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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Effect of Angelica sinensis Polysaccharides on Osteoarthritis In Vivo and In Vitro: A Possible Mechanism to Promote Proteoglycans Synthesis
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Effect of Angelica sinensis Polysaccharides on Osteoarthritis In Vivo and In Vitro: A Possible Mechanism to Promote Proteoglycans Synthesis

机译:当归多糖对骨关节炎的体内和体外影响:促进蛋白聚糖合成的可能机制。

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摘要

This study investigated the effect of Angelica sinensis polysaccharides (APS-3c) on rat osteoarthritis (OA) model in vivo and rat interleukin-1-beta- (IL-1beta-) stimulated chondrocytes in vitro. APS-3c was administrated into rat OA knee joints and had protective effects on rat OA cartilage in vivo. Primary rat articular chondrocytes were cotreated with APS-3c and IL-1beta in vitro. 2~50 mug/mL APS-3c had no effect on chondrocytes viability, whereas it increased the proteoglycans (PGs) synthesis inhibited by IL-1beta. Microarray analysis showed that the significant changes were concentrated in the genes which were involved in PGs synthesis. RT-PCR confirmed that treatment with APS-3c increased the mRNA expression of aggrecan and glycosyltransferases (GTs) inhibited by IL-1beta but did not affect the mRNA expression of matrix-degrading enzymes. These results indicate that APS-3c can improve PGs synthesis of chondrocytes on rat OA model in vivo and IL-lbeta-stimulated chondrocytes in vitro, which is due to the promotion of the expression of aggrecan and GTs involved in PGs synthesis but not the inhibition of the expression of matrix-degrading enzymes. Our findings suggest the clinical relevance of APS-3c in the prospective of future alternative medical treatment for OA.
机译:这项研究调查了当归多糖(APS-3c)对大鼠骨关节炎(OA)模型体内和大鼠白介素-1-β(IL-1beta-)刺激的软骨细胞的影响。 APS-3c被施用于大鼠OA膝关节,并在体内对大鼠OA软骨具有保护作用。大鼠原代软骨细胞在体外用APS-3c和IL-1beta共同处理。 2〜50马克杯/毫升的APS-3c对软骨细胞的存活率没有影响,而增加了IL-1β抑制的蛋白聚糖(PGs)的合成。芯片分析表明,显着的变化集中在与PGs合成有关的基因中。 RT-PCR证实,用APS-3c处理可增加被IL-1beta抑制的聚集蛋白聚糖和糖基转移酶(GTs)的mRNA表达,但不影响基质降解酶的mRNA表达。这些结果表明,APS-3c可以改善大鼠OA模型体内软骨细胞的PGs合成和体外IL-1β刺激的软骨细胞的PGs合成,这是由于促进了聚集蛋白聚糖和GTs的表达而参与了PGs的合成,但没有抑制作用基质降解酶的表达我们的研究结果表明APS-3c在OA的替代治疗方面具有临床意义。

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