Characterization of the period of sensitivity of fetal male sexual development to vinclozolin

Citation
Cj. Wolf et al., Characterization of the period of sensitivity of fetal male sexual development to vinclozolin, TOXICOL SCI, 55(1), 2000, pp. 152-161
Citations number
59
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGICAL SCIENCES
ISSN journal
10966080 → ACNP
Volume
55
Issue
1
Year of publication
2000
Pages
152 - 161
Database
ISI
SICI code
1096-6080(200005)55:1<152:COTPOS>2.0.ZU;2-D
Abstract
Vinclozolin is a fungicide whose metabolites are androgen receptor (AR) ant agonists. Previous work in our laboratory showed that perinatal administrat ion of vinclozolin to rats results in malformations of the external genital ia, permanent nipples, reduced anogenital distance (AGD), and reduced semin al vesicle, ventral prostate, and epididymal weights. The objectives of thi s study were to determine the most sensitive period of fetal development to antiandrogenic effects of vinclozolin and to identify a dosing regime that would induce malformations in all of the male offspring. Pregnant rats wer e dosed with 400 mg vinclozolin/kg/day on either GD 12-13, GD 14-15, GD 16- 17, GD 18-19, or GD 20-21, or with corn oil (2.5 ml/kg) from GD 12 through GD 21 (Experiment 1). All 2-day periods in which significant effects were p roduced were included in an extended dosing period, GD 14 through GD 19, in which pregnant rats were dosed with 200 or 400 mg vinclozolin/kg (Experime nt 2). In Experiment 1, significant effects of vinclozolin were observed in rats dosed on gestation days (GD) 14-15, GD 16-17, and GD 18-19, while the most significant effects were observed in rats treated on GD 16-17. These effects include reduced AGD; presence of areolas, nipples, and malformation s of the phallus; and reduced levator ani/bulbocavernosus weight. In contra st, ventral prostate weight was reduced only in the GD 18-19 group. The exp anded dosing regime (Experiment 2) increased the percentage of male offspri ng with genital malformations (> 92%), and retained nipples (100%), further reduced the weight of the ventral prostate, and reduced the weight of the seminal vesicles. In addition, malformations were more severe and included vaginal pouch and ectopic/undescended testes. The latter was induced only i n the 400 mg/kg group. These data indicate that the reproductive system of the fetal male rat is most sensitive to antiandrogenic effects of vinclozol in on GD 16 and 17, although effects are more severe and 100% of male offsp ring are affected with administration of vinclozolin from GD 14 through GD 19.