Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
Eur Rev Med Pharmacol Sci. 2021 May;25(9):3546-3556. doi: 10.26355/eurrev_202105_25837.
The aim of the present study was to compare the molecular and morphological effects of diacerein and glucosamine-chondroitin drug treatment and intra-articular injection therapy of human deciduous dental pulp stem cells (hDPSCs) in a rat knee model of induced osteoarthritis (OA).
Thirty-six adult male rats were randomly separated into six groups: Control group (without induction of OA), osteoarthritis group 60 (induction of OA, saline gavage started on day 14 and performed for 60 days, followed by euthanasia), osteoarthritis group (induction of OA and euthanasia after 14 days), diacerein group, glucosamine-chondroitin group, and mesenchymal stem cell group. The drug-treated groups were gavaged with 50 mg/kg of diacerein and 400/500 mg/kg of glucosamine-chondroitin starting on dat 14 for 60 days. The cell therapy-treated group received an intra-articular single dose of 8 × 105 hDPSCs on day 14, and euthanasia was performed after 60 days. Lateral femoral condyles were collected and prepared for immunohistochemistry and light microscopy procedures.
The morphological features and immunoexpression of SOX-5, IHH, MMP-8, MMP-13, and Type II collagen were statistically analysed. Our data suggest that hDPSC therapy contributes more actively and effectively in the structural reorganization of lateral femoral condyles. In contrast, the glucosamine-chondroitin sulphate treatment was more effective in inflammatory control, while diacerein showed better results associated with the maintenance of the primordial cartilage.
The positive therapeutic effect of daily administered conventional drugs can be confirmed in a rat model of OA. However, one single dose of locally administered hDPSCs provides significant improvement in tissue regeneration in an OA model.
本研究旨在比较二乙酰氨己酸和氨基葡萄糖-软骨素药物治疗以及关节内注射人乳牙牙髓干细胞(hDPSCs)对诱导性骨关节炎(OA)大鼠膝关节模型的分子和形态影响。
36 只成年雄性大鼠随机分为 6 组:对照组(不诱导 OA)、OA 组 60 只(诱导 OA,第 14 天开始灌胃生理盐水,持续 60 天,然后安乐死)、OA 组(诱导 OA,第 14 天安乐死)、二乙酰氨己酸组、氨基葡萄糖-软骨素组和间充质干细胞组。药物治疗组从第 14 天开始灌胃 50mg/kg 二乙酰氨己酸和 400/500mg/kg 氨基葡萄糖-软骨素,持续 60 天。细胞治疗组于第 14 天单次关节内注射 8×105 hDPSCs,60 天后安乐死。收集外侧股骨髁并准备进行免疫组织化学和光镜程序。
对 SOX-5、IHH、MMP-8、MMP-13 和 II 型胶原的形态特征和免疫表达进行了统计分析。我们的数据表明,hDPSC 治疗更积极有效地促进了外侧股骨髁的结构重排。相比之下,氨基葡萄糖-软骨素硫酸盐治疗在炎症控制方面更有效,而二乙酰氨己酸在维持原始软骨方面表现出更好的效果。
在 OA 大鼠模型中,证实了常规药物的每日给药的积极治疗效果。然而,单次局部给予 hDPSCs 可显著改善 OA 模型中的组织再生。