-regulation promotes pancreatic β-cell dysfunction. Endocrinology 152:793–803
   PubMed Web of Science ®Google Scholar
• Levy MY, Langerman L, Gottschalk-Sabag S, Benita S. (1989). Side-effect evaluation of a new diazepam formulation: Venous sequel reduction following intravenous (i.v.) injection of a diazepam emulsion in rabbits. Pharm Res 6:510–16
   PubMed Web of Science ®Google Scholar
• Masella R, Di Benedetto R, Varì R, et al. (2005). Novel mechanisms of natural antioxidant compounds in biological systems: Involvement of glutathione and glutathione-related enzymes. J Nutr Biochem 16:577–86
   PubMed Web of Science ®Google Scholar
• Medlicott NJ, Foster KA, Audus KL, et al. (1998). Comparison of the effects of potential parenteral vehicles for poorly water soluble anticancer drugs (organic cosolvents and cyclodextrin solutions) on cultured endothelial cells (HUV-EC). J Pharm Sci 87:1138–43
   PubMed Web of Science ®Google Scholar
• Mehta D, Malik AB. (2006). Signaling mechanisms regulating endothelial permeability. Physiol Rev 86:279–367
   PubMed Web of Science ®Google Scholar
• Millrose M, Kruse M, Flick B, Stahlmann R. (2009). Effects of macrolides on proinflammatory epitopes on endothelial cells in vitro. Arch Toxicol 83:469–76
   PubMed Web of Science ®Google Scholar
• Mutin M, Dignat-George F, Sampol J. (1997). Immunologic phenotype of cultured endothelial cells: Quantitative analysis of cell surface molecules. Tissue Antigens 50:449–58
   PubMedGoogle Scholar
• Nagai H, Matsumaru K, Feng G, Kaplowitz N. (2002). Reduced glutathione depletion causes necrosis and sensitization to tumor necrosis factor-alpha-induced apoptosis in cultured mouse hepatocytes. Hepatology 36:55–64
   PubMed Web of Science ®Google Scholar
• Paolucci-Jeanjean D, Belleville MP, Rios GM. (2001). A comprehensive study of the loss of enzyme activity in a continuous membrane reactor-application to starch hydrolysis. J Chem Technol Biotechnol 76:273–8
   Web of Science ®Google Scholar
• Parcell S. (2002). Sulfur in human nutrition and applications in medicine. Altern Med Rev 7:22–44
   PubMedGoogle Scholar
• Quillen EE, Haslam GC, Samra HS, et al. (2006). Ectoadenylate kinase and plasma membrane ATP synthase activities of human vascular endothelial cells. J Biol Chem 281:20728–37
   PubMed Web of Science ®Google Scholar
• Reed KW, Yalkowsky SH. (1985). Lysis of human red blood cells in the presence of various cosolvents. J Parenter Sci Technol 39:64–9
   PubMedGoogle Scholar
• Reed KW, Yalkowsky SH. (1986). Lysis of human red blood cells in the presence of various cosolvents. II. The effect of differing NaCl concentrations. J Parenter Sci Technol 40:88–94
   PubMedGoogle Scholar
• Robibaro B, Vorbach H, Weigel G, et al. (1998). Endothelial cell compatibility of glycopeptide antibiotics for intravenous use. J Antimicrob Chemother 41:297–300
   PubMed Web of Science ®Google Scholar
• Wang Y, Mesfin GM, Rodríguez CA, et al. (1999). Venous irritation, pharmacokinetics, and tissue distribution of tirilazad in rats following intravenous administration of a novel supersaturated submicron lipid emulsion. Pharm Res 16:930–8
   PubMed Web of Science ®Google Scholar
• Ward GH, Nolan PE Jr, White M, Yalkowsky SH. (1991a). Studies in phlebitis. II. Early detection of Amiodarone-induced phlebitis in a rabbit model. Pharm Res 8:801–3
   PubMed Web of Science ®Google Scholar
• Ward GH, Nolan PE Jr, Chawla M, Yalkowsky SH. (1991b). Studies in phlebitis: Detection and quantitation using a thermographic camera. Pharm Res 8:76–9
   PubMed Web of Science ®Google Scholar
• White M, Yalkowsky SH. (1991). Studies in phlebitis. III. Evaluation of diazapam and phenytoin. Pharm Res 8:1341–2
   PubMed Web of Science ®Google Scholar
• Yalkowsky SH. (1998). Solubility and Solubilization of Drugs. Washington, USA: American Chemical Society
   Google Scholar
• Yalkowsky SH, Krzyzaniak JF, Ward GH. (1998). Formulation-related problems associated with intravenous drug delivery. J Pharm Sci 87:787–96
   PubMed Web of Science ®Google Scholar
• Vorbach H, Weigel G, Robibaro B, et al. (1998). Endothelial cell compatibility of clarithromycin for intravenous use. Clin Biochem 31:653–6
   PubMed Web of Science ®Google Scholar
• Vorbach H, Robibaro B, Armbruster C, et al. (1999). Endothelial cell compatibility of clindamycin, gentamicin, ceftriaxone and teicoplanin in Bier's arterial arrest. J Antimicrob Chemother 44:275–7
   PubMed Web of Science ®Google Scholar
• Vorbach H, Armbruster C, Robibaro B, et al. (2002). Endothelial cell compatibility of azithromycin and erythromycin. J Antimicrob Chemother 49:407–9
   PubMed Web of Science ®Google Scholar