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透明质酸-壳聚糖-曲安奈德-β-环糊精复合物对人软骨细胞的活力和抗炎作用。

The Viability and Anti-Inflammatory Effects of Hyaluronic Acid-Chitlac-Tracimolone Acetonide- β-Cyclodextrin Complex on Human Chondrocytes.

机构信息

Department of Molecular Medicine, Histology Unit, University of Padova, Padova, Italy.

Musculoskeletal Pathology and Oncology Laboratory, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

出版信息

Cartilage. 2021 Dec;13(2_suppl):920S-924S. doi: 10.1177/1947603520908658. Epub 2020 Feb 28.

DOI:10.1177/1947603520908658
PMID:32107923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8804853/
Abstract

OBJECTIVE

To compare the effects of the complex triamcinolone acetonide-hydroxypropyl-β-cyclodextrin (TA-CD) on inflamed primary human articular chondrocytes in the presence or absence of the mixture hyaluronic acid-Chitlac, a lactose-modified chitosan (HA-CTL).

DESIGN

Changes in cell viability and pro-inflammatory cytokines gene expression were analyzed in human chondrocytes using an model of macrophage-mediated inflammation. Human monocytes U937 were differentiated to macrophages by phorbol 12-myristate 13-acetate (PMA) and lipopolysaccharides (LPS). The anti-inflammatory effects of the complex TA-CD and HA-CTL mixture were assessed on chondrocytes exposed for 24 hours to U937 conditioned medium (CM), by quantitative polymerase chain reaction analysis.

RESULTS

The TA-CD viability was enhanced by the presence of the HA-CTL mixture in chondrocyte cultures. The exposure of cells to CM significantly increased interleukin-1β and interleukin-6 gene expression, and when the complex TA-CD was added to the inflamed cells, gene transcription of cytokines was restored to near baseline values, both in the presence or in the absence of HA-CTL mixture.

CONCLUSION

The addition of HA-CTL mixture significantly attenuated cytotoxicity induced by TA and preserved the anti-inflammatory effects, thus confirming the chondroprotective role of the HA-CTL mixture.

摘要

目的

比较曲安奈德-羟丙基-β-环糊精(TA-CD)复合物在存在或不存在透明质酸-壳聚糖(HA-CTL)混合物的情况下对原代人关节软骨细胞炎症的影响。

设计

使用巨噬细胞介导的炎症模型分析人软骨细胞中细胞活力和促炎细胞因子基因表达的变化。用佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)和脂多糖(LPS)将人单核细胞 U937 分化为巨噬细胞。通过定量聚合酶链反应分析,评估 TA-CD 复合物和 HA-CTL 混合物在暴露于 U937 条件培养基(CM)24 小时的软骨细胞中的抗炎作用。

结果

在软骨细胞培养物中,HA-CTL 混合物的存在增强了 TA-CD 的活力。细胞暴露于 CM 会显著增加白细胞介素 1β 和白细胞介素 6 基因的表达,而当将 TA-CD 复合物添加到炎症细胞中时,细胞因子的基因转录被恢复到接近基线值,无论是否存在 HA-CTL 混合物。

结论

添加 HA-CTL 混合物可显著减轻 TA 诱导的细胞毒性,并保留抗炎作用,从而证实了 HA-CTL 混合物的软骨保护作用。

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