Studies on the Reproductive Toxicant and Blood Metabolite in Pups Born After Bisphenol A Administration in Pregnant Mice

임신중인 생쥐에 Bisphenol A 투여 후 태어난 차산자의 생식독성과 혈액성분에 관한 연구

  • Park Dong-Heon (College of Animal Resource Science, Kangwon National University) ;
  • Jang Hyun-Yong (College of Animal Resource Science, Kangwon National University) ;
  • Kim Choung-Ik (College of Animal Resource Science, Kangwon National University) ;
  • Cheong Hee-Tae (College of Animal Resource Science, Kangwon National University) ;
  • Park Choon-Keun (College of Animal Resource Science, Kangwon National University) ;
  • Yang Boo-Keun (College of Animal Resource Science, Kangwon National University)
  • 박동헌 (강원대학교 동물자원과학대학) ;
  • 장현용 (강원대학교 동물자원과학대학) ;
  • 김정익 (강원대학교 동물자원과학대학) ;
  • 정희태 (강원대학교 동물자원과학대학) ;
  • 박춘근 (강원대학교 동물자원과학대학) ;
  • 양부근 (강원대학교 동물자원과학대학)
  • Published : 2005.06.01

Abstract

Bisphenol A (BPA) is a monomer used in the manufacture of a multitude of chemical products, including epoxy resins and polycarbonate. The objective of this study was to evaluate the effects of BPA administration on reproductive characteristics and blood hematological and chemical values in offspring of pregnant dams treated with BPA. BPA was administrated to pregnant mice by intraperitoneally injection with 0, 0.05, 0.5 and 5.0 mg/kg B.W. for 5 times at 3 days interval on gestation days 1-16. There were no treatment-related effects of BPA on reproductive organ weight in male offsprings at 45 days-of-age, but body weight was the lowest in 5.0mg BPA group when compared to other groups (P<0.05). No differences in semen characteristics (sperm concentration, viability, motility and abnormality) were observed between the control and BPA treatment groups. The WBC, HB, HT, MCV, MCH, MCHC, albumin, BUN and total protein of blood hematological and chemical values in male offsprings were not difference for any treatment groups, but RBC value in BPA groups was significantly increased comparing to the control group (P<0.05). The PLT value was slightly higher in 5.0mg BPA groups than in any other group, but not significantly difference among the experimental groups. In female offsprings, the effects of BPA didn't affect to the body and ovary weight, but the uterus weight in 5.0mg BPA group was slightly heavier than that of control group (P>0.05). No statically significant difference in blood hematological values in female offsprings were observed between the control group and BPA groups, but the concentration of albumin and BUN were significantly higher in 0.5mg BPA group when compared to control and other BPA treatment groups (P<0.05). The histological evaluation of testis and ovary in growing offspring at 45 days-of-age was not difference between the control group and BPA groups, but endometriosis of the uterus in female offspring was dramatically increased in 0.5 and 5.0mg BPA groups. These founding suggest that low concentration of BPA might not have a important role on reproductive ability or blood metabolite in offspring of pregnant dams treated with BPA.

Keywords

References

  1. Ashby, B., Tinwell, H. and Haseman, J. (1999): Lack of effects for low dose levels of bisphenol A and diethylstilbestrol on the prostate gland of CF1 mice exposed in utero. Regula. Toxicol. Pharma., 30, 156-166 https://doi.org/10.1006/rtph.1999.1317
  2. Atinson, A. and Roy, D. (1995): In vitro DNA adduct formation by bisphenol A. Environ. Mol. Mutagen., 26, 60-66 https://doi.org/10.1002/em.2850260109
  3. Brotons, J.A., Olea-serrano, M.F., Villalobos, M., Pedraza, V. and Olea, N. (1995): Xenoestrogens released from lacquer coatings in food cans. Environ. Health. Persphect., 103, 608-612 https://doi.org/10.2307/3432439
  4. Cagen, S.Z., Waechoter, J.M. Dimond, S.S., Breslin, W.J., Butala, J.H., Jekat, F.W., Joiner, R.L., Shiotsuka, R.N., Veenstra, G.E. and Harris, L.R. (1999): Normal reproductive organ develoment in CF-1 mice following prenatal exposure to bisphenol A. Toxico. Sciences, 50, 36-44 https://doi.org/10.1093/toxsci/50.1.36
  5. Charles, A.S., Philip, B.D., Gary, M.K., Sondra, T. and Lynne, R.H. (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
  6. Colerangle, J.B. and Roy, D. (1997): Profound effects of the weak environmental estrogen-like chemical bisphenol A on the growth of the mammary gland of Noble rat. J. Steroid. Biochem. Mol. Biol., 60, 153-160 https://doi.org/10.1016/S0960-0760(96)00130-6
  7. Cupta, C. (2000): Reproductive malformation of the male offspring following maternal exposure to estrogenic chemicals. Proc. Soc. Exp. Biol. Med., 224, 61-68 https://doi.org/10.1046/j.1525-1373.2000.22402.x
  8. Dodds, E.C. and Lawson, W. (1936): Synthetic oestrogenic agents without the phenanthrene nucleus. Nature, 137, 996 https://doi.org/10.1038/137996a0
  9. Gaido, K.W., L. Leonard, S., Gould, J.C., Babai, D.C., Portier, J. and McDonnell, D.P. (1997): Evaluation of chemicals with endocrine modulating activity in a yeast-based steroid hormone receptor gene transcription assay. Toxicol. Appl. Pharmacol., 143, 205-212 https://doi.org/10.1006/taap.1996.8069
  10. Kuiper, G.G., Carlsson, B., Grandien, K., Enmark, E., Haggblad, J., Nilsson, S. and Gustafson, J.A. (1997): Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors a and B. Endocrinology, 138, 863-870 https://doi.org/10.1210/en.138.3.863
  11. Kwon, S., Stedman, D.B., Elswick, B.A., Cattley, R.C. and Welsch, F. (2000): Pubertal development and reproductive functions of Cr1:CD BR Sprague-Dawley rats exposed to bisphenol A during prenatal and postnatal development. Toxicol. Sci., 55, 399-406 https://doi.org/10.1093/toxsci/55.2.399
  12. Lazear, N.R. (1995): Polycarbonate : high-performance resin. Advmaterial and Processes. 147, 43-45
  13. Magure, H.C. (1998): Experimental photoallergic contant dermatits to bisphenol A. Acta. Derm. Venereol., 68, 408-412
  14. Muldoon, T.G. (1981): Interplay between estradiol and prolactin in the regilation of steroid hormone receptor levels, nature and functionality in normal mouse mammary tissue. Endocrinology, 109, 1339-1346 https://doi.org/10.1210/endo-109-5-1339
  15. Papaconstantinou, A.D., Umbreit, T.H., Fisher, B.R., Goering, P.L., Lappas, N.T. and Brown, K.M. (2000): Bisphenol Ainduced increace in uterine weight and alterations in uterine morphology in ovariectomized B6C3F1 mice : role of the estrogen receptor. Toxicol. Sciences, 56, 332-339 https://doi.org/10.1093/toxsci/56.2.332
  16. Sharpe, R.M., Majdic, G., Fisher, J., Parte, P., Millar, M.R. and Saunders, P.T.K. (1996): Effects on testicular development and function. Int. Congress. Endocrinol., pp. 23-24
  17. Staples, C.A., Dorn, P.B., Klecka, G.M., O'Block, S.T. and Harris, L.R. (1998): A review of the environmental fate: effects and exposures of biapnenol A. Chemosphere, 36, 2149-2173 https://doi.org/10.1016/S0045-6535(97)10133-3
  18. Takai, Y., Tsutsumi, O., Ikezuki, Y., Hiroi, H., Osuga, Y., Momoeda, M., Yano, T. and Taketani, Y. (2000): Estrogen receptor-mediated effects ofaxenoestrogen, biaphenol A, on preimplantation mouse embryos. Biochem. Biophy Reser. Commun., 270, 918-921 https://doi.org/10.1006/bbrc.2000.2548
  19. vom Saal, F.S., Cooke, P.S., Buchanan, D., Palanza, P., Thayer, U.A., Nagai, S.C., Parmigiani, S. and Welshons, W. (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 https://doi.org/10.1177/074823379801400115
  20. 김용배, 박동헌, 박춘근, 김정익, 정희태, 양부근. (2002): 자기장이 웅성생쥐의 정액성상과 장기무게에 미치는 영향. 한국가축번식학회, 26, 53-59