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Selective estrogen receptor modulators and the vitamin D analogue eldecalcitol block bone loss in male osteoporosis.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2017 Jan 22; Vol. 482 (4), pp. 1430-1436. Date of Electronic Publication: 2016 Dec 11. - Publication Year :
- 2017
-
Abstract
- Rapid increases in the number of elderly people have dramatically increased the number of female and male osteoporosis patients. Osteoporosis often causes bone fragility fractures, and males exhibit particularly poor prognosis after these fractures, indicating that control of osteoporosis is crucial to maintain quality of men's lives. However, osteoporosis therapies available for men have lagged behind advances available for women. Here, we show that three selective estrogen receptor modulators (SERMs), namely, raloxifene, bazedoxifene, and tamoxifen, plus the vitamin D analogue ED71, also called eldecalcitol, completely block orchiectomy-induced, testosterone-depleted bone loss in male mice in vivo. Patients treated with hormone deprivation therapy for prostate cancer also exhibit male osteoporosis, and bone management is critical for these patients. Given that androgen replacement therapy is not an option for these patients, our results represent a novel approach potentially useful to control male osteoporosis.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Bone Density
Bone Density Conservation Agents pharmacology
Bone Diseases, Metabolic chemically induced
Bone Diseases, Metabolic prevention & control
Bone Resorption chemically induced
Bone and Bones drug effects
Indoles pharmacology
Male
Mice
Mice, Inbred C57BL
Orchiectomy
Raloxifene Hydrochloride pharmacology
Tamoxifen pharmacology
Testosterone deficiency
Vitamin D pharmacology
Bone Resorption prevention & control
Osteoporosis drug therapy
Selective Estrogen Receptor Modulators pharmacology
Vitamin D analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 482
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 27974229
- Full Text :
- https://doi.org/10.1016/j.bbrc.2016.12.053