Transmembrane transports of acrylamide and bisphenol A and effects on development of zebrafish (Danio rerio)

Journal of Hazardous Materials

Volumn 184, Issue 1-3, 2010, Pages 81-88

  Fei, Xun Chang ^a,b   Song, Chao ^a   Gao, Hong Wen ^a  

^a TONGJI UNIVERSITY   (China)

^b UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Acrylamide; Bisphenol A; Development; Transmembrane transport; Zebrafish (Danio rerio)

Indexed keywords

ACRYLAMIDES; BISPHENOL A; DEVELOPMENT; TRANSMEMBRANE TRANSPORT; ZEBRAFISH;

AMIDES; CELLS; CYTOLOGY; HYDROGEN BONDS; PHENOLS; VAN DER WAALS FORCES;

TOXICITY;

4,4' ISOPROPYLIDENEDIPHENOL; ACRYLAMIDE;

BIOACCUMULATION; CHEMICAL BONDING; CHEMICAL POLLUTANT; CYPRINID; CYTOPLASM; INHIBITION; MALNUTRITION; MEMBRANE; PHENOL; POLLUTION EFFECT; TOXICITY;

ARTICLE; CYTOPLASM; EMBRYO; EMBRYO DEVELOPMENT; EMBRYOTOXICITY; HYDROGEN BOND; IONIC STRENGTH; MALNUTRITION; MEMBRANE TRANSPORT; NONHUMAN; OUTER MEMBRANE; PH; TEMPERATURE SENSITIVITY; ZEBRA FISH;

ACRYLAMIDE; ANIMALS; BIOLOGICAL TRANSPORT; CELL MEMBRANE; HYDROGEN-ION CONCENTRATION; MICROSCOPY, ELECTRON, SCANNING; OSMOLAR CONCENTRATION; PHENOLS; SPECTROMETRY, FLUORESCENCE; TEMPERATURE; ZEBRAFISH;

DANIO RERIO;

EID: 77957868098     PISSN: 03043894     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2010.08.007     Document Type: Article

References (54)

1. Wu L.L., Gao H.W., Gao N.Y., Chen F.F., Chen L. Interaction of perfluorooctanoic acid with human serum albumin. BMC Struct. Biol. 2009, 9:31.
2. Gao H.W., Xu Q., Chen L., Wang S.L., Wang Y., Wu L.L., Yuan Y. Potential protein toxicity of synthetic pigments: Binding of poncean S to human serum albumin. Biophys. J. 2008, 94:906-917.
3. Chen F.F., Tang Y.N., Wang S.L., Gao H.W. Binding of brilliant red compound to lysozyme: Insights into the enzyme toxicity of water-soluble aromatic chemicals. Amino Acids 2009, 36:399-407.
4. Wu L.L., Chen L., Song C., Liu X.W., Deng H.P., Gao N.Y., Gao H.W. Potential enzyme toxicity of PFOA. Amino Acids 2010, 38:113-116.
5. 2 with lysozyme: Insights into the enzyme toxicity of nanosized particles. Environ. Sci. Pollut. Res. 2010, 17:798-806.
6. Salian S., Doshi T., Vanage G. Impairment in protein expression profile of testicular steroid receptor coregulators in male rat offspring perinatally exposed to bisphenol A. Life Sci. 2009, 85:11-18.
7. Nakayama K., Iwata H., Kim E.Y., Tashiro K., Tanabe S. Gene expression profiling in common cormorant liver with an oligo array: assessing the potential toxic effects of environmental contaminants. Environ. Sci. Technol. 2006, 40:1076-1083.
8. Ramakrishnan S., Wayne N.L. Impact of bisphenol-A on early embryonic development and reproductive maturation. Reprod. Toxicol. 2008, 25:177-183.
9. Li L., Gao H.W., Ren J.R., Chen L., Li Y.C., Zhao J.F., Zhao H.P., Yuan Y. Binding of Sudan II and IV to lecithin liposomes and E-coli membranes: insights into the toxicity of hydrophobic azo dyes. BMC Struct. Biol. 2007, 7:16.
10. IARC, International Agency for Research on Cancer (IARC) monographs on the evaluation of the carcinogenic risk of chemicals to humans: some industrial chemicals, Lyon (France), Int. Agency Res. Cancer (IARC) 60 (1994) 389-443.
11. LoPachin R.M. The changing view of acrylamide neurotoxicity. Neurotoxicology 2004, 25:617-630.
12. Costa L.G. Biomarker research in neurotoxicology: the role of mechanistic studies to bridge the gap between the laboratory and epidemiological investigations. Environ. Health Persp. 1996, 104:55-67.
13. Besaratinia A., Pfeifer G.P. Genotoxicity of acrylamide and glycidamide. J. Natl. Cancer Inst. 2004, 96:1023-1029.
14. Besaratinia A., Pfeifer G.P. Weak yet distinct mutagenicity of acrylamide in mammalian cells. J. Natl. Cancer Inst. 2003, 95:889-896.
15. Martins C., Oliveira N.G., Pingarilho M., da Costa G.G., Martins V., Marques M.M., Beland F.A., Churchwell M.I., Doerge D.R., Rueff J., Gaspar J.F. Cytogenetic damage induced by acrylamide and glycidamide in mammalian cells: correlation with specific glycidamide-DNA adducts. Toxicol. Sci. 2007, 95:383-390.
16. Tyl R.W., Friedman M.A. Effects of acrylamide on rodent reproductive performance. Reprod. Toxicol. 2003, 17:1-13.
17. WHO FAO/WHO Consultation on the Health Implications of Acrylamide in Food-Summary Report 2002, WHO, Geneva (Switzerland), pp. 1-12.
18. Mottram D.S., Wedzicha B.L., Dodson A.T. Acrylamide is formed in the Maillard reaction. Nature 2002, 419:448-449.
19. Stadler R.H., Blank I., Varga N., Robert F., Hau J., Guy P.A., Robert M.C., Riediker S. Acrylamide from Maillard reaction products. Nature 2002, 419:449-450.
20. Staples C.A., Woodburn K., Caspers N., Hall A.T., Klecka G.M. A weight of evidence approach to the aquatic hazard assessment of bisphenol A. Hum. Ecol. Risk Assess. 2002, 8:1083-1105.
21. Staples C.A., Dorn P.B., Klecka G.M., O'Block S.T., Harris L.R. A review of the environmental fate, effects, and exposures of bisphenol A. Chemosphere 1998, 36:2149-2173.
22. EU, The opinion of the European food safety authority on the re-assessment of bisphenol A, 2007. http://ecb.jrc.it/documents/Existing-Chemicals/RISK_ASSESSMENT/ADDENDUM/bisphenola_add_325.pdf.
23. Goodson A., Summerfield W., Cooper I. Survey of bisphenol A and bisphenol F in canned foods. Food Addit. Contam. 2002, 19:796-802.
24. Behnisch P.A., Hosoe K., Sakai S. Combinatorial bio/chemical analysis of dioxin and dioxin-like compounds in waste recycling, feed/food, humans/wildlife and the environment. Environ. Int. 2001, 27:495-519.
25. Yamamoto T., Yasuhara A., Shiraishi H., Nakasugi O. Bisphenol A in hazardous waste landfill leachates. Chemosphere 2001, 42:415-418.
26. Olea N., OleaSerrano M.F. Oestrogens and the environment. Eur. J. Cancer Prev. 1996, 5:491-496.
27. Le H.H., Carlson E.M., Chua J.P., Belcher S.M., Bisphenol A is released from polycarbonate drinking bottles and mimics the neurotoxic actions of estrogen in developing cerebellar neurons. Toxicol. Lett. 2008, 176:149-156.
28. Sawai C., Anderson K., Walser-Kuntz D. Effect of bisphenol A on murine immune function: Modulation of interferon-gamma, IgG2a, and disease symptoms in NZB x NZW F-1 mice. Environ. Health Persp. 2003, 111:1883-1887.
29. Kim J.C., Shin H.C., Cha S.W., Koh W.S., Chung M.K., Han S.S. Evaluation of developmental toxicity in rats exposed to the environmental estrogen bisphenol A during pregnancy. Life Sci. 2001, 69:2611-2625.
30. Sohoni P., Tyler C.R., Hurd K., Caunter J., Hetheridge M., Williams T., Woods C., Evans M., Toy R., Gargas M., Sumpter J.P. Reproductive effects of long-term exposure to bisphenol A in the fathead minnow (Pimephales promelas). Environ. Sci. Technol. 2001, 35:2917-2925.
31. Niwa T., Fujimoto M., Kishimoto K., Yabusaki Y., Ishibashi F., Katagiri M. Metabolism and interaction of bisphenol A in human hepatic cytochrome p450 and steroidogenic CYP17. Biol. Pharm. Bull. 2001, 24:1064-1067.
32. Hiroi T., Okada K., Imaoka S., Osada M., Funae Y. Bisphenol A binds to protein disulfide isomerase and inhibits its enzymatic and hormone-binding activities. Endocrinology 2006, 147:2773-2780.
33. Yan H.M., Takamoto M., Sugane K. Exposure to bisphenol a prenatally or in adulthood promotes T(H)2 cytokine production associated with reduction of CD4(+)CD25(+) regulatory T cells. Environ. Health Persp. 2008, 116:514-519.
34. Dolinoy D.C., Huang D., Jirtle R.L. Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:13056-13061.
35. Dairkee S.H., Seok J., Champion S., Sayeed A., Mindrinos M., Xiao W.Z., Davis R.W., Goodson W.H. Bisphenol A induces a profile of tumor aggressiveness in high-risk cells from breast cancer patients. Cancer Res. 2008, 68:2076-2080.
36. Atkinson A., Roy D. In-vitro conversion of environmental estrogenic chemical bisphenol-A to DNA-binding metabolite(s). Biochem. Biophys. Res. Co. 1995, 210:424-433.
37. Kaddar N., Harthe C., Dechaud H., Mappus E., Pugeat M. Cutaneous penetration of bisphenol A in pig skin. J. Toxicol. Environ. Health A 2008, 71:471-473.
38. Nishizawa H., Morita M., Sugimoto M., Imanishi S., Manabe N. Effects of in utero exposure to bisphenol a on mRNA expression of arylhydrocarbon and retinoid receptors in murine embryos. J. Reprod. Dev. 2005, 51:315-324.
39. Hallare A.V., Kohler H.R., Triebskorn R. Development toxicity and stress protein responses in zebrafish embryos after exposure to diclofenac and its solvents, DMSO. Chemosphere 2004, 56:659-666.
40. Reimers M.J., Flockton A.R., Tanguay R.L. Ethanol- and acetaldehyde-mediated developmental toxicity in zebrafish. Neurotoxicol. Teratol. 2004, 26:769-781.
41. Nagel R. DarT: the embryo test with the zebrafish Danio rerio-a general model in ecotoxicology and toxicology. Altex-Altern. Tierexp. 2002, 19:38-48.
42. Lahnsteiner F. The sensitivity and reproducibility of the zebrafish (Danio rerio) embryo test for the screening of waste water quality and for testing the toxicity of chemicals. Atla-Altern. Lab. Anim. 2008, 36:299-311.
43. Lammer E., Carr G.J., Wendler K., Rawlings J.M., Belanger S.E., Braunbeck T. Is the fish embryo toxicity test (FET) with the zebrafish (Danio rerio) a potential alternative for the fish acute toxicity test?. Comp. Biochem. Phys. C 2009, 149:196-209.
44. Marguerie A., Buckley C., Fleming A. Validation of an embryo toxicology screen using zebrafish. Toxicol. Lett. 2006, 164:S220.
45. Song C., Gao N.Y., Gao H.W. Tranmembrane distribution of kanamycin and chloromycetin: insights into the cytotoxicity of antibacterial drugs. Mol. BioSyst. 2010, 6. 10.1039/b921810f.
46. Saar K., Lindgren M., Hansen M., Eiriksdottir E., Jiang Y., Rosenthal-Aizman K., Sassian M., Langel U. Cell-penetrating peptides: a comparative membrane toxicity study. Anal. Biochem. 2005, 345:55-65.
47. Gokmen V., Senyuva H.Z., Acar J., Sarioglu K. Determination of acrylamide in potato chips and crisps by high-performance liquid chromatography. J. Chromatogr. A 2005, 1088:193-199.
48. George O., Bryant B.K., Chinnasamy R., Corona C., Arterburn J.B., Shuster C.B. Bisphenol A directly targets tubulin to disrupt spindle organization in embryonic and somatic cells. ACS Chem. Biol. 2008, 3:167-179.
49. Kwon J.H., Liljestran H.M., Katz L.E., Yamamoto H. Partitioning thermodynamics of selected endocrine disruptors between water and synthetic membrane vesicles: effects of membrane compositions. Environ. Sci. Technol. 2007, 41:4011-4018.
50. Iso T., Watanabe T., Iwamoto T., Shimamoto A., Furuichi Y. DNA damage caused by bisphenol A and estradiol through estrogenic activity. Biol. Pharm. Bull. 2006, 29:206-210.
51. Pastva S.D., Villalobos S.A., Kannan K., Giesy J.P. Morphological effects of bisphenol-A on the early life stages of medaka (Oryzias latipes). Chemosphere 2001, 45:535-541.
52. Honkanen J.O., Holopainen I.J., Kukkonen J.V.K. Bisphenol A induces yolk-sac oedema and other adverse effects in landlocked salmon (Salmo salar m. sebago) yolk-sac fry. Chemosphere 2004, 55:187-196.
53. Tsutsui T., Tamura Y., Yagi E., Hasegawa K., Takahashi M., Maizumi N., Yamaguchi F., Barrett J.C. Bisphenol-A induces cellular transformation, aneuploidy and DNA adduct formation in cultured Syrian hamster embryo cells. Int. J. Cancer 1998, 75:290-294.
54. Chitra K.C., Latchoumycandane C., Mathur P.P. Induction of oxidative stress by bisphenol A in the epididymal sperm of rats. Toxicology 2003, 185:119-127.