首页> 外文期刊>Pharmaciana >EFEK FRAKSI ETIL ASETAT EKSTRAK ETANOL AKAR PASAK BUMI (Eurycoma longifolia, Jack) TERHADAP AKTIVITAS FAGOSITOSIS MAKROFAG SECARA IN VITRO
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EFEK FRAKSI ETIL ASETAT EKSTRAK ETANOL AKAR PASAK BUMI (Eurycoma longifolia, Jack) TERHADAP AKTIVITAS FAGOSITOSIS MAKROFAG SECARA IN VITRO

机译:木瓜BUMI(长叶Eurycoma,Jack)的乙酸乙酯提取物对体外磷酸化酶活性的影响

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Eurycoma longifolia has been used as a remedy for detoxification, aphrodisiaca, anticancer and immunistimulant. The quassinoids of pasak bumi root extract, have antioxidant activity and immunomodulatory activity by increasing IL-12. This study aims to determine the effect of the ethyl acetate fraction of ethanolic extract of pasak bumi root on macrophages phagocytic activity in vitro. Macrophages were isolated from peritoneal fluid of male Balb/Cmice, and thenwere cultured for 24 hours in 24 well plate. The ethyl actetate fraction ethanolic extract of pasak bumi root with concentration of 10, 50, and 100 μg/ml, lipopolysaccharides and dimethyl sulfoxide were added, and incubated for 1.5 hours. The phagocytosis tests was carried out by adding latex with density 5x104 /well and incubated for 1.5 hours at incubator (5% CO2,37o C). Macrophage were then stained by Giemsa. The results showed that the percentage of active phagocytic cells treated with ethyl actetate fraction of ethanolic extract of pasak bumi root of 10, 50 and 100 μg/ml, lipopolysaccharides, and dimethyl sulfoxide were 95.4%, 90%, 85.4%, 83.4%, and 79% respectively. Phagocytic capacity at treatment levels of 10, 50, and 100 μg/ml, lipopolysaccharides,and dimethyl sulfoxide were 469; 439.8; 360.8; 204.6; and 147.6 respectively. The result showed thatreatment of ethyl acetate fraction of ethanolic extract of pasak bumi root can increase the phagocytic activity of macrophages in vitro.
机译:长叶杜仲被用作排毒,壮阳药,抗癌药和免疫刺激药。木瓜根提取物的类quasinoids通过增加IL-12具有抗氧化活性和免疫调节活性。本研究旨在确定木瓜根乙醇提取物的乙酸乙酯级分对体外巨噬细胞吞噬活性的影响。从雄性Balb / Cmice的腹膜液中分离巨噬细胞,然后在24孔板中培养24小时。添加浓度分别为10、50和100μg/ ml的木瓜根的乙酸乙酯馏分乙醇提取物,脂多糖和二甲基亚砜,并孵育1.5小时。通过加入密度为5x104 /孔的乳胶进行吞噬试验,并在培养箱(5%CO2,37°C)下培养1.5小时。然后巨噬细胞被吉姆萨染色。结果显示,以10、50和100μg/ ml的木瓜根乙醇提取物的乙酸乙酯馏分,脂多糖和二甲基亚砜处理的活性吞噬细胞百分比分别为95.4%,90%,85.4%,83.4%,和79%。处理水平分别为10、50和100μg/ ml,脂多糖和二甲亚砜的吞噬能力为469; 439.8; 360.8; 204.6;和147.6。结果表明,处理木瓜根乙醇提取物的乙酸乙酯级分可以提高巨噬细胞的吞噬活性。

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