首页> 外文期刊>Osteoarthritis and cartilage >Avocado soybean unsaponifiables (ASU) suppress TNF-alpha, IL-1beta, COX-2, iNOS gene expression, and prostaglandin E2 and nitric oxide production in articular chondrocytes and monocyte/macrophages.
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Avocado soybean unsaponifiables (ASU) suppress TNF-alpha, IL-1beta, COX-2, iNOS gene expression, and prostaglandin E2 and nitric oxide production in articular chondrocytes and monocyte/macrophages.

机译:鳄梨大豆不皂化物(ASU)抑制关节软骨细胞和单核细胞/巨噬细胞中的TNF-alpha,IL-1beta,COX-2,iNOS基因表达以及前列腺素E2和一氧化氮的产生。

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OBJECTIVE: To evaluate the effects of avocado soybean unsaponifiables (ASU) on proinflammatory mediators in chondrocytes and monocyte/macrophage-like cells. DESIGN: To determine the dose response of ASU, chondrocytes (5 x 10(5) cells/well) were incubated at 5% CO(2), 37 degrees C for 72 h with (1) control media alone or (2) ASU at concentrations of 0.3, 0.9, 2.7, 8.3, and 25 microg/ml. Cells were activated with 20 ng/ml lipopolysaccharide (LPS) for 24 h and cell supernatants were analyzed for prostaglandin E(2) (PGE(2)) and nitrite content. Chondrocytes and THP-1 monocyte/macrophages (5 x 10(5) cells/well) were incubated at 5% CO(2), 37 degrees C for 72 h with (1) control media alone or (2) ASU (25 mug/ml). One set of cells was activated for 1 h with LPS (20 ng/ml) for both reverse-transcriptase PCR and real-time PCR analysis of tumor necrosis factor-alpha (TNF-alpha), interleukin-1-beta (IL-1beta), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS) expression. One set of cells was activated for 24 h to analyze secreted PGE(2) and nitrite levels in the cellular supernatant. RESULTS: ASU reduced TNF-alpha, IL-1beta, COX-2, and iNOS expression in LPS-activated chondrocytes to levels similar to nonactivated control levels. The suppression of COX-2 and iNOS expression was paralleled by a significant reduction in PGE(2) and nitrite, respectively, in the cellular supernatant. ASU also reduced TNF-alpha and IL-1beta expression in LPS-activated monocyte/macrophage-like cells. CONCLUSION: The present study demonstrates that the anti-inflammatory activity of ASU is not restricted to chondrocytes, but also affects monocyte/macrophage-like cells that serve as a prototype for macrophages in the synovial membrane. These observations provide a scientific rationale for the pain-reducing and anti-inflammatory effects of ASU observed in osteoarthritis patients.
机译:目的:评价鳄梨大豆不皂化物(ASU)对软骨细胞和单核细胞/巨噬细胞样细胞促炎介质的影响。设计:为了确定ASU的剂量反应,将软骨细胞(5 x 10(5)个细胞/孔)在5%CO(2),37°C下与(1)单独的对照培养基或(2)ASU一起孵育72小时。浓度为0.3、0.9、2.7、8.3和25微克/毫升。用20 ng / ml脂多糖(LPS)激活细胞24小时,并分析细胞上清液中的前列腺素E(2)(PGE(2))和亚硝酸盐含量。软骨细胞和THP-1单核细胞/巨噬细胞(5 x 10(5)细胞/孔)在5%CO(2),37°C下与(1)单独的对照培养基或(2)ASU(25杯)一起孵育72小时/ ml)。用LPS(20 ng / ml)将一组细胞激活1小时,以进行逆转录酶PCR和实时PCR分析肿瘤坏死因子-α(TNF-alpha),白介素-1-β(IL-1beta) ),环氧合酶2(COX-2)和诱导型一氧化氮合酶(iNOS)的表达。激活一组细胞24小时,以分析细胞上清液中分泌的PGE(2)和亚硝酸盐水平。结果:ASU将LPS激活的软骨细胞中的TNF-α,IL-1beta,COX-2和iNOS表达降低到与未激活的对照水平相似的水平。 COX-2和iNOS表达的抑制与细胞上清液中PGE(2)和亚硝酸盐的显着降低同时发生。 ASU还可以降低LPS激活的单核细胞/巨噬细胞样细胞中TNF-α和IL-1beta的表达。结论:本研究表明,ASU的抗炎活性不仅限于软骨细胞,而且还影响滑膜膜中巨噬细胞原型的单核细胞/巨噬细胞样细胞。这些观察结果为在骨关节炎患者中观察到的ASU的减轻疼痛和抗炎作用提供了科学依据。

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