首页> 美国卫生研究院文献>Journal of Ginseng Research >Anti-apoptotic Activity of Ginsenoside Rb1 in Hydrogen Peroxide-treated Chondrocytes: Stabilization of Mitochondria and the Inhibition of Caspase-3
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Anti-apoptotic Activity of Ginsenoside Rb1 in Hydrogen Peroxide-treated Chondrocytes: Stabilization of Mitochondria and the Inhibition of Caspase-3

机译:人参皂苷Rb1在过氧化氢处理的软骨细胞中的抗凋亡活性:线粒体的稳定和Caspase-3的抑制作用。

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摘要

Chondrocyte apoptosis has been recognized as an important factor in the pathogenesis of osteoarthritis (OA). Hydrogen peroxide (H2O2), which produces reactive oxygen species, reportedly induces apoptosis in chondrocytes. The ginsenoside Rb1 (GRb1) is the principal component in ginseng and has been shown to have a variety of biological activities, such as anti-arthritis, anti-inflammation, and anti-tumor activities. In this study, we evaluated the effects of G-Rb1 on the mitochondrial permeability transition (MPT) and caspase-3 activity of chondrocyte apoptosis induced by H2O2. Cultured rat articular chondrocytes were exposed to H2O2 with or without G-Rb1 and assessed for viability, MPT, Bcl-xL/Bax expression, caspase-3 activity, and apoptosis. The co-treatment with G-Rb1 showed an inhibition of MPT, caspase-3 activity, and cell death. Additionally, the levels of the apoptotic protein Bax were significantly lower and the levels of the anti-apoptotic protein Bcl-xL were higher compared with H2O2 treatment alone. The results of this study demonstrate that G-Rb1 protects chondrocytes against H2O2-induced apoptosis, at least in part via the inhibition of MPT and caspase-3 activity. These results demonstrate that G-Rb1 is a potentially useful drug for the treatment of OA patients.
机译:软骨细胞凋亡已被认为是骨关节炎(OA)发病机理中的重要因素。据报道,产生活性氧的过氧化氢(H2O2)诱导软骨细胞凋亡。人参皂甙Rb1(GRb1)是人参中的主要成分,已被证明具有多种生物活性,例如抗关节炎,抗发炎和抗肿瘤活性。在这项研究中,我们评估了G-Rb1对H2O2诱导的软骨细胞凋亡的线粒体通透性转变(MPT)和caspase-3活性的影响。将培养的大鼠关节软骨细胞暴露于有或没有G-Rb1的H2O2中,并评估其活力,MPT,Bcl-xL / Bax表达,caspase-3活性和凋亡。与G-Rb1的共同治疗显示出对MPT,caspase-3活性和细胞死亡的抑制作用。另外,与单独的H 2 O 2处理相比,凋亡蛋白Bax的水平显着较低,而抗凋亡蛋白Bcl-xL的水平较高。这项研究的结果表明,G-Rb1至少部分通过抑制MPT和caspase-3活性来保护软骨细胞免受H2O2诱导的凋亡。这些结果表明,G-Rb 1 是治疗OA患者的潜在有用药物。

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