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Chamazulene reverses osteoarthritic inflammation through regulation of matrix metalloproteinases (MMPs) and NF-kβ pathway in in-vitro and in-vivo models.
Bioscience, Biotechnology, and Biochemistry ( IF 1.6 ) Pub Date : 2019-10-23 , DOI: 10.1080/09168451.2019.1682511
Ding Ma 1 , Jinlong He 2 , Dapeng He 3
Affiliation  

This study was conducted to evaluate the protective effects of chamazulene against IL-1β-induced rat primary chondrocytes and complete Freund's adjuvant (CFA)-induced osteoarthritic inflammation in rats. Oxidative stress markers, pro-inflammatory cytokines, and regulatory proteins were measured. Chamazulene significantly reverted (p < 0.05) the levels of lipid peroxidation and enhanced the activities of superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT) enzymes against IL-1β and CFA-induced oxidative stress. The levels of TNF-α and IL-6 were reduced (p < 0.05) in chamazulene treatment against IL-1β and CFA-induced inflammation. Western blot analysis results on the expressions of MMP-3, MMP-9, p65 NF-kβ, iNOS, and COX-2 showed chamazulene was able to protect the chondrocytes against IL-1β-induced osteoarthritic inflammation. Histopathology of rat hind ankle showed chamazulene significantly protected against CFA-induced osteoarthritic inflammation. Therefore, chamazulene can be recommended as a therapeutic agent for clinical trials against osteoarthritic inflammation.

中文翻译:

在体外和体内模型中,Chamazulene通过调节基质金属蛋白酶(MMP)和NF-kβ途径逆转骨关节炎炎症。

进行了这项研究,以评估甲磺灵对IL-1β诱导的大鼠原代软骨细胞和完全弗氏佐剂(CFA)诱导的大鼠骨关节炎的保护作用。测量了氧化应激标志物,促炎细胞因子和调节蛋白。Chamazulene显着还原(p <0.05)脂质过氧化水平,并增强了针对IL-1β和CFA诱导的氧化应激的超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)酶的活性。在Chamazulene对抗IL-1β和CFA诱导的炎症的治疗中,TNF-α和IL-6的水平降低(p <0.05)。蛋白质印迹分析结果显示MMP-3,MMP-9,p65NF-kβ,iNOS,COX-2的结果表明chamazulene能够保护软骨细胞免受IL-1β诱导的骨关节炎的炎症。大鼠后踝的组织病理学研究显示,马甲富烯对CFA诱导的骨关节炎炎症具有明显的保护作用。因此,可以推荐使用马甲磺胺作为抗骨关节炎炎症的临床试验的治疗剂。
更新日期:2019-12-19
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