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首页> 外文期刊>Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA >Basic fibroblast growth factor forms new trabeculae that physically connect with pre-existing trabeculae, and this new bone is maintained with an anti-resorptive agent and enhanced with an anabolic agent in an osteopenic rat model.
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Basic fibroblast growth factor forms new trabeculae that physically connect with pre-existing trabeculae, and this new bone is maintained with an anti-resorptive agent and enhanced with an anabolic agent in an osteopenic rat model.

机译:碱性成纤维细胞生长因子形成新的骨小梁,与先前存在的骨小梁物理连接,在骨质减少的大鼠模型中,这种新骨被抗吸收剂维持并被合成代谢剂增强。

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摘要

Osteoporosis is a disease of excess bone fragility that results from both the loss of bone mass and trabecular bone microarchitecture, thereby creating a very fragile skeleton. The purpose of this study was to determine whether treatment of ovariectomized (OVX) osteopenic rats with basic fibroblast growth factor (bFGF) would stimulate the production of new trabeculae, and whether the newly formed trabeculae would make physical connections with the pre-existing trabeculae after prolonged estrogen deficiency. Six-month-old Sprague Dawley rats were OVXed or sham-operated and were left untreated until day 60 post-OVX. A high resolution microscopic scan (XTM) of the right proximal tibia was performed on groups 1 and 2 on day 1 post-OVX, and was repeated in all animals on day 60 post-OVX. At day 60 groups 1 and 2 were treated with vehicle and groups 3 to 6 were injected with bFGF 200 microg/kg/d intravenously for 15 days. At day 82, all animals obtained another in vivo XTM scan of the right tibia; then group4 were treated with 17B estradiol 10 microg/kg/3x a week, group 5 were treated with hPTH (1-34) at 80 microg/kg/d for 35 days, group 6 were sacrificed, and groups 1 and 2 were treated with vehicle injections for 35 days. At day 110, all remaining animals were sacrificed, and repeat ex vivo XTM scans of the right proximal tibia were performed. Trabecular bone structural variables-including trabecular bone volume, connectivity, number, and thickness-were obtained from all XTM scans. Biochemical markers of bone turnover were also obtained 24 hours before each XTM scan (osteocalcin and deoxypyridinoline), and analyzed by ELISA. Animals OVXed and treated with vehicle had decreased trabecular bone volume, connectivity and number compared to sham-operated animals at both day 60 and day 110. Animals treated with bFGF from day 60-75 post-OVX had evidence of new trabeculae that physically connected with pre-existing trabeculae and also of increased trabecular bone volume seven days after the injections were discontinued. Biochemical markers of bone formation had a small and insignificant increase over baseline levels during the bFGF injections. Bone resorption markers were significantly reduced during the injection period, but returned to baseline levels after the injections were stopped. In addition, we also demonstrated that these newly formed trabecular connections could be maintained or added to with either estrogen or hPTH (1-34) treatments. Thirty-five days after ending the bFGF treatment, trabecular bone volume and connectivity was 25-80% higher in the estrogen and hPTH (1-34) treated animals compared to the untreated animals ( p<0.01). These results support continued development of bFGF as a potential treatment for severely osteoporotic individuals.
机译:骨质疏松症是骨质流失过多的一种疾病,它是由于骨量的损失和小梁骨微结构导致的,从而形成了非常脆弱的骨骼。这项研究的目的是确定用碱性成纤维细胞生长因子(bFGF)治疗去卵巢(OVX)骨质疏松大鼠是否会刺激新的小梁的生成,以及新形成的小梁在术后是否会与先前存在的小梁发生物理连接长期雌激素缺乏症。对六个月大的Sprague Dawley大鼠进行OVX或假手术,直到OVX后第60天才接受治疗。在OVX后第1天对第1组和第2组进行右胫骨近端高分辨率显微镜扫描(XTM),并在OVX后第60天在所有动物中重复进行。在第60天,第1和第2组用媒介物治疗,第3至第6组静脉注射bFGF 200 microg / kg / d,持续15天。在第82天,所有动物都进行了右胫骨的另一次体内XTM扫描。然后第4组每周用10μg/ kg / 3x的17B雌二醇治疗,第5组以80 microg / kg / d用hPTH(1-34)治疗35天,处死第6组,第1和第2组进行治疗用车辆注射35天。在第110天,处死所有剩余的动物,并对右胫骨近端进行离体XTM重复扫描。从所有XTM扫描中获取小梁骨结构变量,包括小梁骨体积,连接性,数量和厚度。还可以在每次XTM扫描前24小时(骨钙蛋白和脱氧吡啶并啉)获得骨转换的生化标志物,并通过ELISA分析。与假手术动物相比,用OVX进行处理并用赋形剂处理的动物的骨小梁骨体积,连通性和数量均减少。从OVX后60-75天用bFGF治疗的动物有新的骨小梁与骨物理连接的证据。停止注射后7天,原有的小梁以及小梁的骨量增加。在bFGF注射过程中,骨形成的生化标志物与基线水平相比有很小的微不足道的增加。在注射期间,骨吸收标记物显着减少,但在停止注射后恢复到基线水平。此外,我们还证明了这些新形成的小梁连接可以通过雌激素或hPTH(1-34)治疗得以维持或增加。结束bFGF治疗后的第35天,与未治疗的动物相比,雌激素和hPTH(1-34)治疗的动物的小梁骨体积和连接性高25-80%(p <0.01)。这些结果支持bFGF的持续开发,可作为严重骨质疏松症个体的潜在治疗方法。

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