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用另一种巴黎代替另一种巴黎?替代滇藏重楼的秀丽假福王草的体外细胞毒性和体内抗肿瘤活性。

Substituting one Paris for another? In vitro cytotoxic and in vivo antitumor activities of Paris forrestii, a substitute of Paris polyphylla var. yunnanensis.

机构信息

Key Laboratory of Economic Plants and Biotechnology and the Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, People's Republic of China; Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Yezin, Nay Pyi Taw 05282, Myanmar.

School of Pharmaceutical Sciences & Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming 650500, People's Republic of China.

出版信息

J Ethnopharmacol. 2018 May 23;218:45-50. doi: 10.1016/j.jep.2018.02.022. Epub 2018 Feb 15.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Chong-lou (Paris polyphylla var. yunnanensis or P. polyphylla var. chinensis) is traditionally used as an anticancer medicine in China. It is also the material basis of some Chinese patent anticancer medicines, such as Gan-Fu-Le capsules, Bo-Er-Ning capsules, Lou-Lian capsules, Ruan-Jian oral liquid, and Qi-Zhen capsules. P. forrestii, a substitute for Chong-lou, is planted at a large scale in the Yunnan Province of China.

AIM OF THE STUDY

To clarify the active chemical constituents of P. forrestii and evaluate the in vitro and in vivo anticancer activities of the total saponins from P. forrestii.

MATERIALS AND METHODS

The total saponins of P. forrestii were extracted and separated to yield pure compounds by chromatographic techniques, and the structures of the isolates were elucidated by spectroscopic methods. The cytotoxicity of the crude extracts, total saponins, and chemical constituents were evaluated using an MTS assay. In vivo antitumor activities of the total saponins from P. forrestii were measured using H22 tumor-bearing mice by intraperitoneal (ip) administration.

RESULTS

Eight compounds, including polyphyllin D (1), formosanin C (2), dioscin (3), diosgenin-3-O-α-l-rhamnopyranosyl-(1→2)-β-d-glucopyranoside (4), paris saponin H (5), pennogenin-3-O-α-l-rhamnopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→4)]-β-d-glucopyranoside (6), pariposide A (7), and crustecdysone (8), were isolated from the total saponins of P. forrestii. The total saponins and compounds 1-6 showed significant inhibitory activity against the growth of the HL-60, SMMC-7721, A-549, MCF-7, and SW480 cell lines. The total saponins from P. forrestii had a tumor-inhibitory effect in H22 tumor-bearing mice upon ip (2.25 mg/kg dose) administration, with an inhibition rate of 42.6% compared with cisplatin (ip, 2 mg/kg dose, 53.9% inhibition rate).

CONCLUSION

The results support that P. forrestii could be a substitute for P. polyphylla var. yunnanensis as an anticancer medicine.

摘要

民族药理学相关性

重楼(云南重楼或中国重楼的变种)传统上在中国被用作抗癌药物。它也是一些中国专利抗癌药物的物质基础,如肝复乐胶囊、博尔宁胶囊、六神胶囊、软肝口服液和奇珍胶囊。重楼的替代品云南重楼已在中国云南省大规模种植。

研究目的

阐明云南重楼的活性化学成分,并评价云南重楼总皂苷的体外和体内抗癌活性。

材料与方法

采用色谱技术从云南重楼中提取和分离总皂苷,采用光谱方法解析分离物的结构。采用 MTS 法评价粗提取物、总皂苷和化学成分的细胞毒性。采用腹腔(ip)给药法,以 H22 荷瘤小鼠为模型,测定云南重楼总皂苷的体内抗肿瘤活性。

结果

从云南重楼总皂苷中分离得到 8 种化合物,包括重楼皂苷 D(1)、薯蓣皂苷 C(2)、薯蓣皂苷元-3-O-α-L-鼠李吡喃糖苷基-(1→2)-β-D-吡喃葡萄糖苷(4)、重楼皂苷 H(5)、偏诺皂苷元-3-O-α-L-鼠李吡喃糖苷基-(1→2)-[α-L-鼠李吡喃糖苷基-(1→4)]-β-D-吡喃葡萄糖苷(6)、偏诺苷 A(7)和蜕皮甾酮(8)。总皂苷及化合物 1-6 对 HL-60、SMMC-7721、A-549、MCF-7 和 SW480 细胞系的生长均有显著抑制作用。云南重楼总皂苷 ip(2.25mg/kg 剂量)给药对 H22 荷瘤小鼠有抑瘤作用,抑制率为 42.6%,与顺铂(ip,2mg/kg 剂量,抑制率 53.9%)相比。

结论

结果支持云南重楼可替代云南重楼 var. yunnanensis 作为抗癌药物。

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