首页> 美国卫生研究院文献>Journal of Ginseng Research >Protective Effect of Ginsenoside Rb1 on Hydrogen Peroxide-induced Oxidative Stress in Rat Articular Chondrocytes
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Protective Effect of Ginsenoside Rb1 on Hydrogen Peroxide-induced Oxidative Stress in Rat Articular Chondrocytes

机译:人参皂苷Rb1对过氧化氢诱导的大鼠软骨细胞氧化应激的保护作用。

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摘要

The abnormal maturation and ossification of articular chondrocytes play a central role in the pathogenesis of osteoarthritis (OA). Inhibiting the enzymatic degradation of the extracellular matrix and maintaining the cellular phenotype are two of the major goals of interest in managing OA. Ginseng is frequently taken orally, as a crude substance, as a traditional medicine in Asian countries. Ginsenoside Rb1, a major component of ginseng that contains an aglycone with a dammarane skeleton, has been reported to exhibit various biological activities, including anti-inflammatory and anti-tumor effects. However, a chondroprotective effect of ginsenoside Rb1 related to OA has not yet been reported. The purpose of this study was to demonstrate the chondroprotective effect of ginsenoside Rb1 on the regulation of pro-inflammatory factors and chondrogenic genes. Cultured rat articular chondrocytes were treated with 100 μM ginsenoside Rb1 and/or 500 μM hydrogen peroxide (H2O2) and assessed for viability, reactive oxygen species production, nitric oxide (NO) release, and chondrogenic gene expression. Ginsenoside Rb1 treatment resulted in reductions in the levels of pro-inflammatory cytokine and NO in H2O2-treated chondrocytes. The expression levels of chondrogenic genes, such as type II collagen and SOX9, were increased in the presence of ginsenoside Rb1, whereas the expression levels of inflammatory genes related to chondrocytes, such as MMP1 and MMP13, were reduced by approximately 50%. These results suggest that ginsenoside Rb1 has potential for use as a therapeutic agent in OA patients.
机译:关节软骨细胞的异常成熟和骨化在骨关节炎(OA)的发病机理中起着核心作用。抑制细胞外基质的酶促降解并维持细胞表型是管理OA的两个主要目标。在亚洲国家,人参常作为原料药经口服服用。人参皂苷Rb1是人参的主要成分,它含有具有dammarane骨架的糖苷配基,据报道具有多种生物活性,包括抗炎和抗肿瘤作用。但是,尚未报道与OA有关的人参皂苷Rb1的软骨保护作用。这项研究的目的是证明人参皂苷Rb1对促炎因子和软骨形成基因的调节具有软骨保护作用。用100μM人参皂甙Rb1和/或500μM过氧化氢(H2O2)处理培养的大鼠关节软骨细胞,并评估其生存力,活性氧的产生,一氧化氮(NO)的释放和软骨形成基因的表达。人参皂甙Rb1处理导致H2O2处理的软骨细胞中促炎性细胞因子和NO水平降低。在人参皂苷Rb1存在的情况下,软骨生成基因(如II型胶原蛋白和SOX9)的表达水平增加,而与软骨细胞相关的炎症基因(如MMP1和MMP13)的表达水平降低了约50%。这些结果表明人参皂苷Rb1有潜力用作OA患者的治疗剂。

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