Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 1995 May;103(Suppl 4):31–36. doi: 10.1289/ehp.95103s431

Gonadal steroidogenesis in vitro from juvenile alligators obtained from contaminated or control lakes.

L J Guillette Jr 1, T S Gross 1, D A Gross 1, A A Rooney 1, H F Percival 1
PMCID: PMC1519267  PMID: 7556021

Abstract

The ubiquitous distribution of many contaminants and the nonlethal, multigenerational effects of such contaminants on reproductive, endocrine, and immune systems have led to concerns that wildlife worldwide are affected. Although the causal agents and effects are known for some species, the underlying physiological mechanisms associated with contaminant-induced reproductive modifications are still poorly understood and require extensive research. We describe a study examining the steroidogenic activity of gonads removed from juvenile alligators (Alligator mississippiensis) obtained from contaminated or control lakes in central Florida. Synthesis of estradiol-17 beta (E2) was significantly different when ovaries from the contaminated and control lakes were compared in vitro. Additionally, testes from males obtained from the contaminated lake. Lake Apopka, synthesized significantly higher concentrations of E2 when compared to testes obtained from control males. In contrast, testosterone (T) synthesis from all testes examined in this study displayed a normal pattern and produced concentrations greater than that observed from ovaries obtained from either lake. Interestingly, the pattern of gonadal steroidogenesis differs from previously reported plasma concentrations of these hormones obtained from the same individuals. We suggest that the differences between the in vivo and in vitro patterns are due to modifications in the hepatic degradation of plasma sex steroid hormones.

Full text

PDF
31

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Braux J. P., Dufaure J. P. Particularité de la liaison de la testostérone aux protéines plasmatiques au cours du cycle sexuel chez un animal à reproduction saisonnière, le lézard vivipare mâle. C R Seances Acad Sci III. 1983 Jan 10;296(1):59–62. [PubMed] [Google Scholar]
  2. Bulger W. H., Kupfer D. Estrogenic action of DDT analogs. Am J Ind Med. 1983;4(1-2):163–173. [PubMed] [Google Scholar]
  3. 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]
  4. Corvol P., Bardin C. W. Species distribution of testosterone-binding globulin. Biol Reprod. 1973 Apr;8(3):277–282. doi: 10.1093/biolreprod/8.3.277. [DOI] [PubMed] [Google Scholar]
  5. DiBartolomeis M. J., Moore R. W., Peterson R. E., Christian B. J., Jefcoate C. R. Altered regulation of adrenal steroidogenesis in 2,3,7,8-tetrachlorodibenzo-p-dioxin-treated rats. Biochem Pharmacol. 1987 Jan 1;36(1):59–67. doi: 10.1016/0006-2952(87)90382-0. [DOI] [PubMed] [Google Scholar]
  6. DiBartolomeis M. J., Moore R. W., Peterson R. E., Jefcoate C. R. Hypercholesterolemia and the regulation of adrenal steroidogenesis in 2,3,7,8-tetrachlorodibenzo-p-dioxin-treated rats. Toxicol Appl Pharmacol. 1986 Sep 30;85(3):313–323. doi: 10.1016/0041-008x(86)90338-8. [DOI] [PubMed] [Google Scholar]
  7. Faber K. A., Basham K., Hughes C. L., Jr The effect of neonatal exposure to DES and o,p'-DDT on pituitary responsiveness to GnRH in adult castrated rats. Reprod Toxicol. 1991;5(4):363–369. doi: 10.1016/0890-6238(91)90095-w. [DOI] [PubMed] [Google Scholar]
  8. Guillette L. J., Jr, Gross T. S., Masson G. R., Matter J. M., Percival H. F., Woodward A. R. Developmental abnormalities of the gonad and abnormal sex hormone concentrations in juvenile alligators from contaminated and control lakes in Florida. Environ Health Perspect. 1994 Aug;102(8):680–688. doi: 10.1289/ehp.94102680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Haake J., Kelley M., Keys B., Safe S. The effects of organochlorine pesticides as inducers of testosterone and benzo[a]pyrene hydroxylases. Gen Pharmacol. 1987;18(2):165–169. doi: 10.1016/0306-3623(87)90244-8. [DOI] [PubMed] [Google Scholar]
  10. Hose J. E., Guillette L. J. Defining the role of pollutants in the disruption of reproduction in wildlife. Environ Health Perspect. 1995 May;103 (Suppl 4):87–91. doi: 10.1289/ehp.95103s487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Khan M. S., Knowles B. B., Aden D. P., Rosner W. Secretion of testosterone-estradiol-binding globulin by a human hepatoma-derived cell line. J Clin Endocrinol Metab. 1981 Aug;53(2):448–449. doi: 10.1210/jcem-53-2-448. [DOI] [PubMed] [Google Scholar]
  12. Martin B., Xavier F. High-affinity binding of progesterone, estradiol-17 beta and testosterone by plasma proteins of the reptile Lacerta vivipara J. Gen Comp Endocrinol. 1981 Mar;43(3):299–307. doi: 10.1016/0016-6480(81)90288-4. [DOI] [PubMed] [Google Scholar]
  13. McLachlan J. A. Functional toxicology: a new approach to detect biologically active xenobiotics. Environ Health Perspect. 1993 Oct;101(5):386–387. doi: 10.1289/ehp.93101386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Moore R. W., Jefcoate C. R., Peterson R. E. 2,3,7,8-Tetrachlorodibenzo-p-dioxin inhibits steroidogenesis in the rat testis by inhibiting the mobilization of cholesterol to cytochrome P450scc. Toxicol Appl Pharmacol. 1991 Jun 1;109(1):85–97. doi: 10.1016/0041-008x(91)90193-i. [DOI] [PubMed] [Google Scholar]
  15. Salhanick A. C., Callard I. P. A sex-steroid-binding protein in the plasma of the freshwater turtle, Chrysemys picta. Gen Comp Endocrinol. 1980 Oct;42(2):163–166. doi: 10.1016/0016-6480(80)90183-5. [DOI] [PubMed] [Google Scholar]
  16. Salhanick A. R., Vito C. C., Fox T. O., Callard I. P. Estrogen-binding proteins in the oviduct of the turtle, Chrysemys picta: evidence for a receptor species. Endocrinology. 1979 Dec;105(6):1388–1395. doi: 10.1210/endo-105-6-1388. [DOI] [PubMed] [Google Scholar]
  17. Takamatsu Y., Iguchi T., Takasugi N. Effects of neonatal exposure to diethylstilbestrol on protein expression by vagina and uterus in mice. In Vivo. 1992 Jan-Feb;6(1):1–8. [PubMed] [Google Scholar]
  18. Uchima F. D., Vallerga A. K., Firestone G. L., Bern H. A. Effects of early exposure to diethylstilbestrol on cellular protein expression by mouse vaginal epithelium and fibromuscular wall. Proc Soc Exp Biol Med. 1990 Nov;195(2):218–223. doi: 10.3181/00379727-195-43138. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES