首页> 外文期刊>Taiwan Veterinary Journal >EFFECTS OF TARAXACUMMONGOLICUM EXTRACT ON LIPOPOLYSACCHARIDE-INDUCEDNITRIC OXIDE AND CYTOKINES PRODUCTION BY BOVINE PERIPHERAL BLOOD MONONUCLEAR CELLS
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EFFECTS OF TARAXACUMMONGOLICUM EXTRACT ON LIPOPOLYSACCHARIDE-INDUCEDNITRIC OXIDE AND CYTOKINES PRODUCTION BY BOVINE PERIPHERAL BLOOD MONONUCLEAR CELLS

机译:蒲公英提取物对牛外周血单核细胞脂多糖诱导的一氧化氮和细胞因子产生的影响

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The objective of this study is to investigate Taraxacum mongolicum (TM) as a therapeutic alternative for preventing and treating bovine mastitis. The effect of the anti-inflammatory activity of Taraxacum mongolicum extract (TME) on lipopolysaccharide(LPS)-induced responses was studied in the bovine peripheral blood mononuclear cells (PBMCs). The dried plant TM was extracted with 10 volumes of distilled water to generate its water extract. PBMCs were pretreated with various concentrations of TME (0,1, 10, 100, 1000 /Ug/mL) and subsequently incubated with LPS (1 /mug/mL). Cell viability was analyzed by 3-(4,5-dime-thylthiazol-2-yl)-2,5-diphenylthiazolium bromide (MTT) assay. The level of nitric oxide (NO) was determined by using Griess reagent assay. The mRNA expression levels of pro-inflammatory cytokines including interleukin (IL)-l/3, IL-6, IL-8, tumor necrosis factor (TNF)-q and granulocyte chemotactic protein (GCP)-2 were determined by using quantitative reverse transcription-polymerase chainreaction (qRT-PCR). The results showed no significant cytotoxic effects on the PBMCs at various treated concentrations of TME. Treatment of TME (100 and 1000 /ug/mL) significantly inhibited NO production in LPS-stimulated PBMCs. TME (10 ug/mL) significantly inhibited LPS-stimulated IL-1/3, IL-6, IL-8, TNF-a and GCP-2 mRNA expression in PBMCs at a time-dependent manner. In this article, we reported for the first time
机译:这项研究的目的是研究蒲公英作为预防和治疗牛乳腺炎的替代治疗方法。在牛外周血单核细胞(PBMCs)中研究了蒙古蒲公英提取物(TME)的抗炎活性对脂多糖(LPS)诱导的反应的影响。用10倍体积的蒸馏水提取干燥的植物TM以产生其水提取物。 PBMC用各种浓度的TME(0,1、10、100、1000 / Ug / mL)预处理,然后与LPS(1 /μg/ mL)孵育。细胞存活力通过3-(4,5-二甲基-噻唑-2-基)-2,5-二苯基噻唑溴化物(MTT)分析进行分析。一氧化氮(NO)的水平通过使用格里斯试剂测定法确定。通过定量逆向测定白细胞介素(IL)-1 / 3,IL-6,IL-8,肿瘤坏死因子(TNF)-q和粒细胞趋化蛋白(GCP)-2等促炎细胞因子的mRNA表达水平。转录聚合酶链反应(qRT-PCR)。结果显示,在各种处理过的TME浓度下,对PBMC均无明显的细胞毒性作用。 TME(100和1000 / ug / mL)的处理显着抑制了LPS刺激的PBMC中NO的产生。 TME(10 ug / mL)以时间依赖性方式显着抑制PBMC中LPS刺激的IL-1 / 3,IL-6,IL-8,TNF-a和GCP-2 mRNA表达。在本文中,我们是第一次报道

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