Record Display for the EPA National Library Catalog

RECORD NUMBER: 7 OF 7

OLS Field Name OLS Field Data
Main Title Steroidogenic Assessment Using Ovary Culture in Cycling Rats: Effects of Bis(2-Diethylhexyl) Phthalate on Ovarian Steroid Production.
Author Laskey, J. W. ; Berman, E. ;
CORP Author Health Effects Research Lab., Research Triangle Park, NC. Reproductive Toxicology Branch.
Publisher c1993
Year Published 1993
Report Number EPA/600/J-93/113;
Stock Number PB93-181022
Additional Subjects Ovary ; Steroids ; Estrus ; Toxicology ; Biosynthesis ; Rats ; In vitro analysis ; Chorionic gonadotropins ; In vivo analysis ; Reprints ; Phthalic acid/bis(2-diethylhexyl)
Holdings
Library Call Number Additional Info Location Last
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Status
NTIS  PB93-181022 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. NTIS 08/23/1993
Collation 11p
Abstract
In vitro whole-ovary culture in rats was used to characterize ovarian steroidogenesis and to evaluate changes produced by in vivo exposure to bis(2-diethylhexyl) phthalate (DEHP). Steroidogenic profiles (progesterone (P4), estradiol (E2), and testosterone (T)) from minced ovary cultures were obtained in untreated immature and mature rats, and from mature rats treated with DEHP. A one-hour incubation without human chorionic gonadotropin (hCG) was used to produce a basal steroidogenic profile. Three one-hour incubations with hCG were used to produce a stimulated profile. Using a multivariate statistical analysis, a combination of basal and stimulated ovarian steroid profiles correctly identified the stage of the cycle all untreated rats. Alone, basal or stimulated ovarian steroid profiles correctly identified the stage of the cycle in more than 90% of the rats. The statistical analysis using a combination of variables (multivariate) indicated that DEHP treated rats were significantly different (P < 0.001) from sham treated rats. In fact, the alteration caused by DEHP in the in vitro ovarian steroidogenic profile was most apparent in rats on vaginal diestrus and estrus. In DEHP-treated rats in diestrus, ovarian steroidogenesis appeared to shift to the production of more T and E2 than in untreated rats in diestrus.