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作 者:葛志东[1] 周爱武[1] 王迎新[2] 李卫平[1] 李康 王斌[1] 姚余有[1] 陈敏珠[1]
机构地区:[1]安徽医科大学临床药理研究所,合肥230032 [2]安徽省卫生干部进修学校,合肥230001 [3]安徽中医学院药学系
出 处:《中国药理学通报》1997年第5期447-449,共3页Chinese Pharmacological Bulletin
摘 要:目的研究国产依扑拉芬对大鼠骨质疏松的影响。方法:使用维甲酸诱导大鼠骨质疏松。结果:依扑拉芬显著降低维甲酸升高的尿Ca(2+)排泄量,显著升高血Ca(2+)浓度。逆转维甲酸降低的血pi浓度,剂量依赖性增加维甲酸降低的股骨干骺端和骨干的平均骨密度,显著升高维甲酸降低的股骨Ca(2+)和Pi含量。结论:依扑拉芬对维甲酸引起的大鼠骨质疏松具有良好的防治作用。Effect of ipriflavone on vita-min A acid-induced osteoporosis in rats wasstudied. METHODS: Vitamin A acid was usedto induce osteoporosis in rats. RESUCTS: Vita-min A acid 70 mg. kg-1. d-1 markedly decreased the calcium and phosphorus contents offemora, and serum phosphorus, and significantly increased uninary calcium. Microdensitometrical analysis of roentgenography indicatedthat vitamin A acid 70 mg. kg-1. d-1 noticeablyreduced the density of both distal metaphysesand diaphyses of femora. When ipriflavone atthe doses of 50, 100, 200 mg. kg-1. d-1 wasintragastrically administered to rats, it wasfound that the above-mentioned changes inducedby vitamin A acid were dose-dependently inhibited. In addition, ipriflavone at the doses of 50.100, 200 mg. kg-1'. d-1 showed marked elevating effect on serum calcium in rats. CONCLUSION: Ipriflavone is effective in preventing andtreating osteoporosis in rats induced by vitaminA acid.
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