DOI QR코드

DOI QR Code

Toxicity Evaluation of Endocrine Disrupting Chemicals Using Human HepG2 Cell Line, Lumbricus rubellus and Saccharomyces cerevisiae

HepG2 인간 세포주, Lumbricus rubellus 및 Saccharomyces cerevisiae를 이용한 내분비교란물질의 독성평가

  • Sohn, Ho-Yong (Dept. of Food and Nutrition, Andong National University) ;
  • Kim, Hong-Ju (Dept. of Food and Nutrition, Andong National University) ;
  • Kum, Eun-Joo (Dept. of Food and Nutrition, Andong National University) ;
  • Cho, Min-Seop (The School of Bioresource Sciences, Andong National University) ;
  • Lee, Jung-Bok (The School of Bioresource Sciences, Andong National University) ;
  • Kim, Jong-Sik (Dept. of Biological Science, Andong National University) ;
  • Kwon, Gi-Seok (The School of Bioresource Sciences, Andong National University)
  • 손호용 (안동대학교 식품영양학과) ;
  • 김홍주 (안동대학교 식품영양학과) ;
  • 금은주 (안동대학교 식품영양학과) ;
  • 조민섭 (안동대학교 생명자원과학부) ;
  • 이중복 (안동대학교 생명자원과학부) ;
  • 김종식 (안동대학교 생명과학과) ;
  • 권기석 (안동대학교 생명자원과학부)
  • Published : 2006.10.01

Abstract

Toxicity evaluation systems for various chemicals and their metabolites have been developed during last decades. In this study, the acute toxicity of endocrine disrupting chemicals, such as endosulfan, bisphenol A, vinclozolin, and 3,5-dichloroaniline, was evaluated using HepG2 cell line, Lumbricus rubellus and Saccharomyces cerevisiae, respectively. The extents of toxicity of the chemicals in different bioassay systems varied substantially, such as endosulfan>3,5-dichloroaniline> bisphenol A in HepG2 cell line system, endosulfan>bisphenol A>3,5-dichloro aniline in L. rubellus system, and 3,5-dichloroaniline>endosulfan>bisphenol A in S. cerevisiae system. Meanwhile, no cytotoxicity was observed by treatment of vinclozolin in the evaluation systems. Our results suggest that earthworm and yeast are useful to evaluate acute toxicity of endocrine disrupting chemicals, and direct comparison of toxicity data from different bioassay systems is unattainable. Based on our results, we propose that the bioassay system with earthworm or yeast, a rapid, simple and economic system, could be applied as pre-test for the toxicity evaluation using human cell line or animals.

다양한 독성물질 및 이들의 대사산물의 효율적인 생물독성 평가시스템이 지속적으로 개발되고 있다. 본 연구에서는 대분비계 교란물질인 endosulfan, bisphenol A, vinclozolin 및 3,5-dichloroaniline을 대상으로 인간 간암세포주, 지렁이, 효모를 이용한 세포독성 및 성장억제 효과를 평가하였다. 인간 간암세포주 독성평가에서는 endosulfan, 3,5-dichloroaniline, bisphenol A의 순으로 독성이 나타났으며, 지렁이 독성평가에서는 endosulfan, bisphenol A, 3,5-dichloroaniline의 순으로 독성이 나타났다. 효모를 이용한 독성평가에서는 3,5-dichloroaniline, endosulfan, bisphenol A의 순으로 독성이 나타나 다른 시스템과는 부분적인 차이가 나타났으며, vinclozolin의 경우 3가지 독성평가 시스템에서 모두 독성이 나타나지 않았다. 이러한 결과는, 동일한 물질을 서로 다른 생물 독성평가 시스템을 사용하여 평가하는 경우, 부분적인 오류가 나타날 수 있음을 암시하고 있으며, 독성 유무 판단은 가능하더라도, 독성 정량평가 및 독성 정도를 비교하는 것은 어렵다는 것을 제시하고 있다. 또한 본 결과는, 다양한 물질 및 이들의 대사산물의 일차적 독성평가에는 지렁이 및 효모시스템이 빠르고 경제적임을 암시하고 있으며, 독성이 인정될 경우 인간세포주 및 동물시험에 의한 검증이 효율적이라고 판단된다.

Keywords

References

  1. Ahn, K.-S., K.-Y. Lee, H.-J. Kang, S.-K. Park, and G.-H. Kim. 2004. Toxicity of pestcides to minute pirate bug, Orius strigicollis Poppius (Hemiptera: Anthocoridae), a predator of thrips. Kor. J. Appl. Entomol. 43, 257-262
  2. An, Y. J. 2005. Assessing soil ecotoxicity of methyl tert-butyl ether using earthworm bioassay; closed soil microcosm test for volatile organic compounds. Environ. Pollut. 134, 181-186 https://doi.org/10.1016/j.envpol.2004.08.012
  3. Awasthi, N., A. K. Singh, R. K. Jain, B. S. Khangarot and A. Kumar. 2003. Degradation and detoxification of endosulfan isomers by a defined co-culture of two Bacillus strains. Appl. Microbiol. Biotechnol. 62, 279-283 https://doi.org/10.1007/s00253-003-1241-7
  4. Bayoumi, A. E., A. J. Garcia-Fernandez, C. Ordonez, Y. Perez-Pertejo, J. C. Cubria, R. M. Reguera, R. Balana- Fouce, and D. Ordonez. 2001. Cyclodiene organochlorine insecticide-indued alternations in the sulfur-redox cycle in CHO-K1 cells. Comp. Biochem. Physiol. Part C. 130, 315-323
  5. Bonefeld-Jorgensen, E. C., H. T. Grunfeld, and I. M. Giermandsen. 2005. Effect of pesticides on estrogen receptor transactivation in vitro: A comparison of stable transfected MVLN and transient transfected MCF-7 cells. Mol. Cell Endocrinol. 244, 20-30 https://doi.org/10.1016/j.mce.2005.01.017
  6. Charrois, J. W., W. B. McGill and K. L. Froese. 2001. Acute ecotoxicity of creosote-contaminated soils to Eisenia fetida: a survival-based approach. Environ. Toxicol. Chem.. 20, 2594-2603 https://doi.org/10.1002/etc.5620201127
  7. Conder J. M. and R. P. Lanno. 2000. Evaluation of surrogate measures of cadmium, lead, and zinc bioavailability to Eisenia fetida. Chemosphere 41, 1659-1668 https://doi.org/10.1016/S0045-6535(00)00045-X
  8. Graumann, K., A. Breithofer, and A, Jungbauer. 1999. Monitoring of estrogen mimics by a recombinant yeast assay: synergy between natural and synthetic compounds?. Sci. Total Environ. 225, 69-79 https://doi.org/10.1016/S0048-9697(99)80018-7
  9. Greenman S.B., M. J. Rutten, W. M. Fowler, L. Scheffler, L, A, Shortridge, B. Brown, B. C. Sheppard, K. E. Deveney, C. W. Deveney, D. D. Trunkey. 1997. Herbicide/pesticide effects on intestinal epithelial growth. Environ. Res. 75, 85-93 https://doi.org/10.1006/enrs.1997.3766
  10. Jung, H., W. Park, J. Lee, J. W. Yoo, E. Y. Kim and H. J. Chae. 2005. Toxicity test of biodiesel and biodiesel-derived neopentyl polyol ester lubricant oil base using earthworm. Korean J. Biotechnol. Bioeng. 20, 84-87
  11. Kang, J.-H., Y. Katayama, and F. Kondo. 2006. Biodegradation or metabolism of bisphenol A: From microorganisms to mammals. Toxicol. 217, 81-90 https://doi.org/10.1016/j.tox.2005.10.001
  12. Kannan, K., R. F. Holcombe, S. K. Jain, X. Alvarez- Hermandez, R. Chervenak, R. E. Wolf, and J. Glass. 2000. Evidence for the induction of apoptosis by endosulfan in a human T-cell leukemic line. Mol. Cell Biochem. 205, 53-66 https://doi.org/10.1023/A:1007080910396
  13. Kaur, I., R. P. Mathur, S. N. Tandon and P. Dureja. 1998. Persistence of endosulfan (technical) in water and soil. Environ. Tech. 19, 115-119 https://doi.org/10.1080/09593331908616663
  14. Kullman, S. W. and F. Matsumura. 1996. Metabolic pathways utilized by Phanerochaete chrysosporium for degradation of the cyclodiene pesticide endosulfan. Appl. Environ. Microbiol. 62, 593-600
  15. Kwon, G.-S., H.-Y. Sohn, K-.S. Shin, E. Kim and B.-I. Seo. 2005. Biodegradation of the organochlorine insecticide, endosulfan, an the toxic metabolite, endosulfan sulfate, by Klebsiella oxytoca KE-8. Appl. Microbiol. Biotechnol. 67, 845-850 https://doi.org/10.1007/s00253-004-1879-9
  16. Kwon, G.-S., J.-E. Kim, T.-E. Kim, H.-Y. Sohn, S.-C. Koh, K.-S. Shin and D.-G. Kim. 2002. Klebsiella pneumoniae KE-1 degrades endosulfan without formation of the toxic metabolite, endosulfan sulfate. FEMS Miobiol. Lett. 215, 255-259 https://doi.org/10.1111/j.1574-6968.2002.tb11399.x
  17. Lee, S.-E., J.-S. Kim, I.-R. Kennedy, J.-W. Park, G.-S. Kwon, S.-C. Koh and J.-E. Kim. 2003. Biotransformation of an organochlorine insecticide, endosulfan, by Anabaena species. J. Agric. Food Chem. 51, 1336-1340 https://doi.org/10.1021/jf0257289
  18. Lee, Y.-D., I.-B. Ko, and W.-S. Shin. 2005. Toxicity assessment of biocide using Chlamydomonas reinhardtii. J. Kor. Soc. Water Quality 21, 332-336
  19. Maul, J. D., J. B. Belden, B. A. Schwab, M. R. Whiles, B. Spears, J. L. Farris, and M. J. Lydy. 2006. Bioaccumulation and trophic transfer of polychlorinated biphenyls by aquatic and terrestrial insects to tree swallows (Tachycineta bicolor). Environ. Toxicol. Chem. 25, 1017-1025 https://doi.org/10.1897/05-309R.1
  20. Mutou, Y., Y. Ibuki, T, Y. Terao, S. Kojima, and R. Goto. 2006. Chemical changes of chlorinated bisphenol A by ultraviolet irriadition and cytotoxicity of their products on Jurkat cells. Environ. Toxicol. Pharmcol. 21, 283-289 https://doi.org/10.1016/j.etap.2005.09.005
  21. Na, Y. E., H. S. Bang, K. K. Kang, M. S. Han and Y. J. Ahn. 2005. Assessment of the effects of some insecticides on mortality of earthworm (Eisenia fetida). Korean J. Environ. Agr. 24, 289-294 https://doi.org/10.5338/KJEA.2005.24.3.289
  22. Ooe, H., T, Taira, S. M. Iguchi-Ariga, H. Ariga. 2005. Induction of reactive oxygen species by bisphenol A and abrogation of bisphenol A-induced cell injury by DJ-1. Toxicol. Sci. 88, 114-126 https://doi.org/10.1093/toxsci/kfi278
  23. Patin S. A. 1982. Pollution and biological resources of the oceans, butter worth. Scientific press, London, pp 80-109
  24. Sekine, Y., T. Yamamoto, T. Yumioka, S. Imoto, H. Kojima, and T. Matsuda. 2004. Cross-talk between endocrine- disrupting chemicals and cytokine signaling through estrogen receptors. Biochem. Biophys. Res. Comm. 315, 692-698 https://doi.org/10.1016/j.bbrc.2004.01.109
  25. Sohn, H.-Y., H.-J. Kim, E.-J. Kum, J.-B. Lee, and G.-S. Kwon. 2006. Simple and rapid evaluation system for endosulfan toxicity and selection of endosulfan detoxifying microorganism based on Lumbricus rubellus. Kor. J. Life Sci. 16, 108-113 https://doi.org/10.5352/JLS.2006.16.1.108
  26. Sohn, H.-Y., C.-S. Kwon, G.-S. Kwon, J.-B. Lee and E. Kim. 2004. Induction of oxidative stress by endosulfan and protective effect of lipid-soluble antioxidants against endosulfan-induced oxidative damage. Toxicol. Lett. 151, 357-365 https://doi.org/10.1016/j.toxlet.2004.03.004
  27. Sohn, H.-Y., E.-J. Kum, C.-S. Kwon, J.-S. Kim, and G.-S. Kwon. 2006. Involvement of oxidative stress in cytotoxicity of bisphenol A of Saccharomyces cerevisiae. FEMS Microbiol Lett. Submitted
  28. Sutherland, T. D., I. Horne, R. L. Harcourt, R. J. Russell and J. G. Oakeshott. 2002. Isolation and characterization of a Mycobacterium strain that metabolizes the insecticide endosulfan. J. Appl. Microbiol. 93, 380-389 https://doi.org/10.1046/j.1365-2672.2002.01728.x
  29. Staples, C. A., P. B. Dorn, G. M. Klecka, S. T. O'Block, and L. R. Harris. 1998. A review of the environmental fate, effects, and exposures of bisphenol A. Chemosphere 36, 2149-2173 https://doi.org/10.1016/S0045-6535(97)10133-3
  30. Vanni, A., R. Gamberini, A. Calabria, and V. Pellegrino. 2000. Determination of presence of fungicides by their common metabolites, 3,5-DCA, in compost. Chemosphere 41, 453-458 https://doi.org/10.1016/S0045-6535(99)00223-4
  31. Wu, X. J., W. Q. Lu, P. H. Roos, and V. Mersch- Sundermann. 2005. Vinclozolin, a widely used fungizide, enhanced BaP-induced micronucleus formation in human derived hepatoma cells by increasing CYP1A1 expression. Toxicol Lett. 159, 83-88 https://doi.org/10.1016/j.toxlet.2005.04.010
  32. Zhan, M., X. Yang, Q. Xian, and L. Kong. 2006. Photosensitized degradation of bisphenol A involving reactive oxygen species in the presence of humic substances. Chemosphere 63, 378-386 https://doi.org/10.1016/j.chemosphere.2005.08.046

Cited by

  1. Spectrophotometric Determination of Bisphenol A by Complexation with Ferricyanide and Ferric chloride solution vol.17, pp.2, 2007, https://doi.org/10.5352/JLS.2007.17.2.266