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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Ethanolic extract of Dalbergia sissoo promotes rapid regeneration of cortical bone in drill-hole defect model of rat
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Ethanolic extract of Dalbergia sissoo promotes rapid regeneration of cortical bone in drill-hole defect model of rat

机译:达伯尔加氏菌乙醇提取物促进了大鼠钻孔缺损模型中皮质骨的快速再生

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摘要

Leaves of Dalbergia sissoo is known to have protective actions against postmenopausal bone loss in rat. In this study, we have evaluated the fracture healing properties of ethanolic extract (EE) of Dalbergia sissoo leaves. To observe the fracture healing property in the drill-hole injury model, we randomly divided total 32 adult female Sprague Dawley rats (180 +/- 200 g) into 4 groups: (i) Control operated group; (ii) EE (250 mg/kg/day); (iii) EE (500 mg/kg/day) and (iv) EE (1000 mg/kg/day). The right femora were fractured at the mid-diaphysis region and each group of rats received their respective treatment for 15 days. Ethanol extract dose dependently induced bone regeneration at the fracture site assessed by fluorochrome labeling. All of three doses, 250 mg/kg/day dose significantly increased bone volume fraction, trabecular thickness, trabecular number, and connectivity density and decreased trabecular separation in bone. Furthermore, the extract induced the expression of osteogenic genes including BMP2, BMP-4, RunX-2 and COL-1 compared to the control group. The EE improved fracture healing much earlier (day 15) than the normal healing process, as assessed by the increased callus volumes and mineralized nodule formation. This extract is found beneficial in fracture healing of rat. (C) 2016 Elsevier Masson SAS. All rights reserved.
机译:众所周知,达伯利亚叶片的叶子对大鼠绝经后骨质损失具有保护作用。在这项研究中,我们评估了达伯利亚叶片乙醇萃取物(EE)的骨折愈合特性。要观察钻孔损伤模型中的骨折愈合性能,我们将32名成人女性Sprague Dawley大鼠(180 +/- 200g)随机分为4组:(i)控制经营组; (ii)ee(250 mg / kg /天); (III)EE(500mg / kg /天)和(iv)ee(1000mg / kg /天)。右股骨在中间晶体分裂区域处裂缝,每组大鼠接受其各自的治疗15天。乙醇萃取剂量依赖于荧光染料标记评估的骨折位点诱导骨再生。所有三剂量,250mg / kg /天剂量显着增加骨体积分数,骨粗厚度,小梁数和连接密度,并且在骨中减少了小梁分离。此外,与对照组相比,提取物诱导包括BMP2,BMP-4,RUNX-2和COL-1的骨质原基因的表达。 EE改善了骨折愈合(第15天),而不是正常愈合过程,如增加的愈伤组织体积和矿化结节形成。发现该提取物有益于大鼠的骨折愈合。 (c)2016 Elsevier Masson SAS。版权所有。

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