罗氏链霉菌OF1产胞外多糖及其通过抑制TNF-α/COX2途径改善大鼠骨关节炎的作用研究。

IF 3.6 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Sahar Saleh Mohamed, Mohamed E El Awady, Sayeda Abdelrazek Abdelhamid, Ahmed Abdelghani Hamed, Abeer A A Salama, Manal S Selim
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引用次数: 3

摘要

背景:碳水化合物是生命活动的主要天然产物。结果:红树罗氏链霉菌OF1分离得到的胞外多糖S5 (EPSS5) (14.2 gl-1)含硫酸脲酸21.98%,含量11.65 mg/ml,黏度1.35 mm2/s。总己糖胺含量为24.72%。单糖的高效液相色谱分析表明,EPS由麦芽糖酸、葡萄糖醛酸、木糖和果糖组成,摩尔比分别为1.0:0.5:1.0:2.0。结果表明,总抗氧化活性为92.06%。对金黄色葡萄球菌、大肠杆菌、耐甲氧西林金黄色葡萄球菌和肺炎克雷伯菌均有抑菌活性。但EPSS5对白色念珠菌的抗真菌活性较低。而对黑曲霉没有检测到抗真菌活性。EPSS5对金黄色葡萄球菌具有明显的抗生物膜作用,对生物膜的抑制率高达50%。EPS对血清TNF-α和COX2水平的影响分别为2倍和1.9倍,使血清肿瘤坏死因子-α (TNF-α)水平分别降低38%、12%、49%,环氧化酶-2 (COX2)水平分别降低61%、34%和62%。EPSS5对卡拉胶刺激大鼠关节炎的影响。结论:EPS可改善卡拉胶诱导的炎症介质升高;与卡拉胶组相比,TNF-α/COX和金属蛋白酶9 (MMP9)的表达分别降低68%、86%和75%。再一次,与游离药物相比,高剂量的治疗只降低了57%的MMP9水平,这表明EPSS5是一种很好的MMP9抑制剂,因为它通过信号通路使MMP9恢复到正常水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Study of exopolysaccharide produced by Streptomyces rochie strain OF1 and its effect as ameliorative on osteoarthritis in rats via inhibiting TNF-α/COX2 pathway.

Study of exopolysaccharide produced by Streptomyces rochie strain OF1 and its effect as ameliorative on osteoarthritis in rats via inhibiting TNF-α/COX2 pathway.

Study of exopolysaccharide produced by Streptomyces rochie strain OF1 and its effect as ameliorative on osteoarthritis in rats via inhibiting TNF-α/COX2 pathway.

Study of exopolysaccharide produced by Streptomyces rochie strain OF1 and its effect as ameliorative on osteoarthritis in rats via inhibiting TNF-α/COX2 pathway.

Background: Carbohydrates are known as the main natural products of life activities.

Results: Streptomyces rochie strain OF1 isolated from a mangrove tree produced exopolysaccharide S5 (EPSS5) (14.2 gl-1) containing uronic acid 21.98% sulfate content of 11.65 mg/ml, and a viscosity of 1.35 mm2/s. while total hexose amine content was 24.72%. The high performance liquid chromatography (HPLC) analysis of mono sugars revealed that EPS was composed of manouronic acid, glucuronic acid, xylose, and fructose at a molar ratio of 1.0:0.5:1.0:2.0, respectively. It showed that the whole antioxidant activity was 92.06%. It showed antibacterial activity against Staphylococcus aureus, and E. coli, MRSA and Klebsiella pneumoniae. But, EPSS5 displayed low antifungal activity against Candida albicans. While no antifungal activity has been detected against Aspergillus niger. EPSS5 has antibiofilm action that is noticeable toward S. aureus with an inhibition ratio of biofilm up to 50%. Effect of EPS on serum levels of TNF-α and COX2 by 2 fold and 1.9 fold of EPS reduced serum levels of Tumor necrosis factor-α (TNF-α) by 38%, 12%, 49%, and Cyclooxygenase-2 (COX2) by 61%, 34%, and 62%, respectively. By affected of EPSS5 on arthritis in rats stimulated by carrageenan.

Conclusions: Administration of EPS ameliorated carrageen-induced elevation in inflammatory mediators; TNF-α/COX and suppressed the expressions of metalloproteinase 9 (MMP9) by 68%, 86%, and 75% correspondingly in comparison to the group of carrageenans. Then again, therapy involving a high dose only reduced MMP9 level by 57%, compared to free drug suggesting that EPSS5 is a good inhibitor of the MMP9, as it brought MMP9 back to normal levels via the signaling pathway.

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