Nutramax Laboratories Inc, Edgewood, MD 21040, USA.
Evid Based Complement Alternat Med. 2008 Jun;5(2):191-7. doi: 10.1093/ecam/nem132.
Avocado/soy unsaponifiable (ASU) components are reported to have a chondroprotective effect by virtue of anti-inflammatory and proanabolic effects on articular chondrocytes. The identity of the active component(s) remains unknown. In general, sterols, the major component of unsaponifiable plant material have been demonstrated to be anti-inflammatory in vitro and in animal models. These studies were designed to clarify whether the sterol content of ASU preparations were the primary contributors to biological activity in articular chondrocytes. ASU samples were analyzed by high pressure liquid chromatography (HPLC) and GC mass spectrometry. The sterol content was normalized between diverse samples prior to in vitro testing on bovine chondrocytes. Anabolic activity was monitored by uptake of 35-sulfate into proteoglycans and quantitation of labeled hydroxyproline and proline content after incubation with labeled proline. Anti-inflammatory activity was assayed by measuring reduction of interleukin-1 (IL-1)-induced synthesis of PGE2 and metalloproteases and release of label from tissue prelabeled with S-35.All ASU samples exerted a similar time-dependent up-regulation of 35-sulfate uptake in bovine cells reaching a maximum of greater than 100% after 72 h at sterol doses of 1-10 mug/ml. Non-collagenous protein (NCP) and collagen synthesis were similarly up-regulated. All ASU were equally effective in dose dependently inhibiting IL-1-induced MMP-3 activity (23-37%), labeled sulfate release (15-23%) and PGE2 synthesis (45-58%). Up-regulation of glycosaminoglycan and collagen synthesis and reduction of IL-1 effects in cartilage are consistent with chondroprotective activity. The similarity of activity of ASU from diverse sources when tested at equal sterol levels suggests sterols are important for biologic effects in articular chondrocytes.
鳄梨/大豆不可皂化物(ASU)成分被报道具有软骨保护作用,这是由于其对关节软骨细胞具有抗炎和促进合成代谢的作用。其活性成分的身份仍不清楚。一般来说,甾醇是不可皂化物植物材料的主要成分,已被证明具有体外和动物模型中的抗炎作用。这些研究旨在阐明 ASU 制剂中的甾醇含量是否是关节软骨细胞中生物活性的主要贡献者。通过高压液相色谱(HPLC)和 GC 质谱对 ASU 样品进行分析。在进行体外牛软骨细胞试验之前,对不同样品中的甾醇含量进行归一化。通过 35-硫酸盐摄取到蛋白聚糖中以及孵育标记脯氨酸后标记羟脯氨酸和脯氨酸含量的定量来监测合成代谢活性。通过测量白细胞介素-1(IL-1)诱导的 PGE2 和金属蛋白酶合成以及从预先用 S-35 标记的组织中释放标记物来测定抗炎活性。所有 ASU 样品均在牛细胞中表现出相似的时间依赖性 35-硫酸盐摄取上调,在固醇剂量为 1-10 μg/ml 时,72 小时后达到最大上调超过 100%。非胶原蛋白(NCP)和胶原蛋白合成也被上调。所有 ASU 均以剂量依赖性方式有效抑制 IL-1 诱导的 MMP-3 活性(23-37%),标记硫酸盐释放(15-23%)和 PGE2 合成(45-58%)。糖胺聚糖和胶原蛋白合成的上调以及软骨中 IL-1 作用的减少与软骨保护活性一致。当以相等的甾醇水平测试来自不同来源的 ASU 时,活性的相似性表明甾醇对关节软骨细胞的生物学效应很重要。