中国天然药物
中國天然藥物
중국천연약물
CHINESE JOURNAL OF NATRUAL MEDICINES
2008年
5期
367-371
,共5页
岳庆喜%关树宏%谢付波%宋肖依%马超%冯利兴%刘璇%果德安
嶽慶喜%關樹宏%謝付波%宋肖依%馬超%馮利興%劉璇%果德安
악경희%관수굉%사부파%송초의%마초%풍리흥%류선%과덕안
灵芝%灵芝三萜%相互作用%紫杉醇%顺铂
靈芝%靈芝三萜%相互作用%紫杉醇%順鉑
령지%령지삼첩%상호작용%자삼순%순박
Ganoderma lucidum%Ganoderma triterpenes%Interaction%Docetaxei%Cisplatin
目的:灵芝三萜类化合物是常被用于辅助性肿瘤治疗的灵芝中具有细胞毒性作用的主要成分.本研究考察灵芝总三萜和化疗药物之间的相互作用.方法:应用了两种肿瘤细胞株即人宫颈瘤HeLa细胞株和人非小细胞肺癌A549细胞株.检测了将灵芝总三萜与紫杉醇或顺铂合用时对细胞的毒性作用,并用Chou and Talalay合用指数法判断合用的相互作用类型.结果:灵芝总三萜和紫杉醇的合用在HeLa细胞中表现为协同作用而在A549细胞中表现为加合作用.灵芝总三萜与顺铂的合用效果则依赖于该两种药物的作用强度,即当其中一种药物的作用强于另外一种时表现为拮抗作用,而当两种药物的作用相似时表现为协同作用.结论:灵芝总三萜可以促进某些化疗药物的作用.
目的:靈芝三萜類化閤物是常被用于輔助性腫瘤治療的靈芝中具有細胞毒性作用的主要成分.本研究攷察靈芝總三萜和化療藥物之間的相互作用.方法:應用瞭兩種腫瘤細胞株即人宮頸瘤HeLa細胞株和人非小細胞肺癌A549細胞株.檢測瞭將靈芝總三萜與紫杉醇或順鉑閤用時對細胞的毒性作用,併用Chou and Talalay閤用指數法判斷閤用的相互作用類型.結果:靈芝總三萜和紫杉醇的閤用在HeLa細胞中錶現為協同作用而在A549細胞中錶現為加閤作用.靈芝總三萜與順鉑的閤用效果則依賴于該兩種藥物的作用彊度,即噹其中一種藥物的作用彊于另外一種時錶現為拮抗作用,而噹兩種藥物的作用相似時錶現為協同作用.結論:靈芝總三萜可以促進某些化療藥物的作用.
목적:령지삼첩류화합물시상피용우보조성종류치료적령지중구유세포독성작용적주요성분.본연구고찰령지총삼첩화화료약물지간적상호작용.방법:응용료량충종류세포주즉인궁경류HeLa세포주화인비소세포폐암A549세포주.검측료장령지총삼첩여자삼순혹순박합용시대세포적독성작용,병용Chou and Talalay합용지수법판단합용적상호작용류형.결과:령지총삼첩화자삼순적합용재HeLa세포중표현위협동작용이재A549세포중표현위가합작용.령지총삼첩여순박적합용효과칙의뢰우해량충약물적작용강도,즉당기중일충약물적작용강우령외일충시표현위길항작용,이당량충약물적작용상사시표현위협동작용.결론:령지총삼첩가이촉진모사화료약물적작용.
AIM: Ganoderma triterpenes (GTS) are the main components with cytotoxicity in Ganoderma lucidum,a popularly used traditional Chinese Medicine (TCM) for complementary cancer therapy.The present study was designed to investigate the possible interaction between Ganoderma triterpenes and chemotherapeutics.METHODS: Cultures of human cervical carcinoma HeLa cells and human non-small lung carcinoma A549 cells were used.The cytotoxic effects-of GTS in combination with docetaxel (TXT) or eisplatin (CDDP) on cells were examined and the combination effects were analyzed by the Cbou and Talalay combination index method.RESULTS: The combinations targeting GTS with TXT resulted in a synergistic interaction in HeLa cells and an additive interaction in A549 cells.While,in both HeLa and A549 cells,the interactions between GTS and CDDP depended on the relative potency of their cytotoxicity.The interaction was antagonism when the cytotoxicity of GTS or CDDP was stronger than that of the other and was synergism when the cytotoxicity of the two medicines was similar.CONCLUSION: GTS could enhance the cytotoxieity of some kinds of chemotherapeutics but not all ehemotherapeutics against human carcinoma cells.