Effects of anti-androgens cyproterone acetate, linuron, vinclozolin, and p,p'-DDE on the reproductive organs of the copepod Acartia tonsa

J Environ Sci Health A Tox Hazard Subst Environ Eng. 2016 Nov 9;51(13):1111-20. doi: 10.1080/10934529.2016.1199769. Epub 2016 Jul 15.

Abstract

The study was performed to detect the effects of anti-androgenic compounds on the reproduction. In this paper alterations observed in the marine calanoid copepod Acartia tonsa exposed to environmental concentrations of cyproterone acetate (CPA), linuron (LIN), vinclozolin (VIN), and 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (p,p'-DDE) for 21 days covering a full life cycle are described. Histological alterations were studied with a focus on reproductive organs, gonad and accessory sexual glands. Exposure to ≥1.2 µg L(-1) CPA caused degeneration of spermatocytes and deformation of the spermatophore in males. In a single male exposed to 33 µg L(-1) CPA, an ovotestis was observed. In CPA exposed females, enhancement of oogenesis, increase in apoptosis and a decrease in proliferation occurred. Exposure of males to ≥12 µg L(-1) LIN caused degenerative effects in spermatogonia, spermatocytes and spermatids, and at 4.7 µg L(-1) LIN, the spermatophore wall displayed an irregular formation. In LIN exposed females, no such structural alterations were found; however, the proliferation index was reduced at 29 µg L(-1) LIN. At an exposure concentration of ≥100 µg L(-1) VIN, distinct areas in male gonad were stimulated, whereas others displayed a disturbed spermatogenesis and a deformed spermatophore wall. In VIN exposed female A. tonsa, no effects were observed. Male A. tonsa exposed to p,p'-DDE displayed an impairment of spermatogenesis in all stages with increased degrees of apoptosis. In p,p'-DDE-exposed females, a statistical significant increase of the proliferation index and an intensification of oogenesis were observed at 0.0088 µg L(-1).

Keywords: Comparative pathology; crustacea; endocrine disruption; histology; invertebrate.

MeSH terms

  • Androgen Antagonists / toxicity*
  • Animals
  • Copepoda / drug effects*
  • Cyproterone Acetate / toxicity*
  • Dichlorodiphenyl Dichloroethylene / toxicity*
  • Female
  • Gonads / drug effects*
  • Linuron / toxicity*
  • Male
  • Oogenesis / drug effects
  • Oxazoles / toxicity*
  • Spermatogenesis / drug effects
  • Spermatogonia / drug effects

Substances

  • Androgen Antagonists
  • Oxazoles
  • Linuron
  • Cyproterone Acetate
  • Dichlorodiphenyl Dichloroethylene
  • vinclozolin