摘要
目的 研究国产依普拉封片(ipriflavone)防治绝经后骨质疏松症疗效的生化学监测及疗效机制。方法 绝经后骨质疏松症54例,其中治疗组30例服用国产依普拉封片合用钙尔奇-D治疗6个月,对照组24例单独服用钙尔奇-D6个月,检测两组用药前后骨代谢生化指标。结果 治疗组结果表明骨吸收的指标:甲状旁腺素(PTH)、抗酒石酸盐酸性磷酸酶(TRAP)、尿胶原交联/肌酐比值(Crosslaps/Cr)均明显降低;骨形成/骨转换的指标:碱性磷酸酶(ALP)、骨钙素(BGP)、I型前胶原羧基端前肽(PICP)亦下降;骨重建刺激因子:胰岛素样生长因子-1(IGF-1)显著升高。对照组,TRAP也有轻度下降。结论依普拉封片能明显的影响骨代谢:抑制骨吸收,降低骨转换, 减少骨量丢失,治疗1个月即可出现作用;刺激骨重建,增加骨密度,能够有效地防治绝经后骨质疏松症。生化指标可用于疗效的早期监测。
Abstract
OBJECTIVE To monitor the change of biochemistry in patients with postmenopausal osteoporosis after intaking ipriflavone and discuss its action mechanism. METHODS 54 patients with post-menopause osteoporosis were divided into 2 groups:30 patients were administrated with ipriflavone and Caltrate-D for 6 months.24 patients in control group were only given Caltrate-D for 6 months.The bone biochemical indexes were monitored before and after the treatment. RESULTS PTH, TRAP and Crosslaps/Cr, the indexes of bone absorption, decreased markedly; ALP, BGP and PICP, the indexes of bone formation/turnover, decreased markedly.IGF-1, strong stimulator of bone rebuild, significantly increased.In the control group,Ca2+in blood and TRAP lightly decreased. CONCLUSION The results indicated ipriflavone decreased the bone absorption and bone turnover rate, prevented bone loss.The efficacy appeared in 1st month after administration;stimulating bone rebuild,and raise BMD.It is effective in preventing and treating postmenopausal osteoporosis.Biochemistry index can be used to monitor the effect of treatment early.
关键词
依普拉封 /
骨质疏松 /
骨
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Key words
ipriflavone /
postmenopausal osteoporosis /
bone
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李书琴 潘莉莉 刘英敏 李强 郭兑山 潘作东 崔少千 聂晶.
国产依普拉封片防治绝经后骨质疏松症生化监测[J]. 中国药学杂志, 2000, 35(12): 849-851
LI Shu-qin;PN Li-li;LIU Ying-min;LI Qing;GUO Dui-shn;PN Zuo-dong;CUI Sho-qin;NIE Jing.
Biochemistry monitoring in patients with postmenopausal osteoporosis after ipriflavone intake[J]. Chinese Pharmaceutical Journal, 2000, 35(12): 849-851
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参考文献
[1]Benvenuti S.Binding and Bioeffects of Ipriflavone on a human preosteoclastic cell line[J].Biochem Biophys Res,1994,201:1080~1089.
[2]冯坤,刘月桂,张灵菊,等.高转换型骨质疏松模型生化特点[J].中国骨质疏松杂志,1997 3(2):25.
[3]Bonucci E.Ipriflavone inhibits osteoclast differentiation in parathyroid transplanted parietal bone of rats[J].Calcif Tissue Int,1992,50:314-319.
[4]Valimaki M L,Tahtela R,Jones J D,et al.Bone resorption in healthy and osteoporosis postmenopausal women:comparison marker for serum carboxyterminal telopeptide of type I college and urinary pyridinium cross-lines[J].Eur J Endocrinol,1994,131:258-262.
[5]Robert L,Giuseppe G.Increased osteoclast development after estrogen loss:mediation by IL-6[J].Science,1992,527:88.
[6]Hiroshi M,Yoshi yuki H,Nobuhiko W.IGF-1 support formation and activation of osteoclasts[J].Endocrinology,1992,131:1075-1080.
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脚注
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