Yuan Li, Chu Qian, Wu Xiaoyun, Yang Bei, Zhang Wei, Jin Wengang, Gao Ruichang
School of Food and Biological Engineering, Jiangsu University, Zhenjiang, China.
Bio-Resources Key Laboratory of Shaanxi Province, School of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, China.
Front Nutr. 2021 Jun 11;8:689648. doi: 10.3389/fnut.2021.689648. eCollection 2021.
Research has shown that cartilage containing chondroitin sulfate and protein presents versatile bioactivities. Chondroitin sulfate in cartilage is beneficial to activate the immune system while the protein/peptide has not been fully understood. The current study investigated the antioxidant and anti-inflammatory properties of ethanol-soluble hydrolysates of sturgeon cartilage (ESCH) prepared through hot-pressure, enzymatic hydrolysis and ethanol extraction. UV spectrum, IR and agarose gel electrophoresis results suggested the successful exclusion of chondroitin sulfate from peptides. Nitric oxide (NO) floods in cells activated by inflammation. It was inhibited when administrated with ESCH. To further explain the observed anti-inflammatory activity, ESCH was separated with Sephadex G-15 into 3 components, among which F3 showed a higher NO inhibition rate and significantly reduced the production of the proinflammatory cytokine IL-6. In addition, the yield of IL-10 increased. Western blotting suggested that F3 downregulated the NO content and IL-6 level by suppressing Mitogen-activated protein kinases (MAPK) channels. Moreover, both ESCH and F3 showed DPPH and ABTS free radical scavenging abilities which was possibly related to the anti-inflammatory property. These results indicated that ESCH behaved anti-inflammatory and antioxidant activities. Cartilage may be a good source to produce anti-inflammatory peptides.
研究表明,含有硫酸软骨素和蛋白质的软骨具有多种生物活性。软骨中的硫酸软骨素有利于激活免疫系统,而蛋白质/肽的作用尚未完全明确。本研究调查了通过热压、酶解和乙醇萃取制备的鲟鱼软骨乙醇溶性水解物(ESCH)的抗氧化和抗炎特性。紫外光谱、红外光谱和琼脂糖凝胶电泳结果表明,肽中成功排除了硫酸软骨素。炎症激活的细胞中会大量产生一氧化氮(NO)。给予ESCH后,NO的产生受到抑制。为进一步解释观察到的抗炎活性,用葡聚糖凝胶G-15将ESCH分离为3个组分,其中F3显示出较高的NO抑制率,并显著降低促炎细胞因子IL-6的产生。此外,IL-10的产量增加。蛋白质印迹法表明,F3通过抑制丝裂原活化蛋白激酶(MAPK)通道下调NO含量和IL-6水平。此外,ESCH和F3均表现出DPPH和ABTS自由基清除能力,这可能与抗炎特性有关。这些结果表明,ESCH具有抗炎和抗氧化活性。软骨可能是生产抗炎肽的良好来源。