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首页> 外文期刊>Osteoarthritis and cartilage >Glucosamine decreases expression of anabolic and catabolic genes in human osteoarthritic cartilage explants.
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Glucosamine decreases expression of anabolic and catabolic genes in human osteoarthritic cartilage explants.

机译:葡萄糖胺降低人骨关节炎软骨外植体中合成代谢和分解代谢基因的表达。

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OBJECTIVE: To investigate the effect of glucosamine (GlcN) in a human osteoarthritic explant model on expression of genes involved in anabolic and catabolic activities of chondrocytes. METHODS: Human osteoarthritic explants, obtained during knee arthroplasty surgery, were pre-cultured (3 days) and treated with glucosamine-hydrochloride (GlcN-HCl) or glucosamine-3-sulphate (GlcN-S) at 0.5mM and 5mM (4 days). RNA was isolated from the explants and real time RT-PCR was performed. Additionally, total matrix metalloproteinase (MMP) activity was measured in culture medium. RESULTS: Addition of 5mM GlcN led to significant down-regulation of aggrecan (2.65-7.73-fold) and collagen type II (7.75-22.17-fold) gene expression, indicating inhibited anabolic activity. Considering catabolic activities, 5mM GlcN significantly down-regulated aggrecanase-1 and MMP3 and 5mM GlcN-S additionally down-regulated aggrecanase-2 and tissue inhibitor of MMP gene expression significantly. Gene expression was not significantly altered by 0.5mM GlcN. Total MMP activity in culture medium was only significantly reduced after addition of 5mM GlcN-HCl. CONCLUSION: The effects of GlcN on gene expression in a human osteoarthritic explant model suggest that enzymatic breakdown of the extra-cellular matrix might be reduced by the addition of 5mM GlcN. Additionally, restoration of already damaged cartilage is not to be expected, because gene expression of anabolic genes is also down-regulated. We suggest that chondroprotective properties of GlcN in vivo may be based on inhibiting further degradation due to catabolic activities, rather than on the ability to rebuild cartilage.
机译:目的:探讨葡萄糖胺(GlcN)在人骨关节炎外植体模型中对软骨细胞合成代谢和分解代谢相关基因表达的影响。方法:将在膝关节置换术中获得的人骨关节炎外植体进行预培养(3天),并分别在0.5mM和5mM(4天)中用盐酸氨基葡萄糖(GlcN-HCl)或氨基葡萄糖-3-硫酸盐(GlcN-S)处理。 )。从外植体中分离RNA,并进行实时RT-PCR。另外,在培养基中测量总基质金属蛋白酶(MMP)活性。结果:添加5mM GlcN导致聚集蛋白聚糖(2.65-7.73倍)和II型胶原(7.75-22.17倍)基因表达的显着下调,表明合成代谢活性受到抑制。考虑到分解代谢活性,5mM GlcN显着下调了agrecanase-1和MMP3,5mM GlcN-S额外下调了agrecanase-2和MMP基因表达的组织抑制剂。 0.5mM GlcN不会显着改变基因表达。加入5mM GlcN-HCl后,培养基中的总MMP活性仅显着降低。结论:GlcN对人骨关节炎外植体模型基因表达的影响表明,添加5mM GlcN可以减少细胞外基质的酶促降解。另外,由于合成代谢基因的基因表达也被下调,因此不希望恢复已经受损的软骨。我们建议,在体内GlcN的软骨保护特性可能是基于抑制由于分解代谢活动引起的进一步降解,而不是基于重建软骨的能力。

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