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阿仑膦酸盐通过抑制钙化软骨的吸收,增加生长中大鼠在失重状态下的骨骼质量。

Alendronate increases skeletal mass of growing rats during unloading by inhibiting resorption of calcified cartilage.

作者信息

Bikle D D, Morey-Holton E R, Doty S B, Currier P A, Tanner S J, Halloran B P

机构信息

Department of Medicine, University of California, San Francisco.

出版信息

J Bone Miner Res. 1994 Nov;9(11):1777-87. doi: 10.1002/jbmr.5650091115.

Abstract

Loss of bone mass during periods of skeletal unloading remains an important clinical problem. To determine the extent to which resorption contributes to the relative loss of bone during skeletal unloading of the growing rat and to explore potential means of preventing such bone loss, 0.1 mg P/kg alendronate was administered to rats before unloading of the hindquarters. Skeletal unloading markedly reduced the normal increase in tibial mass and calcium content during the 9 day period of observation, primarily by decreasing bone formation, although bone resorption was also modestly stimulated. Alendronate not only prevented the relative loss of skeletal mass during unloading but led to a dramatic increase in calcified tissue in the proximal tibia compared with the vehicle-treated unloaded or normally loaded controls. Bone formation, however, assessed both by tetracycline labeling and by [3H]proline and 45Ca incorporation, was suppressed by alendronate treatment and further decreased by skeletal unloading. Total osteoclast number increased in alendronate-treated animals, but values were similar to those in controls when corrected for the increased bone area. However, the osteoclasts had poorly developed brush borders and appeared not to engage the bone surface when examined at the ultrastructural level. We conclude that alendronate prevents the relative loss of mineralized tissue in growing rats subjected to skeletal unloading, but it does so primarily by inhibiting the resorption of the primary and secondary spongiosa, leading to altered bone modeling in the metaphysis.

摘要

在骨骼失用期间骨量丢失仍然是一个重要的临床问题。为了确定在生长中的大鼠骨骼失用期间,骨吸收对骨相对丢失的影响程度,并探索预防这种骨丢失的潜在方法,在大鼠后肢失用前给予0.1mg磷/千克阿仑膦酸盐。在9天的观察期内,骨骼失用显著降低了胫骨质量和钙含量的正常增加,主要是通过减少骨形成,尽管骨吸收也受到适度刺激。与用赋形剂处理的失用或正常加载的对照相比,阿仑膦酸盐不仅防止了失用期间骨骼质量的相对丢失,而且导致胫骨近端钙化组织显著增加。然而,通过四环素标记以及[3H]脯氨酸和45Ca掺入评估的骨形成受到阿仑膦酸盐处理的抑制,并因骨骼失用而进一步降低。在阿仑膦酸盐处理的动物中破骨细胞总数增加,但校正增加的骨面积后,其值与对照相似。然而,在超微结构水平检查时,破骨细胞的刷状缘发育不良,似乎未与骨表面接触。我们得出结论,阿仑膦酸盐可防止生长中遭受骨骼失用的大鼠矿化组织的相对丢失,但主要是通过抑制初级和次级骨小梁的吸收来实现,从而导致干骺端骨建模改变。

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