Nanoplatforms for Promoting Osteogenesis in Ovariectomy-Induced Osteoporosis in the Experimental Model

Q3 Medicine
Enas A. Fouad-Elhady, H. Aglan, Rasha E. Hassan, Gilane M. Sabry, H. Ahmed
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Abstract

Osteoporosis is a bone-debilitated ailment characterized by obvious bone mass loss and bone microarchitecture impairment. This study was tailored to illuminate the in vivo usefulness of nanotechnology as an osteoporosis treatment via analyzing the effectiveness of nano-hydroxyapatite (nHa), nano-hydroxyapatite/chitosan (nHa/C) and nano-hydroxyapatite/silver (nHa/S) in mitigation of osteoporosis in ovariectomized rats. The characterization of the nHa, nHa/C and nHa/S was carried out using TEM, SEM, FTIR and Zeta potential measurements. This in vivo study included 48 adult female rats that were randomized into six groups (8 rats/group): (1) Sham-operated control, (2) osteoporotic, (3) nHa, (4) nHa/C, (5) nHa/S and (6) Fosamax®. Serum Osterix level was quantified using ELISA. Femur bone morphogenetic protein 2 and SMAD1 mRNA levels were evaluated by qPCR. The femur bones were scanned by DEXA for measurement of bone mineral density and bone mineral content. In addition, histopathological examination of femur bones was performed. The present approach denoted that the treatment with nHa, nHa/C or nHa/S yields significant rise in serum level of Osterix and mRNA levels of bone morphogenetic protein 2 and SMAD1 as well as significant enhancements of bone tissue minerals. The findings affirmed the potency of nHa, nHa/C and nHa/Sas an auspicious nanoplatforms for repairing bone defects in the osteoporotic rat model. The positive effect of the inspected nanoformulations arose from the motivation of bone formation indicators in serum and tissue, additionally the reinforcement of bone density and content which was verified by the histopathological description of bone tissue sections.
纳米平台促进卵巢切除所致骨质疏松症成骨的实验模型
骨质疏松症是一种骨衰弱性疾病,其特征是明显的骨量损失和骨微结构损伤。本研究旨在通过分析纳米羟基磷灰石(nHa)、纳米羟基磷灰石/壳聚糖(nHa/C)和纳米羟基磷灰石/银(nHa/S)在减轻去卵巢大鼠骨质疏松症方面的有效性,阐明纳米技术作为骨质疏松症治疗的体内有用性。利用TEM、SEM、FTIR和Zeta电位测量对nHa、nHa/C和nHa/S进行了表征。这项体内研究包括48只成年雌性大鼠,它们被随机分为六组(8只大鼠/组):(1)假手术对照组,(2)骨质疏松组,(3)nHa,(4)nHa/C,(5)nHa/S和(6)Fosamax®。使用ELISA对血清Osterix水平进行定量。通过qPCR评估股骨形态发生蛋白2和SMAD1 mRNA水平。用DEXA扫描股骨,测量骨密度和骨矿物质含量。此外,还对股骨进行了组织病理学检查。本方法表明,用nHa、nHa/C或nHa/S治疗可显著提高Osterix的血清水平和骨形态发生蛋白2和SMAD1的mRNA水平,并显著增强骨组织矿物质。研究结果证实了nHa、nHa/C和nHa/Sas作为一种有益的纳米平台在骨质疏松大鼠模型中修复骨缺损的潜力。所检查的纳米制剂的积极作用源于血清和组织中骨形成指标的动机,此外,骨密度和含量的增强,骨组织切片的组织病理学描述证实了这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Nanomedicine
Current Nanomedicine Medicine-Medicine (miscellaneous)
CiteScore
2.00
自引率
0.00%
发文量
15
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