Literature DB >> 8048058

2,2',4,4',5,5'- and 3,3',4,4',5,5'-hexachlorobiphenyl alteration of uterine progesterone and estrogen receptors coincides with embryotoxicity in mink (Mustela vision).

K A Patnode1, L R Curtis.   

Abstract

Female mink (Mustela vison) are highly sensitive to organochlorine (OC)-induced reproductive impairment. However, mechanisms of this reproductive toxicity are unknown. We have investigated the possible role of steroid receptors in embryotoxicity and reduced neonate weights. Anestrous, juvenile female mink and pregnant adult mink were exposed to 3,3',4,4',5,5'-hexachlorobiphenyl (3HCB), a coplanar polychlorinated biphenyl (PCB), or 2,2',4,4',5,5'-hexachlorobiphenyl (2HCB), a noncoplanar PCB congener. Both congeners impaired 17 beta-estradiol-stimulated (24 hr after ip administration of 100 micrograms E2 beta ip) up-regulation of uterine nuclear estrogen receptors (ERn) in anestrous mink. Embryotoxicity and reduced embryo growth were first observed 14 days after exposure to 0.4 mg 3HCB/kg > 0.8 mg 3HCB/kg > 20 mg 2HCB/kg. In pregnant mink, all 3HCB treatments significantly increased progesterone receptor dissociation constants (PR Kd). ER concentration and PR total receptor number (Rt) were increased by 20 mg 2HCB/kg > 0.8 mg 3HCB/kg, but were unaffected by 0.4 mg 3HCB/kg. Serum E2 beta was below assay detection limits. Progesterone (P) concentrations were increased by 2HCB, decreased by 0.8 mg 3HCB/kg, and unchanged by 0.4 mg 3HCB/kg. Hepatic cytochrome P450 (P450) was induced 1.8-fold in anestrous and 2.2-fold in pregnant mink by 3HCB. Ethoxyresorufin-O-deethylase (EROD) was induced 13- and 4-fold in anestrous and pregnant mink, respectively. 2HCB exposure resulted in decreased P450 concentration in anestrous juveniles, but had no effect on P450 during gestation or EROD activity at any time. We propose that embryotoxicity and retarded embryo growth result from impairment of PR function and that differences in the efficacy of HCB treatments are a result of their dose-dependent, partial estrogenic actions which increase PR Rt via up-regulation of ER.

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Year:  1994        PMID: 8048058     DOI: 10.1006/taap.1994.1133

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  6 in total

1.  Expression of the insulin-like growth factor II gene in polychlorinated biphenyl exposed female mink (Mustela vison) and their fetuses.

Authors:  B M Bäcklin; A Gessbo; M Forsberg; A Shokrai; B Rozell; W Engström
Journal:  Mol Pathol       Date:  1998-02

2.  Environmental contaminants in male river otters from Oregon and Washington, USA, 1994-1999.

Authors:  Robert A Grove; Charles J Henny
Journal:  Environ Monit Assess       Date:  2007-12-06       Impact factor: 2.513

3.  Polychlorinated biphenyls and reproductive hormones in female polar bears at Svalbard.

Authors:  Marte Haave; Erik Ropstad; Andrew E Derocher; Elisabeth Lie; Ellen Dahl; Øystein Wiig; Janneche U Skaare; Bjørn Munro Jenssen
Journal:  Environ Health Perspect       Date:  2003-04       Impact factor: 9.031

Review 4.  Research needs for the risk assessment of health and environmental effects of endocrine disruptors: a report of the U.S. EPA-sponsored workshop.

Authors:  R J Kavlock; G P Daston; C DeRosa; P Fenner-Crisp; L E Gray; S Kaattari; G Lucier; M Luster; M J Mac; C Maczka; R Miller; J Moore; R Rolland; G Scott; D M Sheehan; T Sinks; H A Tilson
Journal:  Environ Health Perspect       Date:  1996-08       Impact factor: 9.031

Review 5.  Tinkering with the tinkerer: pollution versus evolution.

Authors:  G A Fox
Journal:  Environ Health Perspect       Date:  1995-05       Impact factor: 9.031

6.  Inhibition of gap junctional intercellular communication in normal human breast epithelial cells after treatment with pesticides, PCBs, and PBBs, alone or in mixtures.

Authors:  K S Kang; M R Wilson; T Hayashi; C C Chang; J E Trosko
Journal:  Environ Health Perspect       Date:  1996-02       Impact factor: 9.031

  6 in total

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