期刊文献+

白藜芦醇对去卵巢大鼠骨质疏松症的保护作用 被引量:7

Protective effects and mechanisms of resveratrol on the rats suffering with osteoporosis
原文传递
导出
摘要 目的探讨白藜芦醇(RES)对去卵巢大鼠骨质疏松动物模型的保护作用及其分子机制。方法72只清洁级SD大鼠,按随机对照分组原则分为正常对照组、骨质疏松模型组、雌激素治疗组、RES低、中、高剂量治疗组,每组12只。除正常对照组外,双侧卵巢摘除术后1周,给予雌激素、RES治疗。12周后检测相关血清生化指标,光镜下观察骨组织形态学变化,双能X线吸收法测定其骨密度,RT-PCR检测骨组织中抗氧化酶(gpx1、trx1和γ-gt)mRNA的表达情况。结果血生化指标显示,骨质疏松模型组除血清雌激素水平明显低于其他各组外,其余指标均显著升高;骨组织形态学观察和骨密度检测提示,骨质疏松模型组骨组织呈现典型骨质疏松改变,骨组织中抗氧化酶表达降低;而雌激素治疗组和不同剂量RES治疗组血生化指标、骨组织形态学、骨密度和骨组织中抗氧化酶表达与正常对照组差异不明显。结论 RES具有类似于雌激素的维持骨形成和骨吸收平衡,拮抗骨质疏松症发生的作用,该作用与骨组织中抗氧化酶的表达量及活性相关。 Objective To investigate the protective effect and its mechanism of resveratrol (RES) on rats with osteoporosis. Methods A total of 72 clean grade female SD rats were randomly divided into six cohorts: control cohort, osteoporosis model cohort, estrogen pretreated cohort, low, median and high dosage RES pretreated cohorts. Except for rats in the control cohort, rats in other cohorts were treated by bilateral oophorectomy and pretreated with 17β-E2 and different dosage of resveratrol respectively, ranging from 1 to 12 weeks after operation. The blood parameters associating with osteoporosis were tested. Morphological observation of bone tissue was performed by HE staining under a microscope. Bone mineral density was measured by a dual-energy X-ray absorptiometry. The mRNA expression level of antioxidant enzymes (gpxl , trxl and γ-gt) were assayed by RT-PCR. Results Serum calcium, serum phosphate, ALP and TRAP increased obviously, but estrogen and calcium level in serum decreased sharply in the animal model. The bone tissue of the model manifested typical osteoporosis characteristics, and the expression of antioxidant enzymes was at a low level. After treated with estrogen or different dosages of resveratrol, the parameters and phenotypes mentioned above were almost close to the control cohort. Conclusion Resveratrol, likely estrogen, can maintain a balance of bone formation and absorbance, which is critical to the homeostasis of bone, antagonizing the osteoporosis pathology progression. This protective mechanism is associated with the expression and activity of antioxidant enzymes in bone tissue.
出处 《解剖学报》 CAS CSCD 北大核心 2012年第5期679-684,共6页 Acta Anatomica Sinica
基金 云南省应用基础研究重点基金资助项目(2008CC007) 云南省中青年学术和技术带头人后备人才培养基金资助项目(2009CI033)
关键词 骨质疏松 去势 白藜芦醇 雌激素 反转录一聚合酶链反应 大鼠 Osteoporosis Castration Resveratrol Estrogen RT-PCR Rat
  • 相关文献

参考文献15

  • 1Das DK, Mukherjee S, Ray D. Erratum to: resveratrol and red wine, healthy heart and longevity [J]. Heart Fail Rev, 2011, 16 (4) : 425-435.
  • 2CalabRESe G. Nonalcoholic compounds of wine: the phytoestrogen resveratrol and moderate red wine consumption during menopause [J]. Drugs Exp Clin RES, 1999, 25(2-3): 111-114.
  • 3Bottner M, Christoffel J, Rimoldi G, et al. Effects of long-term treatment with resveratrol and subcutaneous and oral estradiol administration on the pituitary-thyroid-axis [ J ]. Exp Clin Endocrinol Diabetes, 2006, 114 (2) : 82-90.
  • 4Ray PS, Maulik G, CordiS GA, et al. The red wine antioxidant resveratrol protects isolated rat hearts from ischemia reperfusion injury[ J]. Free Radic Biol Med, 1999, 27 (1) : 160-169.
  • 5Rayalam S, Della-Fera MA, Baile CA. Synergism between resveratrol and other phytochemicals: implications for obesity and osteoporosis [ J ]. Mol Nutr Food RES, 2011,55 ( 8 ) : 1177-1185.
  • 6Kalu DN. The ovariectomized rat model of postmenopausal bone loss [J]. Bone Miner, 1991, 15(3): 175-191.
  • 7Purdie DW. Consequences of long-tern hormone replacement therapy [J]. Br Med Bull, 2000, 56(3) : 809-823.
  • 8Saleh NK, Saleh HA. Olive Oil effectively mitigates ovariectomy- induced osteoporosis in rats [ J]. BMC Complement Ahern Med, 2011, 11: 10.
  • 9Bhavnani BR. Estrogens and menopause: pharmacology of conjugated equine estrogens and their potential role in the prevention of neurodegenerative diseases such as Alzheimer' s [ J ]. J Steroid Biochem Mol Biol, 2003, 85(2-5) : 473-482.
  • 10Lane NF, Yao W. Developments in the scientific understanding of osteoporosis [ J]. Arthritis Res Ther, 2009, 11 (3) : 228.

同被引文献44

  • 1原发性骨质疏松症诊疗指南(讨论稿)[J].中华全科医师杂志,2006,5(8):455-457. 被引量:65
  • 2MIZUTANI K, IKEDA K, KAWAI Y, et al. Resveratrol stimu- lates the proliferation and differentiation of osteoblastic MC3T3 - E1 cells[J]. Biochem Biophys Res Commun, 1998, 253 (3): 859 - 863.
  • 3MIZUTANI K, IKEDA K, KAWAI Y, et al. Resveratrol attenu- ates ovariectomy -induced hypertension and bone loss in stroke - prone spontaneously hypertensive rats [ J ]. J Nutr Sci Vitaminol (Tokyo) , 2000, 46(2) : 78 -83.
  • 4SONG L H, PAN W, YU Y H, et al. Resveratrol prevents CsA in- hibition of proliferation and osteoblastic differentiation of mouse bone marrow - derived mesenchymal stem cells through an ER/NO/ cGMP pathway[J]. Toxicol In Vitro, 2006, 20(6) : 915 -922.
  • 5BACKESJO C M, LI Y, LINDGREN U, et al. Activation of Sirtl decreases adipocyte formation during osteoblast differentiation of mesenchymal stem ceils[ J]. J Bone Miner Res, 2006, 21 (7) : 993 - 1002.
  • 6PICARD F, KURTEV M, CHUNG N, et al. Sirtl promotes fat mobilization in white adipocytes by repressing PPAR - gamma [ J ]. Nature, 2004, 429 (6993) : 771 - 776.
  • 7DAI Z, LI Y, QUARLES L D, et al. Resveratrol enhances prolife- ration and osteoblastic differentiation in human mesenchymal stem cells via ER -dependent ERK1/2 activation[J]. Phytomedicine, 2007, 14(12) : 806 -814.
  • 8边艳峰,杨晓明,冯杰,张辉,周强,张馨中.颅脑外伤大鼠急性期血清硫化氢浓度的变化及其意义[J].中国药物与临床,2010,10(10):1112-1113. 被引量:6
  • 9原发性骨质疏松症诊治指南(2011年)[J].中华骨质疏松和骨矿盐疾病杂志,2011,4(1):2-17. 被引量:1842
  • 10王彤,庞莉,黄晖,王文艳.远针近推疗法对老年性骨质疏松症骨代谢生化指标的影响[J].中国针灸,2012,32(1):13-16. 被引量:16

引证文献7

二级引证文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部