Methoxychlor stimulates estrogen-responsive messenger ribonucleic acids inmouse uterus through a non-estrogen receptor (Non-ER)alpha and Non-ER betamechanism

Citation
D. Ghosh et al., Methoxychlor stimulates estrogen-responsive messenger ribonucleic acids inmouse uterus through a non-estrogen receptor (Non-ER)alpha and Non-ER betamechanism, ENDOCRINOL, 140(8), 1999, pp. 3526-3533
Citations number
51
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
ENDOCRINOLOGY
ISSN journal
00137227 → ACNP
Volume
140
Issue
8
Year of publication
1999
Pages
3526 - 3533
Database
ISI
SICI code
0013-7227(199908)140:8<3526:MSEMRA>2.0.ZU;2-Y
Abstract
This study examined the effects of the xenoestrogen methoxychlor (Mxc) on m essenger RNA (mRNA) concentrations of two estrogen-responsive uterine genes , lactoferrin (LF) and glucose-6-phosphate dehydrogenase (G6PD). Ovariectom ized wild-type (WT) and estrogen receptor (ER) alpha-knockout (ER alpha KO) mice were treated with Mxc or estradiol-17 beta (E-2) to determine whether Mxc acts via pathways that involve ER alpha. In WT mice, both E-2 and Mxc stimulated increases in uterine LF and GGPD mRNA concentrations in a dose-d ependent manner. Competitive pretreatment with the pure antiestrogen ICI 18 2,780 dramatically reduced E-2-stimulated increases in mRNA concentrations but had no effect on Mxc-induced effects. Competitive pretreatment with E-2 had only a partially inhibitory effect on Mxc-induced responses. In the ER alpha KO mouse, E-2 had little effect on uterine LF or G6PD mRNA concentra tions, whereas Mxc stimulated marked increases in both LF and G6PD mRNAs. T he Mxc-induced increases in LF and G6PD mRNAs in the ER alpha KO mouse were not suppressed by competitive pretreatment with either E-2 or ICI 182,780. Fold increases in mRNA concentrations for both genes induced by Mxc were s imilar for WT and ER alpha KO mice. The results surprisingly indicate that a xenoestrogen, Mxc, can increase LF and G6PD mRNA concentrations by a mech anism that is not mediated through ER alpha or ER beta, and acts through an other pathway.