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首页> 外文期刊>Osteoarthritis and cartilage >Inhibition of cyclooxygenase-2 expression and prostaglandin E2 production in chondrocytes by avocado soybean unsaponifiables and epigallocatechin gallate.
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Inhibition of cyclooxygenase-2 expression and prostaglandin E2 production in chondrocytes by avocado soybean unsaponifiables and epigallocatechin gallate.

机译:鳄梨大豆不皂化物和表没食子儿茶素没食子酸酯抑制软骨细胞中环氧合酶-2表达和前列腺素E2的产生。

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摘要

OBJECTIVE: To evaluate the anti-inflammatory effect of the combination of avocado soybean unsaponifiables (ASU) and epigallocatechin gallate (EGCG) on cyclooxygenase-2 (COX-2) expression and prostaglandin E(2) (PGE(2)) production in cytokine-activated equine chondrocytes. METHODS: Production of type II collagen and aggrecan was verified by immunohistochemistry and Western blot. Chondrocytes were incubated with: (1) control media alone, (2) ASU (4 microg/ml; 8.3 microg/ml), (3) EGCG (4, 40, 400 ng/ml), or (4) the combination of ASU and EGCG for 24h. Cells were next incubated with control medium alone or with IL-1beta (10 ng/ml) and TNF-alpha (1 ng/ml). COX-2 gene expression by real-time PCR analysis and NF-kappaB nuclear translocation by immunohistochemistry were performed after 1h of incubation. PGE(2) production was determined by immunoassay after 24h of incubation. RESULTS: Equine chondrocytes responded to cytokine activation by up-regulated gene expression of COX-2 and increased PGE(2) production. Activation was associated with NF-kappaB translocation. Individually, ASU and EGCG marginally inhibited COX-2 expression and PGE(2) production in activated chondrocytes. In contrast, the combination of ASU and EGCG reduced COX-2 expression close to non-activated control levels and significantly inhibited PGE(2) production. These reductions were statistically greater than those of ASU or EGCG alone. The inhibition of COX-2 expression and PGE(2) production was associated with inhibition of NF-kappaB translocation. CONCLUSION: The present study demonstrates that the anti-inflammatory activity of ASU and EGCG is potentiated when used in combination. This combination may offer an attractive supplement or alternative to non-steroidal anti-inflammatory drugs (NSAIDs) in the management of osteoarthritis.
机译:目的:评估鳄梨大豆不皂化物(ASU)和表没食子儿茶素没食子酸酯(EGCG)组合对细胞因子中环氧合酶2(COX-2)表达和前列腺素E(2)(PGE(2))产生的抗炎作用。激活的马软骨细胞。方法:通过免疫组织化学和Western blot验证II型胶原蛋白和聚集蛋白聚糖的产生。将软骨细胞与(1)单独的对照培养基,(2)ASU(4 microg / ml; 8.3 microg / ml),(3)EGCG(4、40、400 ng / ml)或(4) ASU和EGCG持续24小时。接下来,将细胞与单独的对照培养基或与IL-1beta(10 ng / ml)和TNF-alpha(1 ng / ml)一起孵育。孵育1小时后,通过实时PCR分析进行COX-2基因表达,并通过免疫组织化学进行NF-κB核易位。孵育24小时后,通过免疫测定法确定PGE(2)的产生。结果:马软骨细胞通过上调COX-2的基因表达和增加PGE(2)的产生来响应细胞因子的激活。激活与NF-κB易位有关。单独地,ASU和EGCG在激活的软骨细胞中略微抑制COX-2表达和PGE(2)的产生。相比之下,ASU和EGCG的组合降低了COX-2的表达,接近未激活的对照水平,并显着抑制了PGE(2)的产生。从统计上看,这些减少量大于单独使用ASU或EGCG的减少量。抑制COX-2表达和PGE(2)的生产与抑制NF-κB易位有关。结论:本研究表明,当联合使用时,ASU和EGCG的抗炎活性增强。这种组合可以在骨关节炎的治疗中提供非甾体抗炎药(NSAIDs)的有吸引力的补充剂或替代品。

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