癌变·畸变·突变

• 检测研究 • 上一篇    下一篇

藏茵陈总萜酮的致突变及抗突变作用

王  冲,侯  娟,韩  晶,芮  菁*   

  1. 天津市药品检验所药理室,天津  300070
  • 收稿日期:2013-07-08 修回日期:2014-02-26 出版日期:2014-05-30 发布日期:2014-05-30
  • 通讯作者: 芮 菁,E-mail:rui599@sina.com
  • 作者简介:王冲(1983- ),男,山东人,硕士,药师,研究方向:中药

The safety and anti-mutagenicity of total terpene ketones from Swertia mussotii

WANG Chong,HOU Juan,HAN Jing,RUI Jing *   

  1. Pharmaceutical Department of Tianjin Institute for Drug Control, Tianjin 300070, China
  • Received:2013-07-08 Revised:2014-02-26 Online:2014-05-30 Published:2014-05-30

摘要:

目的:研究藏茵陈总萜酮的致突变及抗突变作用。方法:致突变实验采用Ames实验及小鼠体内微核实验。Ames实验采用常规掺入法;微核实验采用连续灌胃给药10 d的骨髓嗜多染红细胞微核计数法。抗突变实验采用体内、体外两种方法,体外法选用TA100及TA102菌株与环磷酰胺(每皿200 μg)和丝裂霉素C(每皿2 μg)共孵育30 min后,分别给予藏茵陈总萜酮每皿156、312、625、1 250及2 500 μg,检测其对阳性剂诱发的已突变菌落的保护作用;体内实验采用藏茵陈总萜酮25、50及100 mg/kg小鼠连续灌胃给药10 d后,给予40 mg/kg环磷酰胺或2 mg/kg丝裂霉素C,计算微核率,检测其对未发生突变的骨髓细胞的保护作用。结果:致突变实验中,藏茵陈总萜酮在每皿< 2 500 μg剂量下,未诱发Ames实验各菌株回变菌落数增加;在每皿< 40 mg/kg剂量下,未诱发骨髓嗜多染红细胞微核率增高。抗突变实验中,藏茵陈总萜酮在每皿625~ 2 500 μg范围内,可使阳性致突变剂环磷酰胺和丝裂霉素C所诱发的高回变菌落数出现明显降低;藏茵陈总萜酮在50~ 100 mg/kg剂量范围,可使阳性剂环磷酰胺或丝裂霉素C所诱发的高微核率出现明显降低。结论:本实验条件下,藏茵陈总萜酮未表现出诱导基因突变和染色体畸变作用,且有显著的抗突变作用。

关键词: 藏茵陈总萜酮, Ames实验, 微核实验, 致突变, 抗突变

Abstract:

OBJECTIVE: To study the mutagenic and anti-mutagenic activities of total terpene ketones from Swertia mussotii (TTKS) at different doses. METHODS:Mutagenic experiments:conventional Ames test and micronucleus test were selected. Ames experiment was used with the incorporation method. Micronucleus test was conducted in mice which were treated orally once a day for 10 days consecutively. Anti-mutagenic experiments:methods in vitro,pre-incubated the TA100 and TA102 strains with CP (200 μg/plate) or MMC ( 2 μg/plate) for 30 minutes,then mixed the above materials with TTKS ( 156,312,625,1 250 and 2 500 μg/plate ),so as to detect the protective effects of TTKS on mutational colonies induced by positive agent. Mice were exposed to CP (40 mg/kg) or MMC (2 mg/kg) after continuous irrigation of TTKS (25,50 and 100 mg/kg ) for 10 days,the micronucleus rate was calculated in order to detect the protective effects of TTKS on non-mutation bone marrow cells. RESULTS:In mutagenic test,TTKS at a dose lower than 2 000 μg/plate induced no obvious increase in mutagenicity of the four strains. TTKS at a dose lower than 40 mg/kg did not increase the micronucleus frequencies of polychromatic erythrocytes. In anti-mutagenic test,comparing with the positive groups of CP and MMC,TTKS at 625-2 500 μg/plate could decrease the colony numbers in T100 and T102 strains. TTKS at 50-100 mg/kg could significantly reduce the rate of micronucleus of polychromatic erythrocytes in mice bone marrow induced by CP and MMC as compared with the positive control. CONCLUSION:Under these experimental conditions,TTKS showed no effect of mutagenesis and could confer significant anti-mutagenic protection.

Key words: total terpene ketones from Swertia mussotii, Ames test, micronucleus test, mutagenicity, anti-mutagenicity