透明质酸在实验性骨关节炎模型中的关节内粘补充

Marcello Zaia Oliveira, Mauro Batista Albano, Guilherme Augusto Stirma, Mario Massatomo Namba, Leandro Vidigal, Luiz Antonio Munhoz da Cunha
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引用次数: 5

摘要

目的从免疫组化角度分析不同分子量透明质酸对兔骨关节炎实验模型的影响。方法将44只雄性加利福尼亚兔随机分为3组(PR、S、P),行右膝前交叉韧带切除术。术后3周,PR组注射低分子天然透明质酸(Hyalgan®),S组注射高分子支链透明质酸(Synvisc®),p组注射0.9%生理盐水,术后12周处死所有动物,解剖浸润膝关节的胫骨平台。用免疫组织化学标记对胫骨平台支撑区软骨组织切片进行染色,以研究金属蛋白酶(MMPs 3和13)及其抑制剂(TIMPs 1和3)的数量。在蔡司成像仪上定量染色强度。Z2 Metasystems显微镜和Metafer4 Msearch软件分析。结果与对照组相比,研究中使用的透明质酸的软骨保护作用得到证实。但在软骨保护方面,两组比较无统计学差异。结论在骨性关节炎模型中,生理盐水溶液有骨性关节炎发生的迹象,而添加天然低分子量透明质酸(Hyalgan®)和高分子量透明质酸(Synvisc®)对骨性关节炎模型的关节软骨有保护作用。
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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Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model

Objective

To analyze, from the immunohistochemical perspective, the effects of hyaluronic acid of different molecular weights in an experimental model of osteoarthritis in rabbits.

Methods

Forty-four male California rabbits were randomly assigned to three different groups (PR, S, and P) and submitted to the resection of the anterior cruciate ligament of the right knee. Three weeks after the surgical procedure, three intra-articular weekly injections were carried out with low-molecular-weight native hyaluronic acid (Hyalgan®) to PR group, high molecular weight branched chain hyaluronic acid (Synvisc®) to group S, and saline solution 0.9% to group P. All animals were sacrificed 12 weeks after the surgical procedure, and the tibial plateaus of the infiltrated knees were then dissected. Histological sections of cartilage from the tibial plateau support areas were stained with immunohistochemical markers in order to investigate the amount of metalloproteases (MMPs 3 and 13) and their inhibitors (TIMPs 1 and 3). The staining intensity was quantified on a Zeiss Imager.Z2 Metasystems microscope and analyzed by Metafer4 Msearch software.

Results

The chondroprotective effect of the hyaluronic acids used in the study was demonstrated when compared to the control group. However, the comparison between them presented no significant statistical difference regarding chondroprotection.

Conclusion

The injection of saline solution demonstrated signs of OA development, while adding native hyaluronic acid of low molecular weight (Hyalgan®) and hyaluronic acid of high molecular weight (Synvisc®) protected the articular cartilage in this model of OA.

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