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Study of the Toxicity of 1-Bromo-3-Chloro-5,5-Dimethylhydantoin to Zebrafish 被引量:3

Study of the Toxicity of 1-Bromo-3-Chloro-5,5-Dimethylhydantoin to Zebrafish
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摘要 Objective 1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH) is a solid oxidizing biocide for water disinfection.The objective of this study was to investigate the toxic effect of BCDMH on zebrafish.Methods The developmental toxicity of BCDMH on zebrafish embryos and the dose-effect relationship was determined.The effect of BCDMH exposure on histopathology and tissue antioxidant activity of adult zebrafish were observed over time.Results Exposure to 4 mg/L BCDMH post-fertilization was sufficient to induce a number of developmental malformations,such as edema,axial malformations,and reductions in heart rate and hatching rate.The no observable effects concentration of BCDMH on zebrafish embryo was 0.5 mg/L.After 96 h exposure,the 50% lethal concentration (95% confidence interval (CI)) of BCDMH on zebrafish embryo was 8.10 mg/L (6.15-11.16 mg/L).The 50% inhibitory concentration (95% CI) of BCDMH on hatching rate was 7.37 mg/L (6.33-8.35 mg/L).Histopathology showed two types of responses induced by BCDMH,defensive and compensatory.The extreme responses were marked hyperplasia of the gill epithelium with lamellar fusion and epidermal peeling.The histopathologic changes in the gills after 10 days exposure were accompanied by significantly higher catalase activity and lipid peroxidation.Conclusion These results have important implications for studies on the toxicity and use of BCDMH and its analogs. Objective 1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH) is a solid oxidizing biocide for water disinfection.The objective of this study was to investigate the toxic effect of BCDMH on zebrafish.Methods The developmental toxicity of BCDMH on zebrafish embryos and the dose-effect relationship was determined.The effect of BCDMH exposure on histopathology and tissue antioxidant activity of adult zebrafish were observed over time.Results Exposure to 4 mg/L BCDMH post-fertilization was sufficient to induce a number of developmental malformations,such as edema,axial malformations,and reductions in heart rate and hatching rate.The no observable effects concentration of BCDMH on zebrafish embryo was 0.5 mg/L.After 96 h exposure,the 50% lethal concentration (95% confidence interval (CI)) of BCDMH on zebrafish embryo was 8.10 mg/L (6.15-11.16 mg/L).The 50% inhibitory concentration (95% CI) of BCDMH on hatching rate was 7.37 mg/L (6.33-8.35 mg/L).Histopathology showed two types of responses induced by BCDMH,defensive and compensatory.The extreme responses were marked hyperplasia of the gill epithelium with lamellar fusion and epidermal peeling.The histopathologic changes in the gills after 10 days exposure were accompanied by significantly higher catalase activity and lipid peroxidation.Conclusion These results have important implications for studies on the toxicity and use of BCDMH and its analogs.
出处 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2011年第4期383-390,共8页 生物医学与环境科学(英文版)
基金 supported by the National Science and Technology Major Project "Creation of Major New Drugs", 2008ZX09305-001
关键词 Developmental toxicity Histopathological effects 1-Bromo-3-chloro-5 5-dimethylhydantoin (BCDMH) Developmental toxicity Histopathological effects 1-Bromo-3-chloro-5 5-dimethylhydantoin (BCDMH)
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  • 1Beihoffer J, Bour E, Lowry J, et al. Identification and determination of the isomeric bromo-and/or chloro-substituted 1, 3-dihalo-5, 5-dimethylhydantoins used in disinfectants and molluscicides. J AOAC Int, 1996; 79(4), 823-8.
  • 2Brycki B, Seifert K, Szymanska K, et al. The effect of oxidizing biocides on desulfurication and denitrification processes. Pot J Environ Stud, 2000; 9(5), 363-7.
  • 3Donohoe H, Mattner S, Brett R, et al. Status of methyl bromide phase-out in the temperate australian strawberry industry. In: Proc. Annu. Intl. Res. Conf. on MB Alts. and Emiss. Red. 5-9 November, San Diego, USA. 2001; pp 42-4.
  • 4Loushney E, Harrison J. Irritant contact dermatitis due to I-bromo-3-chloro-5, 5-dimethylhydantoin in a hydrotherapy pool. Risk assessments, the need for continuous evidence-based assessments. Occupational Medicine, 2998, 48{7). 461-3.
  • 5Berghmans S, Hunt J, Roach A, et al. Zebrafish offer the potential for a primary screen to identify a wide variety of potential anticonvulsants. Epilepsy Res, 2007; 75(1), 18-28.
  • 6Chiu L, Cunningham L, Raible D, et al. Using the zebrafish lateral line to screen for ototoxicity. J Assoc Res Otolaryngol, 2008; 9(2) 178-90.
  • 7Hill A, Teraoka H, Heideman W, et al. Zebrafish as a model vertebrate for investigating chemical toxicity. Toxicol Sci, 2005; 86(1), 6-19.
  • 8Richards F, Alderton W, Kimber G, et al. Validation of the use of zebrafish larvae in visual safety assessment. J Pharmacol Toxicol, 2008; 58(1), 50-8.
  • 9Spitsbergen J, Kent M. The state of the art of the zebrafish model for toxicology and toxicologic pathology research-advantages and current limitations. Toxicol Pathol, 2003; 31(1), 62-87.
  • 10Tran T, Sneed B, Haider J, et al. Automated, quantitative screening assay for antiangiogenic compounds using transgenic zebrafish. Cancer Res, 2007; 67(2), 12386-92.

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