Effects of Estrogen, Progesterone, and Methoxychlor on Surgically Induced Endometriosis in Rats
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This study investigated the effects of estrogen, progesterone, and methoxychlor on surgically induced endometriosis in a rat model.
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Abstract
Endometriosis is a disease of women where endometrial tissue is found growing at ectopic sites. While evidence suggesting a role for the ovarian hormones in endometriosis exists, no complete studies of the roles of estrogen and progesterone have heretofore been performed. Also, if estrogen has a role in the growth and/or maintenance of endometriosis, it is likely that the proestrogenic pesticide, methoxychlor (MXC), might also have such an effect. Sixty rats underwent surgery on Day 0 to induce endometriosis. On Day 21, all rats were ovariectomized. During surgery, the diameters of all endometriotic implants (which were fully developed) were measured. Starting on Day 21, groups of rats were treated daily, for 3 weeks, with (a) vehicle (b) estrone, 1 micrograms/rat, E;(c) progesterone, 2 mg/rat, P; (d) E + P, 1 micrograms + 2 mg; (e) MXC, 250 mg/kg; or (f) MXC + P, 250 mg/kg + 2 mg/rat. On Day 42, all rats were killed, and the diameters of all endometriotic sites were measured. While no differences in diameter were found across groups prior to ovariectomy, ovariectomy plus treatment altered the growth of endometriosis tissue. Progesterone and vehicle treatments produced results that were identical: regression of endometriotic sites. Both estrogen and MXC treatments maintained endometriotic site size at a level greater than that in the vehicle-treated group. The combination of progesterone with either estrone or MXC did not alter the effect of either chemical. We conclude that while estrogen promotes the growth of endometriosis, progesterone either produces regression or fails to maintain the sites. MXC, at a relatively high dose, supports the development of endometriosis. Concurrent progesterone treatment does not modulate the effects of estrone or MXC. These results suggest that exposure of women to high doses of MXC may exacerbate the development of endometriosis or contribute to its recurrence.
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Cited by (18)
- Induction of Endometriosis in a Menstruating Mouse Model (Mus musculus): A Translational Animal Disease Model 2025
- Optimizing a Translational Mouse Model of Endometriosis 2023
- Food groups and nutrients consumption and risk of endometriosis: a systematic review and meta-analysis of observational studies 2022
- Associations between Exposure to Organochlorine Chemicals and Endometriosis: A Systematic Review of Experimental Studies and Integration of Epidemiological Evidence 2021
- Mouse Model of Surgically-induced Endometriosis by Auto-transplantation of Uterine Tissue 2012
- Pelvic pain in endometriosis: is success of therapy gone in cigarette smoke? 2011
- Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample 2007
- Quantitative Assessment of Human Endometriotic Tissue Maintenance and Regression in a Noninvasive Mouse Model of Endometriosis 2004
- Endometriosis Model Development in Swine 2003
- Environmental Contaminants and Dietary Factors in Endometriosis 2002
- Dioxins and endometriosis: a plausible hypothesis. 2002
- Pharmacologic, but Not Dietary, Genistein Supports Endometriosis in a Rat Model 2001
- Molecular Action of GnRH Analogues on Ectopic Endometrial Cells 1998
- Morphologic characteristics of endometriosis in the mouse model: application to toxicology 1997
- Morphologic characteristics of endometriosis in the mouse model: application to toxicology 1997
- Continuous Exposure to 2,3,7,8-Tetrachlorodibenzo- <i>P</i> -Dioxin Inhibits the Growth of Surgically Induced Endometriosis in the Ovariectomized Mouse Treated with high Dose Estradiol 1997
- Promotion of endometriosis in mice by polychlorinated dibenzo-p-dioxins, dibenzofurans, and biphenyls. 1997
- Stimulating effects of 4-chlorodiphenyl ether on surgically induced endometriosis in the mouse 1997
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