首页> 美国卫生研究院文献>International Scholarly Research Notices >Andrographolide Exerts Chondroprotective Activity in Equine Cartilage Explant and Suppresses Interleukin-1β-Induced MMP-2 Expression in Equine Chondrocyte Culture
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Andrographolide Exerts Chondroprotective Activity in Equine Cartilage Explant and Suppresses Interleukin-1β-Induced MMP-2 Expression in Equine Chondrocyte Culture

机译:穿心莲内酯在马软骨外植体中具有软骨保护活性并抑制白细胞介素1β诱导的马软骨细胞培养物中MMP-2的表达。

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摘要

Cartilage erosion in degenerative joint diseases leads to lameness in affected horses. It has been reported that andrographolide from Andrographis paniculata inhibited cartilage matrix-degrading enzymes. This study aimed to explore whether this compound protects equine cartilage degradation in the explant culture model and to determine its effect on matrix metalloproteinase-2 (MMP-2) expression, a matrix-degrading enzyme, in equine chondrocyte culture. Equine articular cartilage explant culture was induced by 25 ng/mL interleukin-1β, a key inducer of cartilage degeneration, in cultures with or without andrographolide ranging from 10 to 50 μM. After 3–21 days, they were analyzed for the markers of cartilage degradation. It was found that interleukin-1β increased the release of sulfated glycosaminoglycans and hyaluronan from the explants into the culture media consistently with the decrease in uronic acid and collagen content in the cartilage explants. These catabolic effects were inhibited when cotreated with interleukin-1β and andrographolide. In primary equine chondrocytes, andrographolide suppressed interleukin-1β-induced MMP-2 mRNA expression and MMP-2 activity in the culture medium. These results confirmed the in vitro potent chondroprotective activities of this compound which were performed in cartilage explants and on a cellular level. These may indicate the application of andrographolide for therapeutic use in equine degenerative joint diseases.
机译:退行性关节疾病中的软骨侵蚀导致受影响马匹的me行。据报道,穿心莲中的穿心莲内酯抑制软骨基质降解酶。这项研究旨在探讨该化合物是否能保护外植体培养模型中的马软骨降解,并确定其对马软骨细胞培养物中基质金属蛋白酶2(MMP-2)表达(基质降解酶)的影响。在25 ng / mL穿心莲内酯或不含穿心莲内酯的培养物中,25 ng / mL白细胞介素-1β(软骨变性的关键诱导剂)诱导马关节软骨外植体培养。 3–21天后,对它们进行了软骨降解标记分析。发现白介素-1β增加了从外植体向培养基中的硫酸化糖胺聚糖和透明质酸的释放,与软骨外植体中糖醛酸和胶原含量的降低一致。与白介素-1β和穿心莲内酯共同治疗时,这些分解代谢作用受到抑制。在原代马软骨细胞中,穿心莲内酯可抑制白介素-1β诱导的培养基中MMP-2 mRNA表达和MMP-2活性。这些结果证实了该化合物在软骨外植体中和在细胞水平上进行的体外有效的软骨保护活性。这些可能表明穿心莲内酯在马变性关节疾病中的治疗用途。

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