天然产物研究与开发 ›› 2026, Vol. 38 ›› Issue (9): 1972-1979.doi: 10.16333/j.1001-6880.2026.9.011 cstr: 32307.14.1001-6880.2026.9.011

• 开发研究 • 上一篇    下一篇

红芪、黄芪蜜炙前后配伍醋莪术含药血清对肺癌细胞增殖、迁移和侵袭的影响

马定财 1,2,刘  婷 1,2,杜欣霞 1,2, 巩文林 1,2,张育贵 2,辛二旦 1,2,边甜甜 1,李越峰 2∗   

  1. 1甘肃中医药大学药学院;2 甘肃中医药大学科研实验中心,兰州730000

  • 出版日期:2026-09-24 发布日期:2026-09-22
  • 基金资助:

    国家自然科学基金(82574743、82560778);2024 年甘肃省人才重点项目(2024RCXM77);2024 年甘肃省联合科研基金(24JRRA882)

Effects of containing serum from Hedysari Radix and Astragali Radix before and after honey-processing paired with vinegar-processed Curcumae Rhizoma on the proliferation,migration and invasion of lung cancer cells

MA Ding-cai1,2,LIU Ting1,2,DU Xin-xia1,2, GONG Wen-lin1,2,ZHANG Yu-gui2,XIN Er-dan1,2,BIAN Tian-tian1,LI Yue-feng2∗   

  1. 1College of Pharmacy,Gansu University of Chinese Medicine; 2 Scientific Research and Experimental Center,Gansu University of Chinese Medicine,Lanzhou 730000,China

  • Online:2026-09-24 Published:2026-09-22

摘要:

研究红芪(Hedysari Radix,HR)、黄芪(Astragali Radix,AR)蜜炙(honey processed,HP)前后配伍醋莪术(vinegar-processed Curcumae Rhizoma,VPCR)对A549 和NCI-H1299 细胞增殖、迁移和侵袭的影响。将49 只SD 雄性大鼠随机分为AR-VPCR、HPAR-VPCR、HR-VPCR、HPHR-VPCR、顺铂(cis-diaminodichloroplatinum,CDDP) + HPHR-VPCR 含药血清组、CDDP 组和空白组,连续灌胃7 d,采集血清;采用CCK-8 法筛选CDDP 抗A549 细胞的最佳浓度。集落实验检测细胞克隆能力,流式细胞术检测细胞周期,划痕实验检测细胞迁移能力,Transwell 小室实验检测细胞侵袭能力。结果发现,CDDP 干预A549 细胞和NCI-H1299 细胞的最佳浓度分别是20. 99、15. 25 mg/ L。AR-VPCR、HPARVPCR、HR-VPCR、HPHR-VPCR、CDDP、CDDP + HPHR-VPCR 均显著抑制A549 细胞和NCI-H1299 细胞克隆、迁移和侵袭(P < 0. 01)。在抑制细胞克隆方面,HR-VPCR 组优于AR-VPCR 组,HPHR-VPCR 优于HPAR-VPCR 组,HPHRVPCR 组抑制2 株细胞克隆的作用更明显。在抑制细胞迁移方面,HPHR-VPCR 联合CDDP 可增强抑制作用,HPARVPCR 强于AR-VPCR 组。AR-VPCR、HPAR-VPCR、HR-VPCR、HPHR-VPCR 将A549 细胞和NCI-H1299 细胞DNA 复制阻滞在G1 期,CDDP、CDDP + HPHR-VPCR 将A549 细胞DNA 复制阻滞在S 期。综上,AR-VPCR、HPAR-VPCR、 HR-VPCR、HPHR-VPCR、CDDP、CDDP + HPHR-VPCR 均可显著影响细胞周期,抑制A549 细胞和NCI-H1299 细胞克隆、迁移和侵袭。

关键词:

"> 炙红芪-醋莪术, 肺癌, 增殖, 迁移和侵袭

Abstract:

This study aims to investigate the effects of Hedysari Radix (HR),Astragali Radix (AR),and their combinations with vinegar-processed Curcumae Rhizoma (VPCR) before and after honey processing (HP) on the proliferation,migration, and invasion of A549 and NCI-H1299 cells. Forty-nine male SD rats were randomly divided into seven groups:AR-VPCR, HPAR-VPCR,HR-VPCR,HPHR-VPCR,cis-diaminodichloroplatinum(CDDP) + HPHR-VPCR containing serum,CDDP,and control group. Serum was collected after seven consecutive days of intragastric administration. The optimal concentration of CDDP against A549 cells was screened by the CCK-8 assay. Colony formation assay was used to detect cell clonogenicity,flow cytometry to analyze the cell cycle,wound-healing assay to evaluate cell migration,and Transwell chamber assay to measure cell invasion. The results showed that the optimal concentrations of CDDP for A549 and NCI-H1299 cells were 20. 99 and 15. 25 mg/ L,respectively. AR-VPCR,HPAR-VPCR,HR-VPCR,HPHR-VPCR,CDDP,and CDDP + HPHR-VPCR all significantly inhibited colony formation,migration,and invasion of A549 and NCI-H1299 cells (P < 0. 01). In terms of colony inhibition,the HR-VPCR group was superior to the AR-VPCR group,and the HPHR-VPCR group was superior to the HPARVPCR group,with HPHR-VPCR showing stronger inhibitory effects on both cell lines. For migration inhibition,the combination of HPHR-VPCR and CDDP exerted a synergistic inhibitory effect,and HPAR-VPCR was more effective than AR-VPCR. AR-VPCR,HPAR-VPCR,HR-VPCR,and HPHR-VPCR arrested DNA replication of A549 and NCI-H1299 cells in the G1 phase,while CDDP and CDDP + HPHR-VPCR blocked DNA replication of A549 cells in the S phase. In conclusion,ARVPCR,HPAR-VPCR,HR-VPCR,HPHR-VPCR,CDDP,and CDDP + HPHR-VPCR can significantly affect the cell cycle and inhibit colony formation,migration,and invasion of A549 and NCI-H1299 cells.

Key words:

"> honey-processed Hedysari Radix-vinegar-processed Curcumae Rhizoma, lung cancer, proliferation, migration and invasion

中图分类号: 

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