Effects of zoledronic acid on bone structure and organization of nanocomposites in rats with obesity and limited mobility

IF 0.7 Cell Pathology Pub Date : 2021-01-01 DOI:10.1515/ersc-2021-0002
N. Kostyshyn, I. Shtablavyi
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Abstract

Abstract Background: Some investigations show that obesity is associated with increase in bone mass due to excessive mechanical exertion. However, these data are contradictory as loss of mineral density of bone tissue and, respectively, the risk of fractures in this population group is higher. The aim of the research was to investigate impact of drug therapy with zoledronic acid on nanostructure of bones in rats with limited mobility and high-calorie diet. Methods: Rats (n = 56) were distributed into three groups: control (n = 18) – standard vivarium conditions, І experimental group (n = 18) – rats, which were on a high-calorie diet with limited mobility (HCD+LM), ІІ experimental group (n = 18) – HCD+LM+zoledronic acid. Zoledronic acid was injected at the dose 0.025 mg/kg intramuscularly every four weeks for six months. X-ray structure analysis, scanning electron microscopy and atomic absorption spectrometry were used for investigation of ultrastructure and quantitative assessment of mineral component loss in the femoral neck. Results: Obesity and limited mobility reduced the level of the mineral component in the femoral neck (−31.5%) compared with control. It is significant that zoledronic acid did not permit decrease in mineral component of the bone throughout the entire experiment compared with group I (+41.8%), and all parameters were higher than in control group (+15%). Conclusions: Obesity and limited mobility negatively affect mineral bone mass. Zoledronic acid induces increase in the mineral component as a result of remodeling inhibition under conditions of obesity and limited mobility modeling.
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唑来膦酸对肥胖和活动受限大鼠骨结构和纳米复合材料组织的影响
背景:一些研究表明,肥胖与过度机械运动导致的骨量增加有关。然而,这些数据是相互矛盾的,因为骨组织矿物质密度的损失和骨折的风险在这一人群中更高。本研究旨在探讨唑来膦酸药物治疗对活动受限、高热量饮食大鼠骨骼纳米结构的影响。方法:将56只大鼠分为3组:对照组(n = 18) -标准体内条件,І实验组(n = 18) -高热量限行饮食大鼠(HCD+LM), ІІ实验组(n = 18) - HCD+LM+唑来膦酸。唑来膦酸以0.025 mg/kg的剂量肌注,每4周注射一次,连续6个月。采用x线结构分析、扫描电镜和原子吸收光谱法对股骨颈的超微结构进行研究,定量评价股骨颈矿物成分的流失情况。结果:与对照组相比,肥胖和活动受限降低了股骨颈矿物质成分水平(- 31.5%)。值得注意的是,唑来膦酸在整个实验过程中均未使骨矿物质成分降低(+41.8%),且各参数均高于对照组(+15%)。结论:肥胖和活动受限对矿物质骨量有负面影响。唑来膦酸诱导矿物成分的增加,作为肥胖和受限运动模型条件下重塑抑制的结果。
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