Genotoxicity and reproductive toxicity of bisphenol A and X-ray/bisphenol A combination in male mice

References

• Aikawa, H., Koyama, S., Matsuda, M., Nakahashi, K., Akazome, Y., Mori, T. (2004). Relief effect of vitamin A on the decreased motility of sperm and increased incidence of malformed sperm in mice exposed to bisphenol A. Cell Tissue Res 315:1119–1124.
   Google Scholar
• Al-Hiyasat, A. S., Darmani, H., Elbeticha, A. M. (2002). Effects of bisphenol A on adult male mouse fertility. Eu J Oral Sci 110:163–167.
   PubMed Web of Science ®Google Scholar
• Anderson, D., Basaran, N., Dobrzyńska, M. M., Basaran, A., Yu, T. W. (1997a). The modulating effects of flavonoid on food mutagens in human blood and sperm samples in the comet assay. Teratogen Carcinogen Mutagen 17:45–58.
   PubMedGoogle Scholar
• Anderson, D., Dobrzyńska, M. M., Yu, T. W. (1997b). Modulating effects of silymarin and myricetin on food mutagens and doxorubicin in assays with different genetic endpoints. J Environm Pathol Toxicol Oncol 16:313–327.
   Google Scholar
• Anderson, D., Yu, T. W., Phillip, B. J., Schmezer, P. (1994). The effects of various antioxidants and other modifying agents on oxygen-radical-generated damage in human lymphocytes in comet assay. Mutat Res 307:261–271.
   PubMed Web of Science ®Google Scholar
• Ashby, J., Tinwell, H., Lefevre, P. A., Joiner, R., Haseman, J. (2003). The effect on sperm production in adult Sprague-Dawley rats exposed by gavage to bisphenol A between postnatal days 91–97. Toxicol Sci 74:129–138.
   PubMed Web of Science ®Google Scholar
• Atkinson, A., Roy, D. (1995). Molecular dosimetry of DNA adducts in C3H mice treated with bisphenol A diglycidylether. Biochem Biophys Res Commun 210:424–433.
   PubMed Web of Science ®Google Scholar
• Aydogan, M., Korkmaz, A., Barlas, N., Kolankaya, D. (2010). Pro-oxidant effect of vitamin C coadministration with bisphenol A, nonylphenol, and octylphenol on the reproductive tract of male rats. Drug Chem Toxicol 33:193–203.
   PubMed Web of Science ®Google Scholar
• Bae, B., Jeong, J. H., Lee, S. J. (2002). The quantification and characterization of endocrine disruptor bisphenol A leaching from epoxy resin. Water Sci Technol 46:381–387.
   PubMed Web of Science ®Google Scholar
• Barrett, J. C. (1998). Bisphenol A induces cellular transformation, aneuploidy, and DNA adduct formation in cultured Syrian hamster embryo cells. Int J Cancer 75:290–294.
   PubMed Web of Science ®Google Scholar
• BEIR. (1990). Health effects of exposure to low levels of ionizing radiation. Committee on the Biological Effects on Ionizing Radiations. Board on Radiation Effects Research Commission on Life Sciences National Research Council. Washington DC: National Academy Press.
   Google Scholar
• Bennetts, L. E., Iuliis, G. N., Nixon, B., Kime, M., Zelski, K., McVicar, C. M., et al. (2008). Impact of estrogenic compounds on DNA integrity in human spermatozoa: evidence for cross-linking and redox cycling activities. Mutat Res 641:1–11.
   PubMed Web of Science ®Google Scholar
• Brotons, J. A., Olea-Serrano, M. F., Villalobos, M., Pedraza, V. B., Olea, N. (1995). Xenoestrogens released from laquer coatings in food cans. Environ Health Perspect 103:608–612.
   PubMed Web of Science ®Google Scholar
• Carrera, P., de Migueal, M., López, J, de la Torre, C., Navarrete, M. H. (1998). In vivo reponse of mouse liver to γ-irradiation assessed by the comet assay. Mutat Res 413:23–31.
   PubMedGoogle Scholar
• Cavalieri, E. L., Li, K. M., Balu, N., Saeed, M., Devanesan, P., Higginbotham, S., et al. (2002). Catehol ortho-quinones: the electrophilic compounds that form depurinating DNA adducts and could initiate cancer and other diseases. Carcinogenesis 23:1071–1077.
   PubMed Web of Science ®Google Scholar
• Chen, Y., Liu, X., Pisha, E., Constantinou, A. I., Hua, Y., Shen, L., et al. (2000). A metabolite of equine estrogens, 4-hydroxyequilenin, induced DNA damage and apoptosis in breast cancer cell lines. Chem Res Toxicol 13:342–350.
   PubMed Web of Science ®Google Scholar
• Chitra, K. C., Latchoumycandane, C., Mathur, P. P. (2003a). Induction of oxidative stress by bisphenol A in the epididymal sperm of rats. Toxicology 185:119–127.
   PubMed Web of Science ®Google Scholar
• Chitra, K. C., Rao, K. R., Mathur, P. P. (2003b). Effect of bisphenol A and vitamin C on epididymis of adult rats: a histopathological and biochemical study. Asian J Androl 5:203–208.
   PubMed Web of Science ®Google Scholar
• Choi, S. M., Yoo, S. D., Lee, B. M. (2004). Toxicological characteristics of the endocrine-disrupting chemicals: developmental toxicity, carcinogenicity, and mutagenicity. J Toxicol Environ Health Part B 7:1–24.
   PubMed Web of Science ®Google Scholar
• Collins, B. W., Howard, D. R., Allen, J. W. (1992). Kinetochore-staining of spermatid micronuclei: studies of mice treated with X-radiation or acrylamide. Mutat Res 281:287–294.
   PubMed Web of Science ®Google Scholar
• Davis, D. L., Bradlow, H. L., Wolff, M., Woodruff, T., Hoel, D. G., Anton-Culver, H. (1993). Medical hypothesis: xenoestrogens as preventable causes of breast cancer. Environ Health Perspect 101:372–377.
   PubMed Web of Science ®Google Scholar
• Dessi-Fulgheri, F., Porrini, S., Farabollini, F. (2002). Effects of prenatal exposure to bisphenol A on play behavior of female and male juvenile rats. Environ Health Perspect 110:403–407.
   PubMed Web of Science ®Google Scholar
• Dobrzyńska, M. M., Gajewski, A. K. (2000). Induction of micronuclei in bone marrow and sperm head abnormalities after combined exposure of mice to low doses of X-rays and acrylamide. Teratogen Carcinogen Mutagen 20:133–140.
   PubMedGoogle Scholar
• Dobrzyńska, M. M. (2005). The effects in mice of combined treatments to X-rays and antineoplastic drugs in the comet assay. Toxicology 207:331–338.
   PubMed Web of Science ®Google Scholar
• Dobrzyńska, M. M. (2007). Assessment of DNA damage in multiple organs from mice exposed to X-rays or acrylamide or a combination of both using the comet assay. In Vivo 21:657–662.
   PubMed Web of Science ®Google Scholar
• Dobrzyńska, M. M., Radzikowska, J. (2010). Frequency of micronuclei in reticulocytes of male mice exposed to bisphenol A and to a combination of X-rays and bisphenol A. Ann Natl Inst Hyg 61:129–133.
   PubMedGoogle Scholar
• Drozdz, K., Wysokinski, D., Krupa, R., Wozniak, K. (2011). Bisphenol A-glycidal methacylate induces a broad spectrum of DNA damage in human lymphocytes. Arch Toxicol 85:1453–1461.
   PubMed Web of Science ®Google Scholar
• Durner, J., Dębiak, M., Burkle, A., Hickel, R., Reichl, F.-X. (2011). Induction of DNA strand breaks by dental composite components compared to X-ray exposure in human gingival fibroblasts. Arch Toxicol 85:143–148.
   PubMed Web of Science ®Google Scholar
• EFSA. (2006). Opinion of the Scientific Panel on Food Activities, Flavourings; Processing Aids and Materials in Contact with Food on a request from the Commission related to 2,20 bis(4-hydroxyphenyl) propane (bisphenol A) Question number EFSA-Q-2005-100. EFSA J 428:1–75.
   Google Scholar
• Elliott, A. (2009). Issues in medical exposure. J Radiat Prot 29:A107–A121.
   Web of Science ®Google Scholar
• Haighton, L. A., Hlywka, J. J., Doull, J., Kroes, R., Lynch, B. S., Munro, I. C. (2002). An evaluation of the possible carcinogenicity of bisphenol A to humans. Regul Toxicol Pharmacol 35:199–205.
   Google Scholar
• Haines, G. A., Hendry, J. H., Daniel, C. P., Morris, I. D. (2001). Increased levels of comet-detected spermatozoa DNA damage following in vivo isotopic- or X-rays-irradiation of spermatogonia. Mutat Res 495:21–32.
   PubMed Web of Science ®Google Scholar
• Haines, G. A., Hendry, J. H., Daniel, C. P., Morris, I. D. (2002). Germ cell and dose-dependent DNA damage measured by comet assay in murine spermatozoa after testicular X-irradiation. Biol Reprod 67:854–861.
   PubMed Web of Science ®Google Scholar
• Harrison, A., Moore, P. C. (1980). Reduction in sperm count and increase in abnormal sperm in the mouse following X-radiation or injection of 22Na. Health Phys 39:219–224.
   PubMed Web of Science ®Google Scholar
• Hereth, C. B., Jin, W., Watanabe, G., Arai, K., Suzuki, A. K., Taya, K. (2004). Adverse effects of environmental toxicants, octylphenol and bisphenol A, on male reproductive function in pubertal rats. Endocrine 25:163–172.
   PubMed Web of Science ®Google Scholar
• Howe, S. R., Borodinsky, L. (1998). Potential exposure to bisphenol A from food-contact use of polycarbonate resins. Food Addit Contam 15:370–375.
   PubMedGoogle Scholar
• Hunt, P. A., Koehler, K. E., Susiarjo, M., Hodges, C. A., Ilagan, A., Volgt, R. C., et al. (2003). Bisphenol A exposure causes meiotic aneuploidy in the female mouse. Curr Biol 13:546–553.
   PubMed Web of Science ®Google Scholar
• Izzotti, A., Longobardi, M., Cartiglia, C., D’Agostini, F., Kanitz, S., De Flora, S. (2010). Pharmacological modulation of genome and proteome alterations in mice treated with the endocrine disruptor bisphenol A. Curr Cancer Drug Targets 10:147–154.
   PubMed Web of Science ®Google Scholar
• Końca, K., Lankoff, A., Banasik, A., Lisowska, H., Kuszewski, T., Góźdź, S., et al. (2003). A cross-platform public domain PC image-analysis program for comet assay. Mutat Res 534:15–20.
   PubMed Web of Science ®Google Scholar
• Lyons, G. (2000). Bisphenol A: a known endocrine disruptor. WWF European Toxics Programme Report. Surrey, UK: European Toxics Programme.
   Google Scholar
• Markey, C. M., Luque, E. H., Munoz De Toro, M., Sonnenschein, C., Soto, A. M. (2001). In utero exposure to bisphenol A alters the development and tissue organization of the mouse mammary gland. Biol Reprod 65:1215–1225.
   PubMed Web of Science ®Google Scholar
• Meeker, J. D., Shelley, E., Toth, T. L., Wright, D. L., Calafat, A. M., Trisini, A. T., et al. (2010). Semen quality and sperm DNA damage in relation to urinary bisphenol A among men from infertility clinic. Reprod Toxicol 30:532–539.
   PubMed Web of Science ®Google Scholar
• Mendiola-Cruz, M. T., Morales-Ramirez, P. (1999). Repair kinetics of gamma-ray induced DNA damage determined by single gel electrophoresis assay in murine leukocyte in vivo. Mutat Res 433:45–52.
   PubMed Web of Science ®Google Scholar
• Mobley, J. A., Brueggemeier, R. W. (2004). Estrogen receptor-mediated regulation of oxidative stress and DNA damage in breast cancer. Carcinogenesis 25:3–9.
   PubMed Web of Science ®Google Scholar
• Mutou, Y., Ibukl, Y., Terao, Y., Kojima, S., Goto, R. (2006). Change of estrogenic activity and release of chloride ion in chlorinated bisphenol A after exposure to ultraviolet B. Biol Pharm Bull 29:216–219.
   PubMedGoogle Scholar
• Naik, P., Vijayalaxmi, K. K. (2009). Cytogenetic evaluation for genotoxicity of bisphenol A in bone marrow cells of Swiss albino mice. Mutat Res 676:106–112.
   PubMed Web of Science ®Google Scholar
• Pacchierotti, F., Ranaldi, R., Eichenlaub-Ritter, U., Attia, S., Adler, I. D. (2008). Evaluation of aneugenic effects of bisphenol A in somatic and germ cells of the mouse. Mutat Res 651:64–70.
   PubMed Web of Science ®Google Scholar
• Park, D. H., Jang, H. Y., Park, C. K., Cheong, H. T., Kim, C. I., Yank, B. H. (2004). Effect of bisphenol A administration on reproductive characteristic and blood metabolite in mice. J Anim Sci Technol 46:957–966.
   Google Scholar
• Paz-Elizur, T., Sevilva, Z., Leitner-Dagan, Y., Elinger, D., Roisman, L. C., Livneh, Z. (2008). DNA repair of oxidative DNA damage in human carcinogenesis: potential application for cancer risk assessment and prevention. Cancer Lett 266:60–72.
   PubMed Web of Science ®Google Scholar
• Pollycove, M. (1998). Nonlinearity of radiation health effects. Environ Health Perspect 106:363–369.
   PubMed Web of Science ®Google Scholar
• Pollycove, M., Feinendegen, L. E. (2003). Radiation reduced versus endogenous DNA damage possible effect of inducible protective responses in mitigating endogenous damage. Hum Exp Toxicol 22:290–306.
   PubMed Web of Science ®Google Scholar
• Rosenfeld, E. J., Linden, K. G. (2004). Degradation of endocrine disrupting chemicals bisphenol A, ethinyl estradiol, and estradiol during UV photolysis and advanced oxidation processes. Environ Sci Technol 38:5476–5483.
   PubMed Web of Science ®Google Scholar
• Sakue, M, Ohsaho, S, Ishimura, R, Kurosawa, S, Kurohmaru, M, Hayashi, Y, et al. (2001). Bisphenol A affects spermatogenesis in the adult rat even at low dose. J Occupat Health 43:185–190.
   Web of Science ®Google Scholar
• Schonfelder, G., Friedrich, K., Paul, M., Chahoud, I. (2004). Developmental effects of prenatal exposure to bisphenol A on the uterus of rat offspring. Neoplasia 6:584–594.
   PubMed Web of Science ®Google Scholar
• Searle, A. G., Beechey, C. V. (1974). Sperm count, egg-fertilization, and dominant lethality after X-irradiation of mice. Mutat Res 22:69–74.
   Google Scholar
• Sharpe, R. M., Skakkebaek, N. E. (1993). Are oestrogens involved in failing sperm count and disorders of the male reproductive tract? Lancet 341:1392–1395.
   PubMed Web of Science ®Google Scholar
• Singh, N. P., McCoy, M., Tice, R. R., Schneider, E. L. (1988). A simple technique for quantization of low level of DNA damage in individual cells. Exp Cell Res 175:184–191.
   PubMed Web of Science ®Google Scholar
• Skakkebaek, N. E., Meyts, E. R., Jorgensen, N., Carlson, E., Petersen, P. M., Giwercman, A., et al. (1998). Germ cells cancer disorders of spermatogenesis: an environmental connection? APMIS 106:3–11.
   PubMed Web of Science ®Google Scholar
• Takao, Y., Lee, H. C., Kohra, S., Arizono, K. (2002). Release of bisphenol A from food can lining upon heating. J Health Sci 48:331–334.
   Web of Science ®Google Scholar
• Toyama, Y., Suzuki-Toyoata, F., Maekawa, M., Ito, C., Toshimori, K. (2004). Adverse effects of bisphenol A to spermatogenesis in mice and rats. Arch Histol Cytol 67:373–381.
   PubMed Web of Science ®Google Scholar
• Tyl, R. W., Myers, C. B., Marr, M. C., Thomas, B. F., Keimowitz, A. R., Brine, D. R., et al. (2002). Three-generation reproductive toxicity study of dietary bisphenol A in CD Sprague-Dawley rats. Toxicol Sci 68:121–146.
   PubMed Web of Science ®Google Scholar
• Ulutas, O. K., Yidiz, N., Durmaz, E., Ahab, M. A., Barlas, N., Cok, I. (2011). An in vivo assessment of the genotoxic potential of bisphenol A and 4-tert-octylphenol in rats. Arch Toxicol 85:995–1001.
   PubMed Web of Science ®Google Scholar
• U.S. EPA. (2008). Bisphenol A. Integrated risk inflamation system (IRIS). Available at: http//toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?IRIS.
   Google Scholar
• vom Saal, F. S., Cooke, P. S., Buchanan, D. L., Palanza, P., Thayer, K. A., Nagel, S. C., et al. (1998). A physiologically based approach to the study of bisphenol A and other estrogenic chemicals on the size of reproductive organs, daily sperm production, and behavior. Toxicol Ind Health 14:239–260.
   PubMed Web of Science ®Google Scholar
• Welshons, W. V., Thayer, K. A., Judy, B. M., Taylor, J. A., Curran, E. M., vom Saal, FS. (2003). Large effects from small exposure. I. Mechanisms for endocrine-disrupting chemicals with estrogenic activity. Environ Health Perspect 111:994–1006.
   Google Scholar
• Wetherill, Y. B., Petre, C. E., Monk, K. R., Puga, A., and Knudsen, K. E. (2002). The xenoestrogen bisphenol A induces inappropriate androgen receptor activation and mitogenesis in prostatic adenocarcinoma cells. Mol Cancer Ther 1:515–524.
   PubMed Web of Science ®Google Scholar
• Working, P. K., Bus, J. S., Hamm, T. E. Jr (1985). Reproductive effects of inhaled methyl chloride in the male Fisher 344 rat. II. Spermatogonial toxicity and sperm quality. Toxicol Appl Pharm 77:144–157.
   PubMed Web of Science ®Google Scholar
• Wyrobek, A. J., Bruce, W. R. (1975). Chemical induction of sperm abnormalities in mice. Proceed Nat Acad Sci U S A 72:4425–4429.
   PubMed Web of Science ®Google Scholar
• Yamamoto, T., Yasuhara, A. (1999). Quantities of bisphenol A leached from plastic waste samples. Chemosphere 38:2569–2576.
   PubMed Web of Science ®Google Scholar
• Yoshida, T., Horie, M., Hoshino, Y., and Nakazawa, H. (2001). Determination of bisphenol A in canned vegetables and fruit by high performance liquid chromatography. Food Addit Contam 15:370–375.
   Google Scholar