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Hormone replacement therapy in the menopause: a suitable animal model
The Journal of Endocrinology
|October 1, 1979
Summary
This study shows that ethynyl oestradiol and oestrone sulphate treatments in mice cause endometrial hyperplasia and affect bone remodelling. These findings suggest the CBA mouse is a good model for studying human menopause and hormone replacement therapy.
Area of Science:
- Endocrinology
- Reproductive Biology
- Gerontology
Background:
- The human climacteric involves hormonal changes and physiological effects.
- Hormone replacement therapy (HRT) is a common treatment for menopausal symptoms.
- Understanding animal models is crucial for studying human menopause and HRT.
Purpose of the Study:
- To investigate the effects of ethynyl oestradiol and oestrone sulphate on female CBA mice.
- To evaluate the suitability of the CBA mouse as a model for human climacteric studies and HRT response.
Main Methods:
- Cyclical oral administration of ethynyl oestradiol or oestrone sulphate to 11-month-old female CBA mice for 3 months.
- Ovarian atrophy assessment.
- Genital tract tissue analysis using electron microscopy.
- Measurement of uterine cytoplasmic oestrogen receptors.
- Monitoring of serum luteinizing hormone levels.
- Evaluation of cortical-endosteal bone remodelling.
Main Results:
- Ovarian atrophy observed in all treated mice.
- Genital tract tissues responded to both oestrogens, with increased cellular metabolic activity in endometrium and urothelium.
- Endometrial hyperplasia occurred, more pronounced with oestrone sulphate.
- Uterine cytoplasmic oestrogen receptors doubled.
- Serum luteinizing hormone levels decreased by 50%, indicating intact hypothalamic-pituitary function.
- Both oestrogens improved skeletal balance via bone remodelling.
Conclusions:
- Ethynyl oestradiol and oestrone sulphate induce significant physiological changes in female CBA mice.
- The CBA mouse model demonstrates responsiveness to oestrogens, mirroring aspects of the human climacteric.
- This mouse model is suitable for research into human menopause and hormone replacement therapy efficacy.