7种化合物细胞毒性与小鼠急性毒性的相关性研究  被引量:4

Research on correlations between cytotoxicity and acute toxicity of seven compounds

在线阅读下载全文

作  者:刘密凤[1] 彭双清[1] 盛治国[1] 解跃华[1] 董延生[1] 阳海鹰[1] 韩刚[1] 闫长会[1] 

机构地区:[1]中国人民解放军疾病预防控制所,毒理学评价研究中心,北京100850

出  处:《中国临床药理学与治疗学》2008年第1期42-45,共4页Chinese Journal of Clinical Pharmacology and Therapeutics

基  金:国家科技支撑计划"食品安全关键技术"重大项目(2006BAK02A02)

摘  要:目的:为减少实验动物的使用,利用化学物质的体外细胞毒性数据对体内急性毒性进行预测。方法:MTT比色法检测7种新化学实体对CHL细胞的毒性作用,利用RC(Registry of Cytotox-icity)预测模型对急性毒性LD50值进行预测,并使用小鼠急性毒性上下法进行验证。结果:各化合物(1~7)细胞毒性IC50值分别为0.43、0.49、0.18、0.67、3.03、1.68、1.79mg/mL;根据RC预测模型,急性毒性LD50的预测值分别为2376.4、2478.3、1574.8、2087.6、4897.3、3331.8、3300.7mg/kg。经上下法检测,4号化合物的LD50值为1634.0mg/kg,其余6种化合物的LD50值均大于2000.0mg/kg。分别以预测值和实测值为依据对化合物毒性进行分级,二者相比,仅3号和4号化合物毒性分级略有差异,其它5种化合物的毒性分级基本一致。结论:体外细胞毒性数据可用来预测体内急性毒性,减少实验动物使用。AIM: The study was undertaken to estimate acute toxicity in vivo using cytotoxicity data in vitro, in order to reduce animal usage in acute toxicity testing. METHODS: The basal cytotoxicity of seven compounds in Chinese hamster lung cell (CHL) cells were analyzed by MTT test, the LD50 values of acute toxicity were estimated by Registry of Cytotoxicity prediction model and validated by up-down method in mice. RESULTS: The IC50 values of compounds 1 - 7 in CHL cells were 0.43, 0.49, 0.18, 0.67, 3.03, 1.68 and 1.79 mg/mL, respectively. The predictive values of LD50 for compounds of 1 - 7 were 2376.4, 2478.3, 1574.8, 2087.6, 4897.3, 3331.8 and 3300.7 mg/kg, respectively. The LD50 values for all compounds detected by up-down method were more than 2000.0 mg/kg except compound 4 with 1634.0 mg/kg in female mice. Compared with the chemicals' toxicity classification based on predictive values and true values of LD50, the results indicated that toxicity classification of all compounds were basically at equal pace except compounds 3 and 4. CONCLUSION: The eytotoxieity data in vitro may be helpful in predicting acute toxicity in vivo and reducing the usage of laboratory animals.

关 键 词:新化学实体 急性毒性 细胞毒性 RC预测模型 

分 类 号:R965.3[医药卫生—药理学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象