In Vitro Immunomodulatory Activity of Fig Fruit Ethanol Extract (Ficus carica Linn) against Phagocytosis Macrophages and Lymphocyte Proliferation

Iis Nur Azizah, A. Winanta
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Abstract

Fig (Ficus carica L.)  is a natural product that potentially can improve the immune system because it has flavonoids that have the potential as immunostimulants. The research aims to determine the possibility of fig fruit ethanol extract as an immunomodulator. Immunomodulatory activity is determined by knowing the activity of macrophage phagocytosis and lymphocyte proliferation in vitro and the levels of flavonoids in the extract. The research began with extraction, and then the sample was tested with TLC and colorimetry methods. Furthermore, the sample in the immunomodulatory activity test in vitro was measured through the activity of macrophage phagocytosis and lymphocyte proliferation. In the phagocytosis activity test, macrophage cells were given samples in various concentrations and latex beads. The number of activated macrophages and the number of latex phagocyted by the macrophage is then calculated. For tests of lymphocyte proliferation activity, lymphocyte cells were sampled with different concentrations and induced hepatitis B vaccine. Then the cell absorbance was read with an Elisa reader at 550nm wavelength. The study results found that the samples contained flavonoid compounds, and the total flavonoid levels obtained were 0.74±0.01 mgEQ/g samples. The immunomodulatory activity showed that the sample increased phagocytosis activity of macrophages compared to cell control. The lymphocyte proliferation test produced stimulation index<2 values, showing no effect on the proliferation of lymphocytes. This study indicated that fig fruit ethanol extract could increase the phagocytosis activity of macrophage cells but did not affect the proliferation of lymphocyte cells in vitro.
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无花果乙醇提取物对吞噬细胞巨噬细胞和淋巴细胞增殖的体外免疫调节活性
无花果(Ficus carica L.)是一种天然产品,可以潜在地改善免疫系统,因为它含有黄酮类化合物,具有免疫刺激剂的潜力。本研究旨在确定无花果果乙醇提取物作为免疫调节剂的可能性。通过体外巨噬细胞吞噬活性和淋巴细胞增殖活性以及提取物中黄酮类化合物的含量来确定其免疫调节活性。研究从提取开始,然后用薄层色谱法和比色法对样品进行检测。此外,通过巨噬细胞吞噬活性和淋巴细胞增殖活性测定体外免疫调节活性试验样品。在吞噬活性试验中,给予巨噬细胞不同浓度的样品和乳胶珠。然后计算被激活的巨噬细胞数量和被巨噬细胞吞噬的乳胶数量。为了检测淋巴细胞的增殖活性,我们采集了不同浓度的淋巴细胞和诱导乙肝疫苗。然后用酶联免疫吸附仪在550nm波长下读取细胞吸光度。研究结果表明,样品中含有黄酮类化合物,得到的总黄酮含量为0.74±0.01 mgEQ/g样品。免疫调节活性表明,与对照组相比,该样品增加了巨噬细胞的吞噬活性。淋巴细胞增殖试验刺激指数<2,对淋巴细胞增殖无影响。本研究表明,无花果果乙醇提取物可以提高巨噬细胞的吞噬活性,但不影响淋巴细胞的体外增殖。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
10
审稿时长
15 weeks
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