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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Accretion of bone mass and strength with parathyroid hormone prior to the onset of estrogen deficiency can provide temporary beneficial effects in skeletally mature rats.
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Accretion of bone mass and strength with parathyroid hormone prior to the onset of estrogen deficiency can provide temporary beneficial effects in skeletally mature rats.

机译:在雌激素缺乏症发作之前,甲状旁腺激素可增加骨量和强度,可为骨骼成熟的大鼠提供暂时的有益作用。

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摘要

Intermittent administration of parathyroid hormone (PTH) has been shown to be an anabolic agent for animal and human skeletons. In previous studies, PTH has been used concurrent with, or subsequent to, the onset of bone loss. However, it is entirely possible that PTH may be used as an anabolic agent in a situation where there is stable skeletal remodeling. Increasing bone mass at this time might confer long-lasting beneficial effects when bone loss begins, for example, subsequent to the loss of ovarian function. To test this hypothesis, we evaluated the effects of administering rat PTH(1-34) (80 microg/kg/day, subcutaneously [s.c.]) to 6-month-old rats for a 2-week period prior to ovariectomy, and followed the natural occurrence of bone loss over a 14-week period. To determine the effects of estrogen intervention on bone gained by PTH treatment, one group was repleted with 17beta-estradiol (10 microg/kg/day via s.c. implant). Serial measurements of bone mass in vivo at the distal femur were obtained at 2-week intervals using dual-energy X-ray absorptiometry, while histologic and mechanical strength data were obtained from excised proximal tibiae and distal femurs after sacrifice. Two weeks of PTH treatment resulted in an increase of bone mineral density (BMD), mechanical strength, and cancellous bone volume (CnBV/TV). Four weeks after PTH withdrawal, significant residual beneficial effects on BMD and strength, irrespective of ovarian status, were observed. However, 14 weeks after PTH withdrawal, although there were still residual effects on CnBV/TV in ovariectomized animals pretreated with PTH, the PTH effects on BMD and mechanical strength had been lost. Estradiol repletion during the rapid bone loss phase following ovariectomy prevented the reduction in BMD associated with either ovariectomy or PTH withdrawal. Our results suggest that: treatment of rats with PTH prior to ovariectomy produces an increase in BMD and strength, these beneficial effects extend for a period of at least three times the treatment duration, the BMD that is lost when PTH is discontinued equates to the amount accrued during the PTH treatment, estrogen replacement can be used to maintain the bone gained as a result of PTH treatment.
机译:甲状旁腺激素(PTH)的间歇给药已被证明是动物和人类骨骼的合成代谢药物。在先前的研究中,PTH与骨质流失同时发生或在骨质疏松发生之后一起使用。但是,在稳定的骨骼重塑的情况下,完全有可能将PTH用作合成代谢药物。此时,例如在卵巢功能丧失之后开始骨质流失时,增加骨量可能会带来长期的有益效果。为了验证该假设,我们评估了在卵巢切除术之前2周内对6个月大的大鼠施用大鼠PTH(1-34)(80 microg / kg /天,皮下[sc])的效果,在14周内自然发生骨质流失。为了确定雌激素干预对通过PTH治疗获得的骨的影响,一组中补充了17β-雌二醇(经皮下植入的剂量为10微克/千克/天)。使用双能X线骨密度仪以2周为间隔获取一系列在股骨远端的体内骨量,同时从处死后的胫骨近端和股骨远端获得组织学和机械强度数据。 PTH治疗两周导致骨矿物质密度(BMD),机械强度和松质骨体积(CnBV / TV)升高。停用PTH后四周,无论卵巢状况如何,均观察到对BMD和强度的显着残余有益作用。然而,撤消PTH后14周,尽管在用PTH预处理的去卵巢动物中对CnBV / TV仍有残留影响,但PTH对BMD和机械强度的影响已经消失。卵巢切除术后快速骨质疏松期的雌二醇补充可防止与卵巢切除术或PTH停药有关的BMD降低。我们的结果表明:在卵巢切除术之前用PTH对大鼠进行治疗会产生BMD和强度的增加,这些有益作用的持续时间至少是治疗持续时间的三倍,因此中断PTH时失去的BMD等于在PTH治疗期间产生的雌激素替代物可用于维持因PTH治疗而获得的骨骼。

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