The Validation of an Experimental Model in Wistar Female Rats to Study Osteopenia and Osteoporosis.

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Artur Lage Pedroso, Raul Canal, Sergio Alexandre Gehrke, Eleani Maria da Costa, Antonio Scarano, Fernanda Barchesi Zanelatto, André Antonio Pelegrine
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Abstract

Background: Osteoporosis is a systemic disease characterized by a progressive decrease in bone density and deterioration of the tissue's microarchitecture. This results in greater structural fragility and a higher risk of fractures. Osteopenia represents the beginning of the process of decreasing bone density and, if left untreated, can lead to osteoporosis. The objective of this study was to validate an experimental model for establishing cases of decreased bone density that allows for the creation of different levels of severity of mineral loss and changes in bone microstructure. Materials and Methods: Twenty female Wistar rats, 12 weeks old and with a body weight ranging from 300 to 400 g, were used in this study. The animals were randomly distributed into five groups (n = 5 per group): a control group (CG), where the animals were not ovariectomized (OVX), and four experimental groups, where the animals were OVX and euthanized at different times: 30 days (G30), 40 days (G40), 60 days (G60), and 80 days (G80). The animals in the experimental groups underwent bilateral ovariectomy to induce mineral loss. The femurs were collected after the periods established for each group and analyzed using microcomputed tomography (μCT) to determine bone density and count the number of trabeculae. Furthermore, the T-score was calculated for each group. Results: There were significant differences in bone density when comparing all groups, with GC > G30 > G40 > G60 > G80. For the number of trabeculae, GC presented more trabeculae than all other groups. More trabeculae were also observed in G30 when compared to G40, G60, and G80; however, there were no differences between G40, G60, and G80. Regarding the calculation of the T-score by group, osteopenia was observed in G30 (T-score: -2.42) and osteoporosis was observed in G40, G60, and G80 (T-scores: -4.38, -6.34, and -7.71, respectively). Conclusions: The results demonstrate that ovariectomy induces progressive changes in bone structure, with the onset of osteopenia 30 days after ovariectomy and osteoporosis after 40 days in this experimental model. These results may aid future investigations that seek to focus on the specific treatment of osteopenia and/or osteoporosis.

Wistar雌性大鼠骨质减少与骨质疏松实验模型的验证。
背景:骨质疏松症是一种全身性疾病,其特征是骨密度进行性降低和组织微结构恶化。这导致更大的结构脆弱性和更高的骨折风险。骨质减少是骨密度下降过程的开始,如果不及时治疗,可导致骨质疏松症。本研究的目的是验证一个实验模型,用于建立骨密度降低的病例,该模型允许创建不同程度的矿物质流失严重程度和骨微观结构的变化。材料与方法:选用雌性Wistar大鼠20只,12周龄,体重300 ~ 400 g。随机分为5组(每组n = 5):对照组(CG)不切除卵巢(OVX),实验组(OVX),分别在30天(G30)、40天(G40)、60天(G60)、80天(G80)的不同时间对动物实施安乐死。实验组采用双侧卵巢切除术诱导矿物质流失。各组术后取股骨,采用微计算机断层扫描(μCT)测定骨密度,计数骨小梁数。进一步,计算各组的t得分。结果:各组骨密度比较差异有统计学意义,GC > G30 > G40 > G60 > G80。小梁数目方面,GC组小梁数目多于其他各组。与G40、G60和G80相比,G30中也观察到更多的小梁;然而,G40、G60和G80之间没有差异。分组计算t评分时,G30组出现骨质减少(t评分为-2.42),G40、G60、G80组出现骨质疏松(t评分分别为-4.38、-6.34、-7.71)。结论:实验结果表明,卵巢切除引起骨结构进行性改变,卵巢切除后30 d出现骨质减少,40 d出现骨质疏松。这些结果可能有助于未来针对骨质减少和/或骨质疏松症特异性治疗的研究。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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