Steroid levels in crinoid echinoderms are altered by exposure to model endocrine disruptors

Steroids

Volumn 71, Issue 6, 2006, Pages 489-497

  Lavado, Ramón ^a   Barbaglio, Alice ^b   Carnevali, M Daniela Candia ^b   Porte, Cinta ^a  

^a DEPARTMENT OF ENVIRONMENTAL CHEMISTRY   (Spain)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

17 Estradiol; Androgenic; Antedon mediterranea; Anti androgenic; Endocrine disruption; Testosterone

Indexed keywords

ANTIANDROGEN; CYPROTERONE ACETATE; ENDOCRINE DISRUPTOR; ESTRADIOL; FENARIMOL; METHYLTESTOSTERONE; TESTOSTERONE; TRIPHENYLTIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUTUMN; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DOSE RESPONSE; ECHINODERM; ESTRADIOL BLOOD LEVEL; FEMALE; ITALY; MALE; NONHUMAN; SEASON; SEX DIFFERENCE; STEROID BLOOD LEVEL; TESTOSTERONE BLOOD LEVEL; TISSUE LEVEL; VERTEBRATE;

ANDROGEN ANTAGONISTS; ANIMALS; CYPROTERONE ACETATE; DICHLORODIPHENYL DICHLOROETHYLENE; DOSE-RESPONSE RELATIONSHIP, DRUG; ECHINODERMATA; ENDOCRINE DISRUPTORS; ENVIRONMENTAL EXPOSURE; ESTRADIOL; FEMALE; MALE; METHYLTESTOSTERONE; ORGANOTIN COMPOUNDS; PYRIMIDINES; STEROIDS; TESTOSTERONE; TIME FACTORS;

ANIMALIA; ANTEDON MEDITERRANEA; ECHINODERMATA; VERTEBRATA;

EID: 33646162659     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2006.01.009     Document Type: Article

References (59)

1. Hines G.A., Watts S.A., Sower S.A., and Walker C.W. Sex steroid levels in the testes, ovaries and pyloric caeca during gametogenesis in the sea star Asterias vulgaris. Gen Comp Endocrinol 87 (1992) 451-460
2. Lafont R. The endocrinology of invertebrates. Ecotoxicology 9 (2000) 41-57
3. Watts S.A., Hines G.A., Byrum C.A., McClintok J.B., Marion K.R., and Hopkins T.S. Tissue- and species-specific variations in androgen metabolism. In: Davi, Guille, Feral, and Roux (Eds). Echinoderms through time (1994), Balkema, Rotterdam, Netherlands 155-161
4. Voogt P.A., Lambert J.G.D., Granneman J.C.M., and Jansen M. Confirmation of the presence of oestradiol-17β in sea star Asterias rubens by GC-MS. Comp Biochem Physiol 101B (1992) 13-16
5. Wasson K.M., Gower B.A., Hines G.A., and Watts S.A. Levels of progesterone, testosterone and estradiol and androstenedione metabolism in the gonads of Lytechinus variegatus (Echinodermata: Echinoidea). Comp Biochem Physiol 126C (2000) 153-165
6. Wasson K.M., Hines G.A., and Watts S.A. Synthesis of testosterone and 5α-androstanediols during nutritionally stimulated gonadal growth in Lytechinus variegatus L. (Echinodermata: Echinoidea). Gen Comp Endocrinol 111 (1998) 197-206
7. Schoenmakers H.J.N. In vitro biosynthesis of steroids from cholesterol by the ovaries and pyloric caeca of the starfish Asterias rubens. Comp Biochem Physiol 63B (1979) 179-184
8. Voogt P.A., den Besten P.J., and Jansen M. Steroid metabolism in relation to the reproductive cycle in Asterias rubens L. Comp Biochem Physiol. 99B (1991) 77-82
9. Voogt P.A., and Dieleman J.S. Progesterone and oestrone levels in the gonads and pyloric caeca of the male sea star Asterias rubens: a comparison with the corresponding levels in the female sea star. Comp Biochem Physiol 79A (1984) 635-639
10. Xu R.A., and Barker M.F. Annual changes in the steroid levels in the ovaries and the pyloric caeca of Sclerasterias mollis during the reproductive cycle. Comp Biochem Physiol. 95A (1990) 127-133
11. Barbaglio A, Mozzi D, Sugni M, Tremolada P, Lavado R, Porte C, et al. Effects of exposure to ED contaminants (TPT-Cl and Fenarimol) on crinoid echinoderms: comparative analysis of regenerative development and correlated steroid levels. Mar Biol, in press.
12. Voogt P.A., den Besten P.J., Kusters G.C.M., and Messing M.W.J. Effects of cadmium and zinc on steroid metabolism and steroid level in the sea star Asterias rubens L. Comp Biochem Physiol 86C (1987) 83-89
13. den Besten P.J., Elenbaas J.M., Maas E.J.R., Dielman S.J., Herwig H.J., and Voogt P.A. Effects of cadmium and polychlorinated biphenyls (Clophen A50) on steroid metabolism and cytochrome P-450 monooxigenase system in the sea star Asterias rubens L. Aquat Toxicol 20 (1991) 95-110
14. den Besten P.J., Herwig H.J., Smaal A.C., Zandee D.I., and Voogt P.A. Interference of polychlorinated biphenyls (Clophen A50) with gametogenesis in the sea star Asterias rubens L. Aquat Toxicol 18 (1990) 231-246
15. den Besten P.J., Herwig H.J., Zandee D.I., and Voogt P.A. Effects of cadmium and PCBs on reproduction of the sea star Asterias rubens: aberrations in the early development. Ecotoxicol Environ Saf 18 (1989) 173-180
16. Khristoforova N.K., Gnezdilova S.M., and Vlasova G.A. Effects of cadmium on gametogenesis and offspring of the sea urchin Strongylocentrotus intermedius. Mar Ecol Prog Ser 17 (1984) 9-14
17. Walsh G.E., McLaughlin L.L., Louie M.K., Deans C.H., and Lores E.M. Inhibition of arm regeneration by Ophioderma brevispina (Echinodermata, Ophiuroidea) by tributyltin oxide and triphenyltin oxide. Ecotoxicol Environ Saf 12 (1986) 95-100
18. Candia Carnevali M.D., Bonasoro F., Patruno M., Thorndyke M.C., and Galassi S. PCB exposure and regeneration in crinoids (Echinodermata). Mar Ecol Prog Ser 215 (2001) 155-167
19. Candia Carnevali M.D., Bonasoro F., Ferreri P., and Galassi S. Regenerative potential and effects of exposure to pseudo-estrogenic contaminants (4-nonylphenol) in the crinoid Antedon mediterranea. In: Feral J.P. (Ed). Echinoderm Research 2001 (2003), Balkema, Rotterdam, Netherlands 201-207
20. Hunter G.A., and Donaldson E.M. Hormonal sex control and its application to fish culture. In: Hoar W.S., Randall D.J., and Donaldson E.M. (Eds). Fish Physiology. Part B. Behaviour and fertility control, vol. IX (1983), Academic Press, New York 223-303
21. Morcillo Y., Albalat A., and Porte C. Mussels as sentinels of organotin pollution: bioaccumulation and effects on P450-mediated aromatase activity. Environ Toxicol Chem 18 (1999) 1203-1208
22. Golub M.S., and Doherty J.D. Triphenyltin as a potential human endocrine disruptor. J Toxicol Environ Health B: Crit Rev 7 (2004) 281-295
23. Hirsch K.S., Weaver D.E., Black L.J., Falcone J.F., and MacLusky N.J. Inhibition of central nervous system aromatase activity: a mechanism for fenarimol-induced infertility in the male rat. Toxicol Appl Pharmacol 91 (1987) 235-245
24. Amory J.K., and Bremner W.J. Newer agents for hormonal contraception in the male. Trends Endocrinol Metab 11 (2000) 61-66
25. Porte C., Escartín E., García de la Parra L.M., Biosca X., and Albaigés J. Assessment of coastal pollution by combined determination of chemical and biochemical markers in Mullus barbatus. Mar Ecol Prog Ser 235 (2002) 205-216
26. Kelce W.R., Stone C.R., Laws S.C., Gray L.E., Kemppainen J.A., and Wilson E.M. Persistent DDT metabolite p,p′-DDE is a potent androgen receptor antagonist. Nature 375 (1995) 581-585
27. Candia Carnevali M.D., Lucca E., and Bonasoro F. Mechanism of arm regeneration in the feather star Antedon mediterranea: healing of wound and early stages of development. J Exp Zool 267 (1993) 299-317
28. Janer G., Lavado R., Thibaut R., and Porte C. Effects of 17β-Estradiol exposure in the mussel Mytilus galloprovincialis: the regulating role of steroid acyltransferases. Aquat Toxicol 75 (2005) 32-42
29. Morcillo Y., Borghi V., and Porte C. Survey of organotin compounds in the western Mediterranean using molluscs and fish as sentinel organisms. Arch Environ Contam Toxicol. 32 (1997) 198-203
30. Holland N.D. Echinodermata: Crinoidea. In: Giese A.C., Pearse J.S., and Pearse V.B. (Eds). Reproduction of marine invertebrates. Echinoderms and lophophorates, vol. VI (1991), Boxwood Press, Pacific Grove 247-301
31. Walker C.W. Nutrition of gametes. In: Jangoux M., and Lawrence J.M. (Eds). Echinoderm nutrition (1982), Balkema, Rotterdam 449-469
32. Pearse J.S., and Cameron R.A. Echinodermata: Echinoidea. In: Giese A.C., Pearse J.S., and Pearse V.B. (Eds). Reproduction of marine invertebrates. Echinoderms and lophophorates, vol. VI (1991), Boxwood Press, Pacific Grove 514-664
33. Holland N.D., and Kubota H. Correlated scanning and transmission electron-microscopy of larvae of feather star Comanthus japonica (Echinodermata: Crinoidea). Trans Am Microscop Soc 94 (1975) 58-70
34. Wasson K.M., and Watts S.A. Progesterone metabolism in the ovaries and testes of the echinoid Lytechinus variegatus L. (Echinodermata). Comp Biochem Physiol 127C (2000) 263-272
35. Chang C.F., Hung C.Y., Chiang M.C., and Lan S.C. The concentrations of plasma sex steroids and gonadal aromatase during controlled sex differentiation in grey mullet, Mugil cephalus. Aquaculture 177 (1999) 37-45
36. Yeh S.L., Kuo C.M., Ting Y.Y., and Chang C.F. The effects of exogenous androgens on ovarian development and sex change in female orange-spotted protogynous grouper, Epinephelus coioides. Aquaculture 218 (2003) 729-739
37. Fait A., Ferioli A., and Barbieri F. Organotin compounds. Toxicology 91 (1994) 77-82
38. Moschino V., and Marin M. Spermiotoxicity and embriotoxicity of triphenyltin in the sea urchin Paracentrotus lividus L. Appl Organometal Chem 16 (2002) 175-181
39. Paolini M., Mesirca R., Pozzetti L., Sapone A., and Castelli-Forti G. Molecular non-genetic biomarkers related to fenarimol cocarcinogenesis: Organ- and sex-specific CYP induction in rat. Cancer Lett 101 (1996) 171-178
40. Mason J.I., Carr B.R., and Murry B.A. Imidazole antimycotics: selective inhibitors of steroid aromatization and progesterone hydroxylation. Steroids 50 (1987) 179-189
41. Vinggaard A.M., Hnida C., Breinholt V., and Larsen J.C. Screening of selected pesticides for inhibition of CYP19 aromatase activity in vitro. Toxicol In-Vitro 14 (2000) 227-234
42. Andersen H.R., Vingaard A.M., Rasmussen T.H., Gjermandsen I.M., and Bonefeld-Jørgensen E.C. Effects of currently used pesticides in assays for estrogenicity, androgenicity and aromatase activity in vitro. Toxicol Appl Pharmacol 179 (2002) 1-12
43. Kojima H., Katsura E., Takeuchi S., Niiyama K., and Kobayashi K. Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells. Environ Health Perspect 112 (2004) 524-531
44. Vinggaard A.M., Jacobsen H., Metzdorff S.B., Andersen H.R., and Nellemann C. Anti-androgenic affects in short-term in vivo studies of the fungicide fenarimol. Toxicology 207 (2005) 21-34
45. Lorenzo J. A new hypothesis for how sex steroid hormones regulate bone mass. J Clin Invest 111 (2003) 1641-1643
46. Heinzeller T., and Welsch U. Crinoidea. In: Herrison F. (Ed). Microscopic anatomy of invertebrates. Echinodermata, vol. 14 (1994), Wiley-Liss, New York 9-148
47. Wells K.L., and Van der Kraak G.J. Differential binding of endogenous steroids and environmental chemicals to androgen receptor in rainbow trout and goldfish. Environ Toxicol Chem. 19 (2000) 2059-2065
48. Sharpe R.L., MacLathy D.L., Courtenay S.C., and Van der Kraak G.J. Effects of a model androgen (methyltestosterone) and a model anti-androgen (cyproterone acetate) on reproductive endocrine endpoints in a short-term adult mummichog (Fundulus heteroclitus) bioassay. Aquat Toxicol 67 (2004) 203-215
49. Kiparissis Y., Metcalfe T.L., Balch G.C., and Metcalfe C.R. Effects of the antiandrogens, vinclozolin and cyproterone acetate on gonadal development in the Japanese medaka (Oryzias latipes). Aquat Toxicol 63 (2003) 391-403
50. Singh M.S., and Joy K.P. Effects of administration of cyproterone acetate on seminal vesicle and testicular activity, and serum testosterone and estradiol-17β levels in the catfish, Clarias batrachus. Acta Biologica 49 (1998) 143-154
51. Tillmann M., Schulte-Oehlmann U., Duft M., Markert B., and Oehlmann J. Effects of endocrine disruptors on prosobranch snails (Mollusca: Gastropoda) in the laboratory. Part III. Cyproterone acetate and vinclozolin as antiandrogens. Ecotoxicology 10 (2001) 373-388
52. Loomis A.K., and Thomas P. Binding characteristics of estrogen receptor (ER) in Atlantic croaker (Micropogonias undulatus) testis: different affinity for estrogens and xenobiotics from that of hepatic ER. Biol Reprod 61 (1999) 51-60
53. Mills L.J., Gutjahr-Gobell R.E., Haebler R.A., Borsay Horowitz D.J., Jayaraman S., Pruell R.J., et al. Effects of estrogenic (o,p′-DDT; octylphenol) and anti-androgenic (p,p′-DDE) chemicals on indicators of endocrine status in juvenile male summer flounder (Paralichthys dentatus). Aquat Toxicol 52 (2001) 157-176
54. Gooding M.P., and LeBlanc G.A. Biotransformation and disposition of testosterone in the eastern mud snail Ilyanassa obsolete. Gen Comp Endocrinol 122 (2001) 172-180
55. Janer G., Sternberg R.M., LeBlanc G.A., and Porte C. Testosterone conjugating activities in invertebrates: are they targets for endocrine disruptors?. Aquat Toxicol 71 (2005) 273-282
56. Voogt P.A., and Rheenen W.A. Androstenedione metabolism in the sea star Asterias rubens L. studied in homogenates and intact tissue: biosynthesis of the novel steroid fatty-acyl testosterone. Comp Biochem Physiol 2B (1986) 497-501
57. Voogt P.A., den Besten P.J., and Jansen M. The Δ5-pathway in steroid metabolism in the sea star Asterias rubens L. Comp Biochem Physiol 97B (1990) 555-562
58. Tremolada P, Mozzi D, Sugni M, Barbaglio A, Dagnac T, Candia Carnevali MD. A simple model to predict compound loss processes in aquatic ecotoxicological tests: calculated and measured TPT-Cl levels in water and biota. Int J Environ Anal Chem, in press.
59. Tolosa I., Readman J.W., Blaevoet A., Ghilini S., Bartocci J., and Horvat M. Contamination of Mediterranean (Côte d'Azur) coastal waters by organotins and Irgarol 1051 used in antifouling paints. Mar Pollut Bull 32 (1996) 335-341