Aktivitas Antiinflamasi Crude Extract Fukoidan dari Sargassum crassifolium pada Sel RAW 264.7 yang Diinduksi LPS

Pangartika Hikariastri, Hendig Winarno, Kusmardi Kusmardi, Dian Ratih Laksmitawati, Syamsudin Abdillah
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引用次数: 2

Abstract

Inflammation is known as the basic mechanism underlying various chronic diseases. Macrophage activation by inflammatory stimulus induces the release of inflammatory mediators, thus the mediators becoming a promising target of anti-inflammatory drug development. Previous studies indicated that fucoidan has anti-inflammatory activity by inhibiting the release of proinflammatory mediators. The aim of this study is determining anti-inflammatory activity of fucoidan crude extract form Sargassum crassifolium Garut waters by observing its effect on proinflammatory cytokines TNF-α, IL-1β, dan IL-6. Fucoidan is a polysaccharide substance which has various characteristics, depending on the source and the extraction method which is influencing its bioactivity. Sargassum crassifolium collected from Garut-West Java is extracted using diluted HCl 0,1 M and precipitated with ethanol to obtain fucoidan crude extract. The crude extract is tested on LPS-induced RAW 264.7 cells to evaluate its effect on TNF-α, IL-1β, and IL-6 level using ELISA method. The result showed that fucoidan crude extract decreased the level of TNF-α by the dose of 25 and 50 μg/ml, and decreased the level of IL-1β and IL-6 by the dose of 25 μg/ml. The dose of 50 μg/ml failed to inhibit IL-1β and IL-6 production. This study showed that fucoidan crude extract derived from S. crassifolium has anti-inflammatory activity to RAW 264.7 cells by the dose of 25 μg/ml.
厚叶马尾藻粗提物对LPS诱导的RAW细胞264.7的抗炎活性
炎症被认为是各种慢性疾病的基本机制。巨噬细胞被炎症刺激激活,诱导炎症介质的释放,从而使炎症介质成为抗炎药物开发的一个有希望的靶点。以往的研究表明岩藻糖聚糖通过抑制促炎介质的释放而具有抗炎活性。本研究旨在通过观察马尾藻水岩藻聚糖粗提物对促炎细胞因子TNF-α、IL-1β、dan IL-6的影响来确定其抗炎活性。岩藻聚糖是一种多糖物质,其来源和提取方法的不同,使其具有不同的特性,影响了其生物活性。采用稀盐酸0.1 M提取西爪哇地区的马尾藻,用乙醇沉淀得到褐藻聚糖粗提物。采用ELISA法检测粗提物对lps诱导的RAW 264.7细胞TNF-α、IL-1β、IL-6水平的影响。结果表明,岩藻多糖粗提物在25和50 μg/ml剂量下可降低TNF-α水平,在25 μg/ml剂量下可降低IL-1β和IL-6水平。50 μg/ml剂量不能抑制IL-1β和IL-6的产生。结果表明,粗提物粗提物25 μg/ml时对raw264.7细胞具有抗炎活性。
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审稿时长
16 weeks
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