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Enzymes associated with anti-inflammatory potentialities of purified terpenoid extracts from the selected sea weeds

机译:来自选定的海杂草纯化的萜烯蛋白提取物的抗炎潜力相关的酶

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Introduction: Macrophages are phagocytic WBCs involved in the immune defense and will be activated during inflammatory disorders.?The synthesis of cytokines and mediators, particularly nitric oxide (NO) is triggered by the macrophage activator. NO induces many biological events.?Therefore, NO regulation is proven to be potential for exploring anti-inflammatory drugs. Aim: The anti-inflammatory action of the purified terpenoid extracts from red algae such as Hypnea musciformis, Gracilaria dura and Kappaphycus alvarezii on LPS induced RAW 264.7 macrophages on lipoxygenase, cyclooxygenase, hyaluronidase, xanthine oxidase and myeloperoxidase inhibitory effects were evaluated. Methods: The methanolic extract of the sea weeds were subjected to silica gel column chromatography and the fraction was further subjected to GC-MS analysis. Then, the potentiality of the purified terpenoid extracts to inhibit various inflammation causing enzymes such as COX, LOX, hyaluronidase, xanthineoxidase and myeloperoxidase were carried out. Findings: The terpenoid extracts reduced the enzyme activities in a dose dependent manner as compared to control group.?The extracts inhibited xanthine oxidase activity effectively at 250 μg/ml i.e., a maximum inhibitory activity of 62.1% as compared to the standard drug, allopurinol. The extract significantly inhibited lipoxygenase activity, with highest inhibitory activity at 100 μg/ml. The nitric acid synthesis was reduced to 8.5 μM by Hypnea musciformis. Conclusion: The present study revealed that the purified terpenoid extracts from H. musciformis exhibited potent anti-inflammatory activities followed by G. dura and K. alvarezii via regulating the anti-inflammatory enzymes. These findings provide justification for the traditional use of?the red algae in inflammatory conditions.
机译:介绍:巨噬细胞是吞噬免疫防御的吞噬WBC,并在炎症紊乱期间激活。细胞因子和介质的合成,特别是巨噬细胞活化剂引发的细胞因子和介质,特别是一氧化氮(NO)。没有诱导许多生物事件。因此,没有被证明没有监管是探索抗炎药的潜力。目的:评估RPS的红藻(RPEA Musciformis),Gracilaria Dura和Kappaphycus Alvarezii对LPS的抗炎脂肪蛋白提取物的抗炎作用诱导原料264.7巨噬细胞对脂氧合酶,环氧氧酶,透明质酸酶,黄嘌呤氧化酶和髓氧化酶抑制作用。方法:海杂草的甲醇提取物对硅胶柱色谱法进行硅胶柱色谱,进一步进行GC-MS分析。然后,进行纯化的萜类醇提取物的潜在能力,以抑制导致酶如COX,LOX,透明质酸酶,黄嘌呤氧化酶和髓氧化酶等酶的各种炎症。结果:与对照组相比,萜类化提取物以剂量依赖性方式减少了酶活性。当量抑制黄嘌呤氧化酶活性,在250μg/ ml,即与标准药物,alopurinol相比,最大抑制活性为62.1% 。提取物显着抑制脂氧合酶活性,在100μg/ ml下具有最高的抑制活性。通过Hypnea Musciformis将硝酸合成降至8.5μm。结论:本研究表明,来自H.Musciformis的纯化的萜类蛋白提取物表现出效力的抗炎活动,然后通过调节抗炎酶来表现出G.Dura和K.Alvarezii。这些发现提供了传统使用的理由?炎症条件下的红藻。

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