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Monounsaturated and Saturated but Not n-6 Polyunsaturated Fatty Acids Decrease Cartilage Destruction under Inflammatory Conditions

机译:单不饱和和饱和脂肪酸但不是n-6多不饱和脂肪酸可减少炎症条件下的软骨破坏

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摘要

Purpose: Osteoarthritis (OA) is associated with obesity in which altered fatty acid levels have been observed. We investigated whether the most common fatty acids in synovial fluid influence cartilage deterioration in OA. Design: Cartilage was obtained from OA patients undergoing total knee arthroplasty. Chondrocytes or cartilage explants were cultured with linoleic (n-6 polyunsaturated), oleic (monounsaturated), or palmitic (saturated) acid. After preculture, media were renewed and inflammation was simulated in half of the samples by addition of 10 ng/mL tumor necrosis factor-α (TNFα) with or without the fatty acids. Effects on lipid uptake (Oil-Red-O), cell toxicity (lactate dehydrogenase), prostaglandin-E2 (PGE2) release and gene expression for prostaglandin-endoperoxide synthase-2 (PTGS2), matrix metalloproteinase-1 (MMP1), and MMP13, and a disintegrin and metalloproteinase with thrombospondin motifs 4 were determined on chondrocytes in monolayer. Effects on glycosaminoglycan (GAG) release were evaluated on cartilage explants. Results: None of the fatty acids were cytotoxic and all were taken up by the cells, resulting in a higher amount of intracellular lipid in chondrocytes. Linoleic acid increased PGE2 production in the presence of TNFα. Oleic acid and palmitic acid inhibited MMP1 gene expression in chondrocytes stimulated with TNFα. In cartilage explants, GAG release was also inhibited by oleic acid and palmitic acid, and oleic acid decreased PTGS2 gene expression in stimulated chondrocytes. Conclusions: Linoleic acid has a pro-inflammatory effect on cartilage whereas oleic acid and palmitic acid seem to inhibit cartilage destruction. These results indicate that altered fatty acid levels may influence loss of cartilage structure in OA.
机译:目的:骨关节炎(OA)与肥胖有关,其中已观察到脂肪酸水平的改变。我们调查了滑液中最常见的脂肪酸是否影响OA中的软骨恶化。设计:软骨是从接受全膝关节置换术的OA患者获得的。用亚油酸(n-6多不饱和),油酸(单不饱和)或棕榈酸(饱和)培养软骨细胞或软骨外植体。预培养后,通过添加10 ng / mL含或不含脂肪酸的肿瘤坏死因子-α(TNFα),更新培养基并在一半样品中模拟炎症。对脂质摄取(Oil-Red-O),细胞毒性(乳酸脱氢酶),前列腺素E2(PGE2)释放和前列腺素内过氧化物合酶2(PTGS2),基质金属蛋白酶1(MMP1)和MMP13基因表达的影响,并在单层软骨细胞上测定了具有血小板反应蛋白基序4的Disintegrin和金属蛋白酶。在软骨外植体上评估了对糖胺聚糖(GAG)释放的影响。结果:没有一种脂肪酸具有细胞毒性,并且全部被细胞吸收,从而导致软骨细胞中的细胞内脂质含量更高。在TNFα存在下,亚油酸增加了PGE2的产生。油酸和棕榈酸抑制TNFα刺激的软骨细胞中MMP1基因表达。在软骨外植体中,油酸和棕榈酸也抑制了GAG的释放,油酸降低了刺激软骨细胞中PTGS2基因的表达。结论:亚油酸对软骨具有促炎作用,而油酸和棕榈酸似乎抑制软骨破坏。这些结果表明,改变脂肪酸水平可能会影响OA中软骨结构的丧失。

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