| Literature DB >> 21530639 |
Melanie J P Fraites1, Michael G Narotsky, Deborah S Best, Tammy E Stoker, Lori K Davis, Jerome M Goldman, Michelle G Hotchkiss, Gary R Klinefelter, Alaa Kamel, Yaorong Qian, Lynda Podhorniak, Ralph L Cooper.
Abstract
Few studies have investigated the long-term effects of atrazine (ATR) following in utero exposure. We evaluated the effects of gestational exposure of Sprague Dawley dams to ATR (0, 1, 5, 20, or 100mg/kg-d) on the reproductive development of male offspring. We also quantified the distribution of ATR and its chlorinated metabolites in maternal, fetal, and neonatal fluid and tissue samples following gestational and/or lactational exposure. Dose-dependent levels of chlorotriazines, primarily diamino-s-chlorotriazine, were present in most samples analyzed, including fetal tissue. In utero exposure to 1-20mg/kg-d ATR did not alter testosterone production, the timing of puberty, play behavior, or other androgen-dependent endpoints of male offspring. Significant maternal toxicity and postnatal mortality were observed at 100mg/kg-d. We conclude that, although levels of chlorotriazines within the fetus were considerable, gestational exposures of 1-20mg/kg-d do not lead to alterations in the measures of male development examined in this study. Published by Elsevier Inc.Entities:
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Year: 2011 PMID: 21530639 DOI: 10.1016/j.reprotox.2011.04.003
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143