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. 1995 Oct;103(Suppl 7):173–178. doi: 10.1289/ehp.95103s7173

Vitellogenesis as a biomarker for estrogenic contamination of the aquatic environment.

J P Sumpter 1, S Jobling 1
PMCID: PMC1518861  PMID: 8593867

Abstract

A rapidly increasing number of chemicals, or their degradation products, are being recognized as possessing estrogenic activity, albeit usually weak. We have found that effluent from sewage treatment works contains a chemical, or mixture of chemicals, that induces vitellogenin synthesis in male fish maintained in the effluent, thus indicating that the effluent is estrogenic. The effect was extremely pronounced and occurred at all sewage treatment works tested. The nature of the chemical or chemicals causing the effect is presently not known. However, we have tested a number of chemicals known to be estrogenic to mammals and have shown that they are also estrogenic to fish; that is, no species specificity was apparent. Many of these weakly estrogenic chemicals are known to be present in effluents. Further, a mixture of different estrogenic chemicals was considerably more potent than each of the chemicals when tested individually, suggesting that enhanced effects could occur when fish are exposed simultaneously to various estrogenic chemicals (as is likely to occur in rivers receiving effluent). Subsequent work should determine whether exposure to these chemicals at the concentrations present in the environment leads to any deleterious physiological effects.

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Selected References

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  1. Ahel M., McEvoy J., Giger W. Bioaccumulation of the lipophilic metabolites of nonionic surfactants in freshwater organisms. Environ Pollut. 1993;79(3):243–248. doi: 10.1016/0269-7491(93)90096-7. [DOI] [PubMed] [Google Scholar]
  2. Aherne G. W., Briggs R. The relevance of the presence of certain synthetic steroids in the aquatic environment. J Pharm Pharmacol. 1989 Oct;41(10):735–736. doi: 10.1111/j.2042-7158.1989.tb06355.x. [DOI] [PubMed] [Google Scholar]
  3. Campbell P. M., Pottinger T. G., Sumpter J. P. Changes in the affinity of estrogen and androgen receptors accompany changes in receptor abundance in brown and rainbow trout. Gen Comp Endocrinol. 1994 Jun;94(3):329–340. doi: 10.1006/gcen.1994.1089. [DOI] [PubMed] [Google Scholar]
  4. Carnevali O., Mosconi G., Yamamoto K., Kobayashi T., Kikuyama S., Polzonetti-Magni A. M. Hormonal control of in vitro vitellogenin synthesis in Rana esculenta liver: effects of mammalian and amphibian growth hormone. Gen Comp Endocrinol. 1992 Dec;88(3):406–414. doi: 10.1016/0016-6480(92)90235-c. [DOI] [PubMed] [Google Scholar]
  5. Carnevali O., Mosconi G., Yamamoto K., Kobayashi T., Kikuyama S., Polzonetti-Magni A. M. In-vitro effects of mammalian and amphibian prolactins on hepatic vitellogenin synthesis in Rana esculenta. J Endocrinol. 1993 Jun;137(3):383–389. doi: 10.1677/joe.0.1370383. [DOI] [PubMed] [Google Scholar]
  6. Carragher J. F., Sumpter J. P., Pottinger T. G., Pickering A. D. The deleterious effects of cortisol implantation on reproductive function in two species of trout, Salmo trutta L. and Salmo gairdneri Richardson. Gen Comp Endocrinol. 1989 Nov;76(2):310–321. doi: 10.1016/0016-6480(89)90163-9. [DOI] [PubMed] [Google Scholar]
  7. Colborn T., vom Saal F. S., Soto A. M. Developmental effects of endocrine-disrupting chemicals in wildlife and humans. Environ Health Perspect. 1993 Oct;101(5):378–384. doi: 10.1289/ehp.93101378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Copeland P. A., Sumpter J. P., Walker T. K., Croft M. Vitellogenin levels in male and female rainbow trout (Salmo gairdneri Richardson) at various stages of the reproductive cycle. Comp Biochem Physiol B. 1986;83(2):487–493. doi: 10.1016/0305-0491(86)90400-1. [DOI] [PubMed] [Google Scholar]
  9. Ekelund R., Bergman A., Granmo A., Berggren M. Bioaccumulation of 4-nonylphenol in marine animals--a re-evaluation. Environ Pollut. 1990;64(2):107–120. doi: 10.1016/0269-7491(90)90108-o. [DOI] [PubMed] [Google Scholar]
  10. Guillette L. J., Jr, Crain D. A., Rooney A. A., Pickford D. B. Organization versus activation: the role of endocrine-disrupting contaminants (EDCs) during embryonic development in wildlife. Environ Health Perspect. 1995 Oct;103 (Suppl 7):157–164. doi: 10.1289/ehp.95103s7157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hyllner S. J., Oppen-Berntsen D. O., Helvik J. V., Walther B. T., Haux C. Oestradiol-17 beta induces the major vitelline envelope proteins in both sexes in teleosts. J Endocrinol. 1991 Nov;131(2):229–236. doi: 10.1677/joe.0.1310229. [DOI] [PubMed] [Google Scholar]
  12. Krishnan A. V., Stathis P., Permuth S. F., Tokes L., Feldman D. Bisphenol-A: an estrogenic substance is released from polycarbonate flasks during autoclaving. Endocrinology. 1993 Jun;132(6):2279–2286. doi: 10.1210/endo.132.6.8504731. [DOI] [PubMed] [Google Scholar]
  13. Le Roux M. G., Thézé N., Wolff J., Le Pennec J. P. Organization of a rainbow trout estrogen receptor gene. Biochim Biophys Acta. 1993 Feb 20;1172(1-2):226–230. doi: 10.1016/0167-4781(93)90302-t. [DOI] [PubMed] [Google Scholar]
  14. Pakdel F., Le Gac F., Le Goff P., Valotaire Y. Full-length sequence and in vitro expression of rainbow trout estrogen receptor cDNA. Mol Cell Endocrinol. 1990 Jul 9;71(3):195–204. doi: 10.1016/0303-7207(90)90025-4. [DOI] [PubMed] [Google Scholar]
  15. Parker M. G. Mortyn Jones Memorial Lecture. Structure and function of the oestrogen receptor. J Neuroendocrinol. 1993 Jun;5(3):223–228. doi: 10.1111/j.1365-2826.1993.tb00476.x. [DOI] [PubMed] [Google Scholar]
  16. Pelissero C., Flouriot G., Foucher J. L., Bennetau B., Dunoguès J., Le Gac F., Sumpter J. P. Vitellogenin synthesis in cultured hepatocytes; an in vitro test for the estrogenic potency of chemicals. J Steroid Biochem Mol Biol. 1993 Mar;44(3):263–272. doi: 10.1016/0960-0760(93)90086-c. [DOI] [PubMed] [Google Scholar]
  17. Pottinger T. G. Estrogen-binding sites in the liver of sexually mature male and female brown trout, Salmo trutta L. Gen Comp Endocrinol. 1986 Jan;61(1):120–126. doi: 10.1016/0016-6480(86)90256-x. [DOI] [PubMed] [Google Scholar]
  18. Rabelo E. M., Tata J. R. Thyroid hormone potentiates estrogen activation of vitellogenin genes and autoinduction of estrogen receptor in adult Xenopus hepatocytes. Mol Cell Endocrinol. 1993 Oct;96(1-2):37–44. doi: 10.1016/0303-7207(93)90092-x. [DOI] [PubMed] [Google Scholar]
  19. Scott A. P., Sumpter J. P. A comparison of the female reproductive cycles of autumn-spawning and winter-spawning strains of rainbow trout (Salmo gairdneri Richardson). Gen Comp Endocrinol. 1983 Oct;52(1):79–85. doi: 10.1016/0016-6480(83)90160-0. [DOI] [PubMed] [Google Scholar]
  20. Soto A. M., Justicia H., Wray J. W., Sonnenschein C. p-Nonyl-phenol: an estrogenic xenobiotic released from "modified" polystyrene. Environ Health Perspect. 1991 May;92:167–173. doi: 10.1289/ehp.9192167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Sumpter J. P., Jobling S. Male sexual development in "a sea of oestrogen". Lancet. 1993 Jul 10;342(8863):124–125. [PubMed] [Google Scholar]
  22. White R., Jobling S., Hoare S. A., Sumpter J. P., Parker M. G. Environmentally persistent alkylphenolic compounds are estrogenic. Endocrinology. 1994 Jul;135(1):175–182. doi: 10.1210/endo.135.1.8013351. [DOI] [PubMed] [Google Scholar]

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