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 >The effects of combined human parathyroid hormone (1-34) and zoledronic acid treatment on fracture healing in osteoporotic rats.
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The effects of combined human parathyroid hormone (1-34) and zoledronic acid treatment on fracture healing in osteoporotic rats.

机译:人甲状旁腺激素(1-34)和唑来膦酸联合治疗对骨质疏松大鼠骨折愈合的影响。

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摘要

Ovariectomized (OVX) rats with tibial fracture received vehicle, ZA, PTH, or ZA plus PTH treatment for 4 and 8 weeks. Bone metabolism, callus formation, and the mass of undisturbed bone tissue were evaluated by serum analysis, histology, immunohistochemistry, radiography, micro-computerized tomography, and biomechanical test.Previous studies have demonstrated the effect of ZA or PTH on osteoporotic fracture healing. However, reports about effects of ZA plus PTH on callus formation of osteoporotic fracture were limited. This study was designed to investigate the impact of combined treatment with ZA and PTH on fracture healing in OVX rats.Twelve weeks after bilateral ovariectomy, all rats underwent unilateral transverse osteotomy on tibiae. Animals then randomly received vehicle, ZA (1.5 μg/kg weekly), PTH (60 μg/kg, three times a week), or ZA plus PTH until death at 4 and 8 weeks. The blood and bilateral tibiae of rats were harvested for evaluation.All treatments increased callus formation and strength other than the control; ZA + PTH showed the strongest effects on percent bone volume (BV/TV), trabecular thickness, total fluorescence-marked callus area, and biomechanical strength. Additionally, inhibited RANKL and enhanced osteoprotegerin expression were observed in the ZA + PTH group. But no difference in bone mineral density and BV/TV of the contralateral tibiae was observed between treated groups.Findings in this study suggested an additive effect of ZA and PTH on fracture healing in OVX rats, and this additive effect was specific to callus formation, not to undisturbed bone tissue.
机译:接受卵巢切除术(OVX)的胫骨骨折大鼠接受媒介物,ZA,PTH或ZA加PTH治疗4周和8周。通过血清分析,组织学,免疫组织化学,放射线照相,微型计算机断层扫描和生物力学测试评估了骨代谢,骨us形成和未受干扰的骨组织的质量。先前的研究已证明ZA或PTH对骨质疏松性骨折愈合的影响。然而,关于ZA加PTH对骨质疏松性骨折的愈伤组织形成的影响的报道有限。本研究旨在探讨ZA和PTH联合治疗对OVX大鼠骨折愈合的影响。双侧卵巢切除术后十二周,所有大鼠均在胫骨上进行了单侧横向截骨术。然后,动物随机接受赋形剂,ZA(每周1.5μg/ kg),PTH(60μg/ kg,每周3次)或ZA加PTH,直到第4和8周死亡。收集大鼠的血液和双侧胫骨进行评估。除对照组外,所有处理均增加了愈伤组织的形成和强度。 ZA + PTH对骨体积百分比(BV / TV),小梁厚度,荧光标记的愈伤组织总面积和生物力学强度影响最大。此外,在ZA + PTH组中观察到了抑制的RANKL和增强的骨保护素表达。但治疗组之间未观察到对侧胫骨的骨矿物质密度和BV / TV差异。本研究发现,ZA和PTH对OVX大鼠骨折愈合有累加作用,且该累加作用特定于愈伤组织的形成,不要破坏骨组织。

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