Au R Y, Al-Talib T K, Au A Y, Phan P V, Frondoza C G
Nutramax Laboratories, Inc., Edgewood, MD 21040, USA.
Osteoarthritis Cartilage. 2007 Nov;15(11):1249-55. doi: 10.1016/j.joca.2007.07.009. Epub 2007 Sep 12.
To evaluate the effects of avocado soybean unsaponifiables (ASU) on proinflammatory mediators in chondrocytes and monocyte/macrophage-like cells.
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.
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.
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.
评估鳄梨大豆不皂化物(ASU)对软骨细胞和单核细胞/巨噬细胞样细胞中促炎介质的影响。
为确定ASU的剂量反应,将软骨细胞(5×10⁵个细胞/孔)在5%二氧化碳、37℃条件下培养72小时,培养条件为:(1)仅用对照培养基;(2)分别用浓度为0.3、0.9、2.7、8.3和25微克/毫升的ASU。用20纳克/毫升脂多糖(LPS)激活细胞24小时,分析细胞上清液中前列腺素E₂(PGE₂)和亚硝酸盐含量。将软骨细胞和THP-1单核细胞/巨噬细胞(5×10⁵个细胞/孔)在5%二氧化碳、37℃条件下培养72小时,培养条件为:(1)仅用对照培养基;(2)ASU(25微克/毫升)。一组细胞用LPS(20纳克/毫升)激活1小时,用于逆转录聚合酶链反应(RT-PCR)和实时聚合酶链反应(real-time PCR)分析肿瘤坏死因子-α(TNF-α)、白细胞介素-1-β(IL-1β)、环氧化酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)的表达。另一组细胞激活24小时,分析细胞上清液中分泌的PGE₂和亚硝酸盐水平。
ASU将LPS激活的软骨细胞中TNF-α、IL-1β、COX-2和iNOS的表达降低至与未激活的对照水平相似。COX-2和iNOS表达的抑制分别伴随着细胞上清液中PGE₂和亚硝酸盐的显著降低。ASU还降低了LPS激活的单核细胞/巨噬细胞样细胞中TNF-α和IL-1β的表达。
本研究表明,ASU的抗炎活性不仅限于软骨细胞,还影响作为滑膜巨噬细胞原型的单核细胞/巨噬细胞样细胞。这些观察结果为骨关节炎患者中观察到的ASU的止痛和抗炎作用提供了科学依据。