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枸橼酸氯米芬对大鼠注射促黄体生成素释放激素激动剂引发的雌激素缺乏性骨质减少的预防作用。

Preventive effects of clomiphene citrate on estrogen-deficiency osteopenia elicited by LHRH agonist administration in the rat.

作者信息

Goulding A, Fisher L

机构信息

Department of Medicine, University of Otago, Dunedin, New Zealand.

出版信息

J Bone Miner Res. 1991 Nov;6(11):1177-81. doi: 10.1002/jbmr.5650061106.

Abstract

The estrogen agonist and antagonist clomiphene citrate has been shown to prevent bone loss induced by ovariectomy in the rat. In young women estrogen-deficiency bone loss is a clinical problem associated with the use of luteinizing hormone releasing hormone (LHRH) agonists, such as buserelin, to treat endometriosis. The aim of this study was to determine whether clomiphene citrate (10 mg/kg body weight per week orally) would prevent the osteopenic effect of buserelin (25 micrograms/kg body weight per day SC) in the rat. Four groups of animals with 45Ca-labeled skeletons were studied for 4 weeks: group A, placebo controls; group B, buserelin; group C, clomiphene; and group D, buserelin + clomiphene. Bone resorption was monitored by measuring the urinary excretion of 45Ca and hydroxyproline. Clomiphene slowed bone breakdown and inhibited the osteopenic effect of buserelin. Total-body calcium values (mean +/- SD) were (mg) 2635 +/- 181, 2267 +/- 85, 2566 +/- 126, and 2624 +/- 77 in groups A to D, respectively. Osteopenia was present only in group B (P less than 0.001). Interestingly buserelin lowered blood 17 beta-estradiol and uterine weights to a similar extent in the presence and absence of clomiphene. Because clomiphene inhibited estrogen-deficiency bone loss in buserelin-treated rats without depressing the hypoestrogenic action of this LHRH agonist, it is suggested that the use of clomiphene to protect the skeleton during LHRH agonist therapy of endometriosis warrants further study.

摘要

雌激素激动剂和拮抗剂枸橼酸氯米芬已被证明可预防大鼠卵巢切除术后引起的骨质流失。在年轻女性中,雌激素缺乏性骨质流失是一个临床问题,与使用促黄体生成素释放激素(LHRH)激动剂(如布舍瑞林)治疗子宫内膜异位症有关。本研究的目的是确定枸橼酸氯米芬(每周口服10mg/kg体重)是否能预防布舍瑞林(每天皮下注射25μg/kg体重)对大鼠的骨质减少作用。对四组带有45Ca标记骨骼的动物进行了为期4周的研究:A组为安慰剂对照组;B组为布舍瑞林组;C组为氯米芬组;D组为布舍瑞林+氯米芬组。通过测量45Ca和羟脯氨酸的尿排泄量来监测骨吸收。氯米芬减缓了骨分解,并抑制了布舍瑞林的骨质减少作用。A组至D组的全身钙值(平均值±标准差)分别为(mg)2635±181、2267±85、2566±126和2624±77。只有B组出现了骨质减少(P<0.001)。有趣的是,无论有无氯米芬,布舍瑞林都会使血液中17β-雌二醇和子宫重量降低到相似程度。由于氯米芬在布舍瑞林治疗的大鼠中抑制了雌激素缺乏性骨质流失,而没有抑制这种LHRH激动剂的低雌激素作用,因此建议在子宫内膜异位症的LHRH激动剂治疗期间使用氯米芬保护骨骼值得进一步研究。

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