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The Effect of Estrogen on the Restoration of Bone Mass and Bone Quality in Ovariectomized Rats 被引量:3

The Effect of Estrogen on the Restoration of Bone Mass and Bone Quality in Ovariectomized Rats
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摘要 To evaluate the effect of estrogen on its ability to restore the bone mass and bone quality in ovariectomized rats by examining the changes of bone morphology and histomorphometry, 3- month-old rats were divided randomly into 4 groups: normal control, ovariectomized (OVX), sham- operated (Sham-O) and OVX plus estrogen (OVX+E2). Treatment initiated from the day 8 weeks after operation and continued for 12 weeks. Bone morphology and histomorphometry were examined afterwards. Results showed that comparing to control group, the trabecular bone in OVX appeared thinner and reduced in the amount. The connectivity between trabecula was decreased and the struc- ture disordered. The free-end of trabecula was increased. The cavity of bone marrow enlarged. After treatment with estrogen, above changes improved remarkably by different degree, although did not reach the normal face. The bone histomorphometry results damonstrated that estrogen treatment in- creased bone mass and the amount of trabecula by 129% and 132% respectively (P<0. 05). The activity of bone resorption decreased significantly and the rate of bone formation increased to 203%. These results suggest that treatment of ovariectomized rats with estrogen can not only increase bone mass, also improve the bone structure and enhance the property of bone mechanics. To evaluate the effect of estrogen on its ability to restore the bone mass and bone quality in ovariectomized rats by examining the changes of bone morphology and histomorphometry, 3- month-old rats were divided randomly into 4 groups: normal control, ovariectomized (OVX), sham- operated (Sham-O) and OVX plus estrogen (OVX+E2). Treatment initiated from the day 8 weeks after operation and continued for 12 weeks. Bone morphology and histomorphometry were examined afterwards. Results showed that comparing to control group, the trabecular bone in OVX appeared thinner and reduced in the amount. The connectivity between trabecula was decreased and the struc- ture disordered. The free-end of trabecula was increased. The cavity of bone marrow enlarged. After treatment with estrogen, above changes improved remarkably by different degree, although did not reach the normal face. The bone histomorphometry results damonstrated that estrogen treatment in- creased bone mass and the amount of trabecula by 129% and 132% respectively (P<0. 05). The activity of bone resorption decreased significantly and the rate of bone formation increased to 203%. These results suggest that treatment of ovariectomized rats with estrogen can not only increase bone mass, also improve the bone structure and enhance the property of bone mechanics.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2000年第4期283-286,共4页 华中科技大学学报(医学英德文版)
基金 This project was supported by a grant from the NationalNatural Science Foundation of China (No. 39770930).
关键词 ESTROGEN ovariectomized rats MORPHOLOGY HISTOMORPHOMETRY OSTEOPOROSIS estrogen ovariectomized rats morphology histomorphometry osteoporosis
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参考文献6

  • 1Harold M. Frost.On rho, a marrow mediator, and estrogen: Their roles in bone strength and "mass" in human females, osteopenias, and osteoporoses—insights from a new paradigm[J].Journal of Bone and Mineral Metabolism.1998(2)
  • 2Stavros C M,Robert L J.Bone marrow, cytokines, andbone remodeling[].The New England Journal of Medicine.1995
  • 3Parfitt A M.Trabecular bone architecture in the patho-genesis and prevention of fracture[].The American Journal of Medicine.1987
  • 4Miyaura C,Kusano K,Masuzawa T et al.Endogenousbone-resorbing factors in estrogen deficiency: cooperativeeffects of IL-i and IL-6[].Journal of Bone and Mineral Research.1995
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  • 6Kitazawa R,Kimble R B,Vannice J L et al.Interleukin--I receptor antagonist and tumor necrosis factor bindingprotein decrease osteoclast formation and bone resorptionin ovariectomized mice[].The Journal of Clinical Investigation.1994

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