Literature DB >> 1764629

A comparative study of the actions of tamoxifen, estrogen and progesterone in the ovariectomized rat.

D N Kalu1, E Salerno, C C Liu, R Echon, M Ray, M Garza-Zapata, B W Hollis.   

Abstract

This study was undertaken to examine the separate and combined effects of tamoxifen (T), estrogen (E2) and progesterone (P) treatment on ovariectomized (Ooph) rats. The animals were treated for 40 days. Ovariectomy reduced cancellous bone volume at the proximal tibia by 50%. Estradiol treatment completely prevented the bone loss and further increased bone volume 77% over the level for the control group. Tamoxifen also prevented the ovariectomy induced bone loss, but significantly reduced the increase in cancellous bone induced by estradiol. In the ovariectomized rats, cancellous bone apposition rate increased 23%. This increase was suppressed 63% by estradiol, and only 18% by tamoxifen. Tamoxifen significantly suppressed the inhibitory effect of estradiol on cancellous bone apposition rate. In contrast, the effect of progesterone treatment was only marginal. Our findings indicate that the action of tamoxifen on bone is influenced by the ambient level of circulating estradiol, such that in estrogen deficiency, tamoxifen has a weak estrogen agonist action on bone, and in the presence of estrogen it has anti-estrogen actions, with the dose level and mode of administration employed. These conclusions have implications for the use of tamoxifen in the treatment of pre- and postmenopausal women.

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Year:  1991        PMID: 1764629     DOI: 10.1016/0169-6009(91)90002-h

Source DB:  PubMed          Journal:  Bone Miner        ISSN: 0169-6009


  10 in total

1.  Ovarian status influences the skeletal effects of tamoxifen in adult rats.

Authors:  J D Sibonga; G L Evans; E R Hauck; N H Bell; R T Turner
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

2.  Age and gender specific stimulation of creatine kinase specific activity by gonadal steroids in human bone-derived cells in culture.

Authors:  S Katzburg; A Ornoy; D Hendel; M Lieberherr; A M Kaye; D Somjen
Journal:  J Endocrinol Invest       Date:  2001-03       Impact factor: 4.256

Review 3.  Calmodulin-an often-ignored signal in osteoclasts.

Authors:  John P Williams; Keith Micoli; Jay M McDonald
Journal:  Ann N Y Acad Sci       Date:  2010-03       Impact factor: 5.691

4.  Elemental composition of bone minerals in women with breast cancer treated with adjuvant tamoxifen.

Authors:  J A Kalef-Ezra; N Pavlidis; G Klouvas; A Karantanas; I Hatzikonstantinou; D Glaros
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

5.  Inhibition of the progesterone nuclear receptor during the bone linear growth phase increases peak bone mass in female mice.

Authors:  Wei Yao; Weiwei Dai; Mohammad Shahnazari; Aaron Pham; Zhiqiang Chen; Haiyan Chen; Min Guan; Nancy E Lane
Journal:  PLoS One       Date:  2010-07-01       Impact factor: 3.240

6.  Bone growth and turnover in progesterone receptor knockout mice.

Authors:  David J Rickard; Urszula T Iwaniec; Glenda Evans; Theresa E Hefferan; Jamie C Hunter; Katrina M Waters; John P Lydon; Bert W O'Malley; Sundeep Khosla; Thomas C Spelsberg; Russell T Turner
Journal:  Endocrinology       Date:  2008-02-14       Impact factor: 4.736

7.  Hormone replacement therapy increases serum 1,25-dihydroxyvitamin D: A 2-year prospective study.

Authors:  H J van Hoof; M J van der Mooren; L M Swinkels; R Rolland; T J Benraad
Journal:  Calcif Tissue Int       Date:  1994-12       Impact factor: 4.333

8.  Growth hormone normalizes vertebral strength in ovariectomized rats.

Authors:  C Eschen; T T Andreassen
Journal:  Calcif Tissue Int       Date:  1995-11       Impact factor: 4.333

9.  Loss of cancellous bone mass and connectivity in ovariectomized rats can be restored by combined treatment with parathyroid hormone and estradiol.

Authors:  V Shen; D W Dempster; R Birchman; R Xu; R Lindsay
Journal:  J Clin Invest       Date:  1993-06       Impact factor: 14.808

10.  Preventive role of estradiol on kidney injury induced by renal ischemia-reperfusion in male and female rats.

Authors:  Akram Iran-Nejad; Mehdi Nematbakhsh; Fatemeh Eshraghi-Jazi; Ardeshir Talebi
Journal:  Int J Prev Med       Date:  2015-03-20
  10 in total

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