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阿伐他汀对去势大鼠骨折愈合的影响

Study on Atorvastatin' s effects on fracture union of emasculated rats
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摘要 目的研究阿伐他汀局部注射对去势大鼠骨折愈合的影响。方法2月龄雌性SD大鼠采用去势方法模拟人绝经后骨质疏松症,进一步建立胫骨骨折髓内钉内固定模型,实验组于骨折端皮下注射阿伐他汀(10mg.kg-1.d-1×5d),对照组注射无阿伐他汀的溶剂。骨折后1、2、4周取标本,通过X线片、生物力学、组织病理学以及组织形态计量学等评价两组骨折愈合质量。结果与对照组相比,实验组骨痂横截面积在骨折后1周、2周分别增加24.3%(p<0.05)和33.2%(p<0.05);骨痂最大载荷在骨折后2周、4周分别增加43.1%(p<0.05)和69.8%(p<0.05);组织学显示实验组新生编织骨较对照组多且排列致密。结论局部应用阿伐他汀可促进去势大鼠骨折愈合。 Objective To explore the influence of Atorvastatin on fracture union of emasculated rats. Methods Postmenopausal osteoporosis was simulated on emasculated female rats of 2 months old , further model of internal fixation with bone nail in treating tibia fracture was developed . In treating group , Atorvastatin was subcutaneous injected (10mg·kg^-1·day^-1×5day) locally at fracture site , in control group , solution without Atorvastatin was used as control .Spacemen were collected 1,2,4 weeks after fracture , the quality of fracture union was evaluated by X-ray ,vitedynamics,histopathology and morphometry. Results The section area of osteotylus in the treating group inereased 24.3% (p〈0.05) and33.2% (p〈0.05) in one and two weeks after fracture; maximal load of osteotylus increased 43.1% (p〈0.05) and 69.8 % (p〈0.05) two and four weeks after fracture ; histological finding showed neogenesis woven bones were more and compactly arranged in treating group than those in control one . Conclusions Local Atorvastatin injection helps the fracture union in fracture union of emasculated rats.
作者 王慧 王大风
出处 《浙江临床医学》 2008年第5期582-584,共3页 Zhejiang Clinical Medical Journal
关键词 阿伐他汀 大鼠 骨质疏松 骨折愈合 Atorvastatin Rat Osteoporosis fracture union
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  • 1Mundy G, Garrett R, Harris S, et al. Stimulation of bone formation in vitro and in rodents by statins. Science, 1999, 286(5446) : 1946 - 1949.
  • 2Ohno T, Shigetomi M, lhara K, et al. Skeletal reconstruction by vascularized allogenic bone transplantation: effects of stafin in rats. Transplantation, 2003,76(5) : 869 - 871.
  • 3Blum CB. Comparison of properties of four inhibitors of 3 - hdroxy - 3methyglutary -coenzyme A reductase. Am J Cardiol, 1994, 73(14) :3D - 11D.
  • 4Montagnani A, Gonnelli S, Cepollaro C, et al. Effect of simvastatin treatment on bone mineral density and bone turnover in hypercholesterolemic postmenopausal women: a 1 - year longitudinal study. Bone, 2003,32(4):427-433.
  • 5Schoofs MW, Sturkenboom MC, Klift M, et al. HMG - CoA reductase inhibitors and the risk of vertebral fracture. J Bone Miner Res, 2004, 19 (9) : 1525 - 1530.
  • 6Tikiz C, Tikiz H, Taneli F, et al. Effects of simvastalin on bone mineral density and remodeling parameters in postmenopausal osteopenic subjects: 1 - year follow-up study. Clin Rheumatol, 2005,24(5): 447 -452.
  • 7Rejnmark L, Buus NH, Vestergaard P, et al. Effects of simvastatin on bone turnover and BMD: a 1 - year randomized controlled trial in postmenopansal osteopenic women. J Bone Miner Res, 2004, 19(5):737 - 744.
  • 8Maritz FJ, Conradie MM, Hulley PA, et al, Effect of statins on bone mineral density and bone histomorphometry in rodents, Arterioscler Thromb Vasc Biol, 2001,21(10):1636- 1641.
  • 9Gerson R J, MacDonald JS, Alberts AW, et al. Animal safety and toxicology of simvastatin and related hydroxy - methylglutaryl - coenzyme A reductase inhibitors. Am J Med, 1989,87(4A) :28S- 38S.
  • 10Skoghmd B, Forshmd C, Aspenberg P. Simvastatin improves fracture healing in mice. J Bone Miner Res, 2002,17 (11 ):2004- 2008.

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