Nephrotoxic Potential and Toxicokinetics of Tetrabromobisphenol a in Rat for Risk Assessment

• Published in: Journal of Toxicology and Environmental Health, Part A Part A, 2009-11, Vol.72 (21-22), p.1439-1445
• Main Authors: Kang, Mi Jeong, Kim, Ju Hyun, Shin, Sil, Choi, Jae Ho, Lee, Sang Kyu, Kim, Hyung Sik, Kim, Nam Deuk, Kang, Geon Wook, Jeong, Hye Gwang, Kang, Wonku, Chun, Young Jin, Jeong, Tae Cheon
• Format: Article
• Language: English
• Subjects: Animals; Area Under Curve; Biochemistry; Bromination; Catalase; Chromatography; Dose-Response Relationship, Drug; Electric potential; Electronic equipment; Elevated; Feces; Fires; Flame retardants; Flame Retardants - administration & dosage; Flame Retardants - toxicity; Half-Life; Kidney Diseases - chemically induced; Kidneys; Laminates; Liquids; Male; Molecular Structure; Pharmacokinetics; Polybrominated Biphenyls - administration & dosage; Polybrominated Biphenyls - chemistry; Polybrominated Biphenyls - toxicity; Rats; Rats, Sprague-Dawley; Risk assessment; Safety; Serums; Sod; Specific Pathogen-Free Organisms; Spectroscopy; Tetrabromobisphenol A; Toxic; Toxicity; Toxicology; Urine
• ISSN: 1528-7394; 1087-2620
• DOI: 10.1080/15287390903212907

Tetrabromobisphenol A (TBBPA), one of the most widely used global brominated flame retardants, is used to improve fire safety of laminates in electrical and electronic equipment. To investigate the nephrotoxic potential of TBBPA and its toxicokinetic profile in rats, single-dose and daily 14-d repeated-dose toxicity studies at 200, 500, or 1000 mg/kg were performed. Several biochemical parameters were analyzed to evaluate nephrotoxicity of TBBPA. High-dose 1000 mg/kg TBBPA significantly elevated renal thiobarbituric acid-reactive substance (TBARS) levels, and superoxide dismutase (SOD) activity was increased at all 3 doses administered. This was associated with no change in the activity of catalase (CAT). Our results suggest that acute 1-d high-dose administration of TBBPA produced transient renal changes at 5 h. Subsequently, TBBPA in serum, urine, and kidney was determined by liquid chromatography-mass spectroscopy (LC/MS). Toxicokinetic studies indicated that TBBPA shows relatively a short half-life (7-9 h) and was eliminated almost completely in feces by 2 d. Based on the results from the 14-d repeated-dose study, TBBPA did not accumulate in the rat, and was eliminated in feces. The present results suggested that TBBPA may not be toxic to kidney, as the chemical is not bioavailable and is not present in renal tissue.