Literature DB >> 2925022

A dose-response analysis of methoxychlor-induced alterations of reproductive development and function in the rat.

L E Gray1, J Ostby, J Ferrell, G Rehnberg, R Linder, R Cooper, J Goldman, V Slott, J Laskey.   

Abstract

In the present study rats were dosed from weaning, through puberty and gestation, to Day 15 of lactation with methoxychlor at 25, 50, 100, or 200 mg/kg/day. Morphological landmarks of puberty were measured, including the ages at vaginal opening, first estrus, and first estrous cycle in females and at preputial separation in males. In the female, estrous cyclicity, fertility, litter size, number of implantation sites, organ weights, and ovarian and uterine histology were also measured. The viability of the offspring (F1) and their fertility were evaluated using a continuous breeding protocol. Males were necropsied after breeding, the reproductive organs were weighed, and the cauda epididymal sperm counts were determined. One testis was used for histopathology, while the other was used to quantify interstitial fluid (IF) content, IF testosterone concentration, and testicular sperm production. Testosterone and androgen-binding protein were measured in the caput epididymis, and sperm motility and morphology were evaluated from a caudal sample. The serum and pituitary were saved for hormonal determinations. Methoxychlor accelerated the age at vaginal opening and first estrus, and the vaginal smears were cornified. Growth was retarded at 100 and 200 mg/kg/day and fertility was reduced when the females were bred with untreated or similarly treated males. In the highest-dose group, the mated females went from constant estrus into pseudopregnancy following mating, but they had no implants. In males, methoxychlor treatment markedly reduced growth, seminal vesicle weight, cauda epididymal weight, caudal sperm content, and pituitary weight. Puberty was delayed in the two highest-dosage groups. Testicular sperm measures were much less affected than caudal measures. Testis weight and histology were slightly affected, and testicular sperm production, sperm morphology, and motility were unaffected. Endocrine function of the testes and pituitary was altered by methoxychlor administration. Leydig cell testosterone production, in response to human chorionic gonadotropin challenge, was reduced and pituitary levels of prolactin, thyroid-stimulating hormone (TSH), and follicle-stimulating hormone (FSH) were altered. In contrast, serum levels of prolactin, FSH, and luteinizing hormone were unaffected. Serum TSH was reduced by 50% of control at 100 and 200 mg/kg/day, while pituitary levels were increased. Gonadotropin-releasing hormone concentration in the mediobasal hypothalamus was also elevated. In spite of the many reproductive alterations, the fertility of treated males was not reduced when they were mated with untreated females.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2925022     DOI: 10.1016/0272-0590(89)90065-1

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  42 in total

Review 1.  Disruption of androgen receptor signaling in males by environmental chemicals.

Authors:  Doug C Luccio-Camelo; Gail S Prins
Journal:  J Steroid Biochem Mol Biol       Date:  2011-04-13       Impact factor: 4.292

Review 2.  Epigenetic effects of endocrine-disrupting chemicals on female reproduction: an ovarian perspective.

Authors:  Aparna Mahakali Zama; Mehmet Uzumcu
Journal:  Front Neuroendocrinol       Date:  2010-07-04       Impact factor: 8.606

Review 3.  Developmental exposure to environmental endocrine disruptors: consequences within the ovary and on female reproductive function.

Authors:  Mehmet Uzumcu; Rob Zachow
Journal:  Reprod Toxicol       Date:  2006-11-06       Impact factor: 3.143

4.  Early life exposure to endocrine-disrupting chemicals causes lifelong molecular reprogramming of the hypothalamus and premature reproductive aging.

Authors:  Andrea C Gore; Deena M Walker; Aparna M Zama; AnnMarie E Armenti; Mehmet Uzumcu
Journal:  Mol Endocrinol       Date:  2011-10-20

5.  Identification of previously unrecognized antiestrogenic chemicals using a novel virtual screening approach.

Authors:  Ching Y Wang; Ni Ai; Sonia Arora; Eric Erenrich; Karthigeyan Nagarajan; Randy Zauhar; Douglas Young; William J Welsh
Journal:  Chem Res Toxicol       Date:  2006-12       Impact factor: 3.739

6.  Effects of pesticides used in agriculture on the development of precocious puberty.

Authors:  Samim Ozen; Sukran Darcan; Petek Bayindir; Ercument Karasulu; Damla Goksen Simsek; Tahir Gurler
Journal:  Environ Monit Assess       Date:  2011-07-30       Impact factor: 2.513

7.  Rebuttal of "Flawed Experimental Design Reveals the Need for Guidelines Requiring Appropriate Positive Controls in Endocrine Disruption Research" by (Vom Saal 2010).

Authors:  Leon Earl Gray; Bryce Ryan; Andrew K Hotchkiss; Kevin M Crofton
Journal:  Toxicol Sci       Date:  2010-03-05       Impact factor: 4.849

8.  In utero exposure to simvastatin reduces postnatal survival and permanently alters reproductive tract development in the Crl:CD(SD) male rat.

Authors:  Brandiese E J Beverly; Johnathan R Furr; Christy S Lambright; Vickie S Wilson; Barry S McIntyre; Paul M D Foster; Greg Travlos; L Earl Gray
Journal:  Toxicol Appl Pharmacol       Date:  2019-01-11       Impact factor: 4.219

9.  Windows of sensitivity to toxic chemicals in the development of reproductive effects: an analysis of ATSDR's toxicological profile database.

Authors:  Melanie C Buser; Henry G Abadin; John L Irwin; Hana R Pohl
Journal:  Int J Environ Health Res       Date:  2018-07-19       Impact factor: 3.411

Review 10.  Fifteen years after "Wingspread"--environmental endocrine disrupters and human and wildlife health: where we are today and where we need to go.

Authors:  Andrew K Hotchkiss; Cynthia V Rider; Chad R Blystone; Vickie S Wilson; Phillip C Hartig; Gerald T Ankley; Paul M Foster; Clark L Gray; L Earl Gray
Journal:  Toxicol Sci       Date:  2008-02-16       Impact factor: 4.849

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.