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人参属植物高温蒸制前后人参皂苷含量的变化和细胞毒活性研究
引用本文:顾承真,曾碧雪,张钰佳,王东,张颖君. 人参属植物高温蒸制前后人参皂苷含量的变化和细胞毒活性研究[J]. 中草药, 2021, 52(11): 3391-3397
作者姓名:顾承真  曾碧雪  张钰佳  王东  张颖君
作者单位:福建农林大学生命科学学院, 福建 福州 350001;中国科学院昆明植物研究所, 植物化学与西部植物资源可持续利用国家重点实验室, 云南 昆明 650201
基金项目:国家自然科学基金资助项目(31800332);福建农林大学杰出青年科研人才计划项目(XJQ201922);中国科学院昆明植物研究所植物化学与西部植物资源可持续利用国家重点实验室开放课题(P2018-KF13)
摘    要:目的 研究人参属植物人参Panax ginseng、三七P.notoginseng和西洋参P.quinquefolium高温蒸制前后主要人参皂苷的含量变化,并测定高温蒸制前后样品对4株肿瘤癌细胞的细胞毒活性.方法 采用HPLC建立了测定22种皂苷含量的分析方法,测定这些皂苷在人参属植物及其高温蒸制品中的含量.用MTT法...

关 键 词:人参  三七  西洋参  细胞毒活性  人参皂苷Rg1  人参皂苷Re  人参皂苷Rb1  人参皂苷Rc  人参皂苷Rb2  人参皂苷Rd  20(S/R)-人参皂苷Rg3  20(S/R)-人参皂苷Rs3  20(S/R)-人参皂苷Rk1  20(S/R)-人参皂苷Rg5
收稿时间:2020-09-06

Variation of ginsenosides in raw and processed ginsengs (Panax sp.) and their cytotoxicities
GU Cheng-zhen,ZENG Bi-xue,ZHANG Yu-ji,WANG Dong,ZHANG Ying-jun. Variation of ginsenosides in raw and processed ginsengs (Panax sp.) and their cytotoxicities[J]. Chinese Traditional and Herbal Drugs, 2021, 52(11): 3391-3397
Authors:GU Cheng-zhen  ZENG Bi-xue  ZHANG Yu-ji  WANG Dong  ZHANG Ying-jun
Affiliation:College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350001, China;State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
Abstract:Objective To study the changes in the content of the major ginsenosides of the raw roots and the steaming processed ones of three Panax plants, e.g. Renshen (Panax ginseng), Sanqi (Panax notoginseng) and Xiyangshen (Panax notoginseng) and evaluate the cytotoxicities of raw roots and the steaming processed ones of three Panax plants against four cancer cell lines. Methods An HPLC method was established to qualify the amounts of 22 saponins. The amounts of these saponins in the raw roots and the steaming processed ones were quantified. The cytotoxicities of the raw roots and the steaming processed ones against four cancer cell lines (human myeloid leukemia HL-60, hepatocellular carcinoma SMMC-7721, lung cancer A-549, and breast cancer SK-BR-3 cell lines) were evaluated by MTT methods. Results From them, 22 saponins, including ginsenosides Rg1, Re, Rb1, Rc, Rb2, Rd, Rk3, Rh4, Rk1, Rg5, Rb3, Rh3, Rk2, 20(S)-and 20(R)-ginsenoside Rh1, notoginsenosides Fc and R1, gypenoside IX, 20(S/R)-notoginsenoside Ft1, 20(S/R)-ginsenosides Rg3, Rs3, and Rh2 were identified. Among them, ginsenosides Rg1, Re, Rb1, Rc, Rb2and Rd, ginsenoside Rg1, Re, Rb1and Rd, and ginsenoside Rg1, Re, Rb1, Rd and notoginsenosides R1were found to be the major saponins in the raw roots of P. ginseng, P. quinquefolium, and P. notoginseng, respectively. However, after steaming process, they all changed to be ginsenosides Rk3, Rh4, Rk1, Rg5 and 20(S/R)-ginsenosides Rg3. In case of the steaming processed roots of P. notoginseng, two more ginsenosides, 20(S)-ginsenoside Rh1and 20(R)-ginsenoside Rh1 were also detected at the same time. Three saponins, notoginsenoside Fc, ginsenoside Rb3 and gypenoside IX were detected to be the major saponins in the leaves and stems of P. notoginseng, and after steaming process, most of them were changed to other eight saponins, 20(S/R)-notoginsenosides Ft1, Rg3, and Rs3, ginsenosides Rk1, Rg5, and 20(S/R)-ginsenoside Rh2, Rh3, Rk2. It was noted that the processed P. notoginseng was more cytotoxic than processed P. ginseng and processed P. quinquefolium. The activity of cytotoxicities of the processed P. notoginseng was better than that of raw P. notoginseng. It means that after steaming process, P. notoginseng become more cytotoxic against four cancer cell lines. Conclusion The main ingredients of three Panax plants disappeared and transformed to others. The cytotoxicities of processed P. notoginseng were stronger than others.
Keywords:Panax ginseng Meyer  Panax notoginseng (Burk.) F. H. Chen  Panax quinquefolium L.  cytotoxicity  ginsenosides Rg1  ginsenoside Re  ginsenoside Rb1  ginsenoside Rc  ginsenoside Rb2  ginsenoside Rd  20(S/R)-ginsenoside Rg3  20(S/R)-ginsenoside Rs3  20(S/R)-ginsenoside Rk1  20(S/R)-ginsenoside Rg5  gypenoside IX
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