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Ginsenoside Rk1 suppresses pro-inflammatory responses in lipopolysaccharide-stimulated RAW264.7 cells by inhibiting the Jak2/Stat3 pathway 被引量:21
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作者 YU Qian ZENG Ke-Wu +3 位作者 MA Xiao-Li JIANG Yong TU Peng-Fei WANG Xue-Mei 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2017年第10期751-757,共7页
The saponin ginsenoside Rk1 is a major compound isolated from ginseng.Ginsenoside Rk1 has been reported to have anti-inflammatory and anti-tumor properties and to be involved in the regulation of metabolism.However,th... The saponin ginsenoside Rk1 is a major compound isolated from ginseng.Ginsenoside Rk1 has been reported to have anti-inflammatory and anti-tumor properties and to be involved in the regulation of metabolism.However,the effect and mechanism of anti-inflammatory action of ginsenoside Rk1 has not been fully clarified.We investigated whether ginsenoside Rk1 could suppress the inflammatory response in lipopolysaccharide-stimulated RAW264.7 macrophages and to explore its mechanism of the action.RAW264.7 cells were treated with LPS(1 μg×mL^(–1))in the absence or the presence of Ginsenoside Rk1(10,20,and 40 μmol×L^(–1)).Then the inflammatory factors were tested with Griess reagents,ELISA,and RT-PCR.The proteins were analyzed by Western blotting.Ginsenoside Rk1 inhibited lipopolysaccharide-induced expression of nitric oxide(NO),interleukin(IL)-6,IL-1β,tumor necrosis factor(TNF)-α,and monocyte chemotactic protein(MCP)-1.Ginsenoside Rk1 inhibited the lipopolysaccharide-stimulated phosphorylation of NF-κB and janus kinase(Jak)2 and signal transducer and activator of transcription(Stat)3 at Ser727 and Tyr705.These data suggested that ginsenoside Rk1 could inhibit expression of inflammatory mediators and suppress inflammation further by blocking activation of NF-κB and the Jak2/Stat3 pathway in LPS-stimulated RAW264.7 cells. 展开更多
关键词 Inflammation RAW264.7 cells ginsenoside rkl JAK2/STAT3 NF-xB
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柠檬催化转化原人参二醇组皂苷制备人参皂苷Rg5的初步研究 被引量:12
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作者 孙成鹏 高维平 +1 位作者 赵宝中 成乐琴 《中成药》 CAS CSCD 北大核心 2013年第12期2694-2698,共5页
目的建立一种新的环境友好型的人参皂苷Rg5的制备方法。方法采用柠檬为催化剂,人参二醇组皂苷为原料,制备稀有人参皂苷Rg5,结合硅胶柱层析和半制备型高效液相色谱分离人参皂苷Rg5和Rk1,并通过HPLC和NMR进行定量分析和结构鉴定。结果原... 目的建立一种新的环境友好型的人参皂苷Rg5的制备方法。方法采用柠檬为催化剂,人参二醇组皂苷为原料,制备稀有人参皂苷Rg5,结合硅胶柱层析和半制备型高效液相色谱分离人参皂苷Rg5和Rk1,并通过HPLC和NMR进行定量分析和结构鉴定。结果原人参二醇组皂苷(20 mg/mL)与柠檬汁(80%)以1∶2.5混合,于100℃反应2 h,HPLC分析表明,人参皂苷Rb1、Rc、Rb2、Rb3和Rd的转化率均为100%,人参皂苷Rg5产率为30.77%。结论该方法操作简单,成本低,环境友好,对于研究人参皂苷Rg5的药理活性及开发相关保健品具有重要参考价值。 展开更多
关键词 柠檬 原人参二醇组皂苷 人参皂苷Rg5 人参皂苷Rk1 酸水解
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