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天然成分来源的抗氧化剂通过 Keap1/Nrf2 通路减轻 HO 诱导的氧化应激,并对人骨性关节炎软骨细胞具有软骨保护作用。

Natural ingredients-derived antioxidants attenuate HO-induced oxidative stress and have chondroprotective effects on human osteoarthritic chondrocytes via Keap1/Nrf2 pathway.

机构信息

Center for Joint Surgery, Southwest Hospital, Army Medical University (Third Military Medical University), Chongqing, 400038, China.

Department of Orthopedics, Central Hospital of Chongqing University, Chongqing, 400014, China.

出版信息

Free Radic Biol Med. 2020 May 20;152:854-864. doi: 10.1016/j.freeradbiomed.2020.01.185. Epub 2020 Jan 31.

Abstract

Osteoarthritis (OA) is the most common disabling joint disease and its pathological process is closely related to oxidative stress. Recent studies have shown that antioxidants allicin, sulforaphane, and lycopene derived from natural ingredients garlic, broccoli, and tomato can reduce the degree of oxidative stress and the expression of inflammatory markers, indicating that theses antioxidants might be helpful for OA treatment. In this study, we investigated the effects of allicin, sulforaphane, and lycopene on HO-stimulated human osteochondral samples and osteoarthritic chondrocytes. Our results revealed that allicin, sulforaphane, and lycopene effectively reduced the oxidative stress-induced cell apoptosis, and increased gene expression of antioxidant enzymes. Besides, these natural ingredients-derived antioxidants reduced the expression of inflammatory factors, enhanced the chondrogenic matrix synthesis, and reduced the hypertrophic differentiation of osteoarthritic chondrocytes. These regulations were mainly through the activation of Keap1/Nrf2 pathway. Our findings suggest that these antioxidants might be a potential therapeutic strategy for OA.

摘要

骨关节炎(OA)是最常见的致残性关节疾病,其病理过程与氧化应激密切相关。最近的研究表明,天然成分大蒜中的抗氧化剂蒜素、西兰花中的萝卜硫素和番茄中的番茄红素,可以降低氧化应激程度和炎症标志物的表达,这表明这些抗氧化剂可能有助于 OA 的治疗。在这项研究中,我们研究了蒜素、萝卜硫素和番茄红素对 HO 刺激的人软骨样本和骨关节炎软骨细胞的影响。我们的结果表明,蒜素、萝卜硫素和番茄红素可有效降低氧化应激诱导的细胞凋亡,并增加抗氧化酶的基因表达。此外,这些天然成分衍生的抗氧化剂还可降低炎症因子的表达,增强软骨细胞的软骨基质合成,减少骨关节炎软骨细胞的肥大分化。这些调节作用主要是通过 Keap1/Nrf2 通路的激活来实现的。我们的研究结果表明,这些抗氧化剂可能是 OA 的一种潜在治疗策略。

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