首页|期刊导航|中国免疫学杂志|红芪拆分组分对巨噬细胞吞噬功能的影响

红芪拆分组分对巨噬细胞吞噬功能的影响OA

Effect of fractionation from Hedysari Radix on phagocytic function of macrophage

中文摘要英文摘要

目的:研究红芪拆分组分对巨噬细胞吞噬功能的影响.方法:通过化学方法拆分红芪组分并进行含量测定;高效液相排阻色谱-光散射-示差串联检测法(HPSEC-MALLS-RI)测定多糖分子量;并研究拆分组分体外抗氧化能力;CCK-8法研究拆分组分对巨噬细胞活力的影响;流式细胞术检测拆分组分对巨噬细胞吞噬功能的影响;Griess法和ELISA检测拆分组分对巨噬细胞一氧化氮(NO)、TNF-α、IFN-γ和IL-1β分泌水平的影响.结果:红芪拆分为脱蛋白多糖(HPS)、分段多糖HG-2、HG-3、HG-4、乙酸乙酯萃取物(EtOAc)、正丁醇萃取物(nBuOH)和氨基酸(AA)7个组分;EtOAc中黄酮含量为3.80%,nBuOH中皂苷含量为26.03%,氨基酸含量为0.40%,分段多糖HG-2、HG-3和HG-4的含量分别为81.35%、88.87%和82.53%.分段多糖HG-2、HG-3和HG-4的分子量分别为76.49、83.73和118.55 kD.体外抗氧化结果表明,当样品浓度在1.0~2.5 μg/mL时,EtOAc组和nBuOH组对DPPH自由基的清除率较高(P<0.01);HPS和分段多糖对超氧阴离子自由基的清除率和总还原力的作用较为突出.7个拆分组分在 12.5~25.0 μg/mL 浓度范围内对巨噬细胞均无显著的细胞毒性;除AA外,其余6个组分均可显著增强巨噬细胞对模式抗原的吞噬作用(P<0.01),其中nBuOH、HPS和EtOAc促进巨噬细胞吞噬的作用较强,且6个组分均能刺激巨噬细胞分泌NO、TNF-α、IFN-γ、IL-1β(P<0.01).结论:红芪7个拆分组分中,除AA外,HPS、分段多糖HG-2、HG-3、HG-4、EtOAc和nBuOH 6组分均可激活巨噬细胞,增强巨噬细胞的吞噬功能,从而增强其免疫活性,且nBuOH、HPS和EtOAc活性较强.

Objective:To investigate the effects of fractionation from Hedysari Radix on the immunological function by regulat-ing phagocytic of macrophages.Methods:The fraction of Hedysari Radix was chemically resolved and the content was determined;high performance liquid phase exclusion chromatography-light scattering-differential tandem detection(HPSEC-MALLS-RI)was used to determine the molecular weight of polysaccharides;and studying the antioxidant capacity of split groups in vitro;the effects of frac-tionation from Hedysari Radix on the viability of macrophage were studied by the CCK-8 method.The effects of fractionation on the phagocytosis of macrophage were investigated by flow cytometry.The effects of fractionation on the secretion of nitric oxide(NO),TNF-α,IFN-γ,and IL-1β were detected by Griess assay and ELISA.Results:Hedysari Radix was divided into 7 components:Depro-teopolysaccharides(HPS),segmented polysaccharide HG-2,HG-3,HG-4,ethyl acetate extract(EtOAc),n-butanol extract(nBuOH)and amino acid(AA),the content of flavonoids in the extraction site of EtOAc was 3.80%,the content of saponins in the extraction site of nBuOH was 26.03%,the content of amino acids was 0.40%,and the contents of segmented polysaccharides HG-2,HG-3 and G-4 were 81.35%,88.87%and 82.53%,respectively.The molecular weights of segmented polysaccharides HG-2,HG-3 and HG-4 were 76.49,83.73 and 118.55 kD,respectively.The results of in vitro antioxidant showed that when the sample concentration was 1.0~2.5 μg/mL,the scavenging rate of DPPH free radicals was higher in the EtOAc extract group and nBnOH group(P<0.01).The effects of deproteopolysaccharides and segmented polysaccharides on the scavenging rate and total reducing power of superoxide anion radi-cals were prominent.The 7 fractions had no significant cytotoxicity to macrophages in the concentration range of 12.5~25 μg/mL.Ex-cept for AA,the other six components could significantly enhance the phagocytosis of macrophages to model antigens(P<0.01),among which nBuOH,HPS and EtOAc had astronger effect on macrophage phagocytosis,and the other six components could stimu-late macrophages to secrete NO,TNF-α,IFN-γ and IL-1β(P<0.01).Conclusion:In addition to AA,HPS,segmented polysaccha-ride HG-2,HG-3,HG-4,EtOAc and nBuOH 6 components can activate macrophages,enhance the phagocytic function of macro-phages,thereby enhancing their immune activity,and the activities of nBuOH,HPS and EtOAc are stronger.

王露;杨子牧;杨苗苗;庞哲;朱昕宇;邵晶;崔治家

甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000||西北中藏药协同创新中心,兰州 730000||甘肃省中药制药工艺工程研究中心,兰州 730000甘肃中医药大学药学院,兰州 730000||国家中医药管理局三级实验室(中药化学重点实验室),兰州 730000||西北中藏药协同创新中心,兰州 730000||甘肃省中药制药工艺工程研究中心,兰州 730000甘肃中医药大学药学院,兰州 730000||西北中藏药协同创新中心,兰州 730000

医药卫生

红芪拆分组分巨噬细胞吞噬

Hedysari RadixFractionationMacrophagePhagocytosis

《中国免疫学杂志》 2026 (8)

1793-1802,10

国家药监局中药材及饮片质量控制重点实验室项目(2024GSMPA-KL14)甘肃省科技计划项目(25JRRA1175)兰州市第三批科技计划项目科技支撑专项(2024-3-35)甘肃省科技计划东西协作专项(鲁甘科技协作项目,22CX8NA068).

10.3969/j.issn.1000-484X.2026.08.001

评论