Effects of Bisphenol A on Sex Differentiation and Gonadal Development of Medaka, Oryzias latipes

  • Na, Oh-Soo (Marine and Environmental Research Institute, Cheju National University) ;
  • Lee, Young-Don (Marine and Environmental Research Institute, Cheju National University) ;
  • Baek, Hea-Ja (Combined Departments of Fisheries Marine Life Science, Pukyong National University) ;
  • Kim, Hyung-Bae (Department of Marine Biotechnology, Kangwon Provincial University)
  • Published : 2002.03.01

Abstract

A study on the effects of bisphenol A (BPA) on sex differentiation and gonadal development in medaka, Oryzias latipes, was investigated by histological examination. The fish were exposed to aqueous solutions of BPA at nominal concentrations of 50, 100, and 200 $\mu\textrm{g}$/L from newly-hatched larvae stage to 70 d. The ovaries of female fish were composed of oocytes at the chromatin nucleolus and peri-nucleolus stages at 20 d after the exposure. The testes contained a number of spermatogonia and spermatocytes at 30 d. In the process of sex differentiation. gonadal development was not different in all experimental groups until 30 d after the exposure. At 70 d after the exposure, however, advanced development of oocytes in the ovary and inhibition of spermatogenesis in the testis were observed in the BPA-treated groups compared to the non-treated controls. More females than males were identified in the 50 and 100 $\mu\textrm{g}$/L BPA-treated groups, in comparison to the 200 $\mu\textrm{g}$/L BPA-treated group and non-treated controls. Medaka exposed to 200 $\mu\textrm{g}$/L BPA were bigger compared to other experimental groups. The present study suggests that BPA may lead to problems in either mating or sexual behavior due to the difference in growth and disparity of sexual maturation between male and female fish.

Keywords

References

  1. Brotons JA, Olea SMF, Villalobos M, Pedraza V, and Olea N (1995) Xenoestrogens released from lacquer coatings in food can. Environ Health Perspect 103: 608-612 https://doi.org/10.2307/3432439
  2. Christiansen T, Korsgaaard B, and Jespersen A (1998a) Induction of vitellogenin synthesis by nonylphenol and $17{\beta}-estradiol$ and effect on the testicular structure in the eelpout Zoarces viviparus. Mar Environ Res 46: 141-144 https://doi.org/10.1016/S0141-1136(97)00046-9
  3. Christiansen T, Korsgaaard B, and Jespersen A (1998b) Effects of nonylphenol and $17{\beta}-estradiol$ on vitellogenin synthesis, testicular structure and cytology in male eelpout Zoarces viviparus. J Exp Biol 201: 179-192
  4. Colombo G and Grandi G (1995) Sex differentiation in the European eel: histological analysis of the effects of sex steroids on the gonad. J Fish Biol 47: 394-413 https://doi.org/10.1111/j.1095-8649.1995.tb01909.x
  5. Dimond SS, Waechter JM Jr, Breslin WJ, Butala JH, Cagen SZ, Jekat FW, Joiner RL, Shiotsuka RN, and Veenstra GE (1998) Evaluation of reproductive organ development in the male offspring of female Wistar rats exposed to bisphenol A in the drinking water. Unpublished study of the Society of the Plastics Industry Inc. and the European Chemical Industry Council
  6. European Commission (1996) European workshop on the impact of endocrine disruptors on human health and wildlife. Weybridge. Report EUR 17549. Environment and Climate Research Program DG
  7. Foyle TP (1993) A histological description of gonadal development and sex differentiation in the coho salmon (Oncorhynchus kisutch) for both untreated and oestradiol immersed fry. J Fish Biol 42: 699-712 https://doi.org/10.1111/j.1095-8649.1993.tb00379.x
  8. Gray MA and Metcalfe CD (1997) Induction of testis-ova in Japanese medaka (Oryzias latipes) exposed to p-nonylphenol. Environ toxicol Chem 16: 1082-1086 https://doi.org/10.1897/1551-5028(1997)016<1082:IOTOIJ>2.3.CO;2
  9. Grier HJ (1976) Sperm development in the medaka, Oryzias latipes. Cell Tissue Res 168: 419-431 https://doi.org/10.1007/BF00215993
  10. Jobling S, Sheathan D, Osborne JA, Matthiessen P, and Sumpter JP (1996) Inhibition of testicular growth in rainbow trout (Oncorhynchus mykiss) exposed to estrogenic alkylphenolic chemicals. Environ Toxicol Chem 15: 194-202 https://doi.org/10.1897/1551-5028(1996)015<0194:IOTGIR>2.3.CO;2
  11. Malison JA, Kayes TB, Wentworth BC, and Amundson CH (1988) Growth and feeding responses of male versus female yellow perch (Perca flavescens) treated with $17{\beta}-estradiol$. Can J Fish Aquat Sci 45: 1942-1948 https://doi.org/10.1139/f88-226
  12. Metcalfe CD, Metcalfe TL, Kiparissis Y, Koenig BG, Khan C, Hughes RJ, Croley TR, March RE, and Potter T (2001) Estrogenic potency of chemicals detected in sewage treatment plant effluents as determined by in vivo assays with Japanese medaka (Oryzias latipes). Environ Toxicol Chem 20: 297-308 https://doi.org/10.1897/1551-5028(2001)020<0297:EPOCDI>2.0.CO;2
  13. Moon SJ (1999) Effects of Nonylphenol on Reproduction of the Olive Flounder, Paralichthys olivaceus. MS Thesis, Cheju National University Korea. pp 1-34
  14. Olea N, Pulgar R, Perez P, Olea SF, Rivas A, Novillo FA, Pedraza V, Soto AM, and Sonnenschein C (1996) Estrogenicity of resin based composites and sealants used in dentistry. Environ Health Perspect 104: 298-305 https://doi.org/10.2307/3432888
  15. Sharpe RM, Fisher JS, Millar MM, Jobling S, and Sumpter JP (1995) Gestational and lactational exposure of rats to xenoestrogens results in reduced testicular size and sperm production. Environ Health Perspect 103: 1136-1143 https://doi.org/10.2307/3432610
  16. Specker JL and Sullivan G (1994) Vitellogenesis in fishes: status and perspectives. In: Davey KG, Peter RE, and Tobe SS (eds), Perspectives in Comparative Endocrinology. National Research Council of Canada, Ottawa, pp 304-315
  17. Staples CA, Dorn PB, Klecka Gm, OBlock ST, and Harris LR (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
  18. Strussmann CA, Takashima F, and Toda K (1996) Sex differentiation and hormonal feminization in pejerrey Odontesthes bonariensis. Aquaculture 139: 31-45 https://doi.org/10.1016/0044-8486(95)01161-7
  19. Wester PW and Canton JH (1986) Histopathological study of Oryzias latipes (medaka) after long-term ${\beta}-hexachlorochclohexane$ exposure. Aquat Toxicol 9: 21-45 https://doi.org/10.1016/0166-445X(86)90004-4
  20. Yamamoto K and Yoshioka H (1964) Rhythm of development in the oocyte of the medaka, Oryzias latipes. Bull Fac Fish Hokkaido Univ 15: 5-19
  21. Yamamoto T (1969) Sex differentiation. In: Hoar WS and Randall DJ (eds), Fish Physiology III. Academic Press, New York. pp 117-175
  22. Yokota H, Tsuruda Y, Maeda M, Oshima Y, Tadokoro H, Nakazono A, Honjo T, and Kobayashi K (2000) Effect of bisphenol A on the early life stage in Japanese medaka (Oryzias latipes). Environ Toxicol Chem 19: 1925-1930 https://doi.org/10.1897/1551-5028(2000)019<1925:EOBAOT>2.3.CO;2