天然产物研究与开发 ›› 2026, Vol. 38 ›› Issue (8): 1661-1669.doi: 10.16333/j.1001-6880.2026.8.004 cstr: 32307.14.1001-6880.2026.8.004

• 研究论文 • 上一篇    下一篇

红芪蜜炙前后配伍醋莪术对肺癌细胞凋亡、自噬的影响

马定财1,2,王  哲1,2,王毛毛1,2,张育贵1,2,辛二旦1,2,边甜甜1,2,刘  婷1,2,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:2026-08-27 发布日期:2026-08-26
  • 基金资助:
    国家自然科学基金(82160750);2024年甘肃省人才重点项目(2024RCXM77);2024年高校产业支撑计划(2024CYZC-41);2024年甘肃省联合科研基金(24JRRA882)

Effects of Hedysari Radix before and after honey-processing paired with vinegar-processed Curcumae Rhizoma on apoptosis and autophagy of lung cancer cells

MA Ding-cai1,2,WANG Zhe1,2,WANG Mao-mao1,2,ZHANG Yu-gui1,2,XIN Er-dan1,2,BIAN Tian-tian1,2,LIU Ting1,2,LI Yue-feng 2*   

  1. 1College of Pharmacy,Gansu University of Chinese Medicine;2 Scientific Researsh and Experimental Center,Gansu University of Chinese Medicine,Lanzhou 730000,China
  • Online:2026-08-27 Published:2026-08-26

摘要:

研究炙红芪-醋莪术(honey processed Hedysari Radix-vinegar-processed Curcumae Rhizoma,HPHR-VPCR)和红芪-醋莪术(Hedysari Radix-vinegar-processed Curcumae Rhizoma,HR-VPCR)对A549细胞和NCI-H1299细胞凋亡和自噬的影响,并探讨HPHR-VPCR诱导凋亡和自噬的机制。将21只SPF级SD大鼠随机分为3组:空白(control,Con)组、HR-VPCR组、HPHR-VPCR组,各药对给药剂量均为4.63 g/kg,连续给药7 d后取含药血清;采用Hoechst33258染色检测细胞凋亡形态,流式细胞术检测细胞凋亡率;单丹磺酰尸胺(monodansylcadaverine,MDC)法检测细胞自噬情况;透射电镜检测自噬小体和自噬溶酶体;Western blot分别检测泛素结合蛋白P62(ubiquitin-binding protein P62,P62)、苄氯素1(beclin 1,BECN1)、B淋巴细胞瘤-2(B-cell lymphoma-2,BCL-2)、BCL-2相关X蛋白(BCL-2 associated X protein,BAX)蛋白的表达情况。Hoechst33258和流式细胞术检测结果显示,HR-VPCR和HPHR-VPCR组细胞染色质积累、细胞核浓缩和碎片化严重、凋亡荧光增强、凋亡比例增加;MDC法检测结果显示,HR-VPCR和HPHR-VPCR组绿色荧光增强,自噬体增加;Western blot结果显示,与Con组比较,HPHR-VPCR组P62、BCL-2蛋白表达显著降低,而BECN1、BAX蛋白表达显著升高(P<0.01,P<0.05)。综上,HR-VPCR和HPHR-VPCR均可诱导细胞凋亡和自噬,HPHR-VPCR在诱导细胞凋亡和自噬方面优于HR-VPCR。HPHR-VPCR诱导肺癌细胞凋亡和自噬的作用与P62、BCL-2降低,BECN1、BAX表达升高有关。

关键词:

红芪-醋莪术, 炙红芪-醋莪术, 肺癌细胞, 凋亡, 自噬

Abstract:

This study aims to compare the effects of honey processed Hedysari Radix-vinegar-processed Curcumae Rhizoma (HPHR-VPCR) and Hedysari Radix-vinegar-processed Curcumae Rhizoma (HR-VPCR) on apoptosis and autophagy in A549 cells and NCI-H1299 cells, and explore the mechanism of HPHR-VPCR inducing apoptosis and autophagy. Twenty-one SPF grade SD rats were randomly divided into three groups: control (Con) group, HR-VPCR group, and HPHR-VPCR group. The dosage of each drug pair was 4.63 g/kg, and the drug containing serum was taken after continuous administration for seven days; Hoechst33258 staining was used to detect cell apoptosis morphology, and flow cytometry was used to detect cell apoptosis rate; The monodansylcadaverine (MDC) method was used to detect cellular autophagy; Transmission electron microscopy was used to detect autophagosomes and autolysosomes; Western blot was used to detect the expression of ubiquitin-binding protein P62 (P62), beclin1(BECN1), B-cell lymphoma-2 (BCL-2), and BCL-2 associated X protein (BAX) proteins. The results of Hoechst33258 and flow cytometry analysis showed that in the groups treated with HR-VPCR and HPHR-VPCR, chromatin accumulation, nuclear concentration and fragmentation were severe, apoptosis fluorescence was enhanced, and the proportion of apoptosis increased; The MDC method detection results showed that the green fluorescence of the HR-VPCR group and HPHR-VPCR group was enhanced, and autophagosomes were increased; The Western blot results showed that compared with the blank group, the expression of P62 and BCL-2 proteins was significantly reduced in HPHR-VPCR group, while the expression of BECN1 and BAX proteins was significantly increased (P<0.01, P<0.05). In summary, both HR-VPCR and HPHR-VPCR can induce cell apoptosis and autophagy. HPHR-VPCR is superior to HR-VPCR in inducing cell apoptosis and autophagy. The induction of apoptosis and autophagy in lung cancer cells by HPHR-VPCR is related to the decrease of P62 and BCL-2, as well as the increase of BECN1 and BAX expression.

Key words:

Hedysari Radix-vinegar-processed Curcumae Rhizoma, honey-processed Hedysari Radix-vinegar-processed Curcumae Rhizoma; lung cancer cells, apoptosis, autophagy

中图分类号:  R283.1 R285.5