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引用本文:陈莹蓉,王翔,闵丽姗,戴利成,杨水新.黄药子醇提物Caco-2细胞摄取液对HL-7702和HepG2细胞毒性研究[J].中国现代应用药学,2013,30(4):368-372.
CHEN Yingrong,WANG Xiang,MIN Lishan,DAI Licheng,YANG Shuixin.Toxicity Study of the Uptaking Compositions of Diosooroa Bulbifera L Alcohol Extract on HL-7702 and HepG2 Cell[J].Chin J Mod Appl Pharm(中国现代应用药学),2013,30(4):368-372.
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黄药子醇提物Caco-2细胞摄取液对HL-7702和HepG2细胞毒性研究
陈莹蓉1, 王翔1, 闵丽姗1, 戴利成1, 杨水新2
1.湖州市中心医院中心实验室,湖州市分子医学重点实验室,浙江 湖州 313000;2.湖州市中心医院临床药理科,浙江 湖州 313000
摘要:
目的 研究黄药子醇提物Caco-2细胞摄取液对HL-7702和HepG2细胞的毒性。方法 75%乙醇回流提取得黄药子提取物,高、中、低剂量作用于Caco-2细胞,以黄药子醇提物Caco-2细胞摄取液作用于HL-7702和HepG2细胞,进行细胞活性实验,测定生化指标ALT、AST、GSH-PX和MDA值。结果 与对照组比,高剂量组和中剂量组黄药子醇提物Caco-2细胞摄取液作用后,HL-7702和HepG2细胞的存活率显著降低(P<0.01);高剂量组黄药子醇提物Caco-2细胞摄取液作用72 h后,HL-7702细胞上清液中ALT、AST显著升高(P<0.01);高剂量组黄药子醇提物Caco-2细胞摄取液作用48 h和72 h后,HepG2细胞上清液中ALT、AST显著升高(P<0.01)。高剂量组和中剂量组黄药子醇提物Caco-2细胞摄取液作用48 h和72 h后,HL-7702和HepG2细胞上清液中MDA显著升高,GSH-PX显著降低(P<0.01)。结论 黄药子醇提物Caco-2细胞摄取液对HL-7702和HepG2细胞有毒性。
关键词:  黄药子  Caco-2细胞  肝细胞  毒性
DOI:
分类号:
基金项目:2011年湖州市科技局一般科研计划项目(2011YS02)
Toxicity Study of the Uptaking Compositions of Diosooroa Bulbifera L Alcohol Extract on HL-7702 and HepG2 Cell
CHEN Yingrong1, WANG Xiang1, MIN Lishan1, DAI Licheng1, YANG Shuixin2
1.Laboratory, Huzhou Central Hospital, Huzhou Key Laboratory of Molecular Medicine, Huzhou 313000, China;2.Department of Clinical Pharmacology, Huzhou Central Hospital, Huzhou 313000, China
Abstract:
OBJECTIVE To study the toxicity of the uptaking compositions of Diosooroa bulbifera L alcohol extract on HL-7702 and HepG2 cell. METHODS After reflux extraction with 75% alcohol, the alcohol extracts of Diosooroa bulbifera L at high, middle and low doses were added to Caco-2 cell model. Then the uptaking compositions were added to HL-7702 and HepG2 cell for the determination of the cytoactive and the biochemical indicator of ALT, AST, GSH-PX and MDA. RESULTS Compared with the control group, the high and middle dose groups decreased the survival rate of HL-7702 and HepG2 cell (P<0.01). The high dose group increased ALT and AST of HL-7702 cell supernatant after 72 h (P<0.01). The high dose group increased ALT and AST of HepG2 cell supernatant after 48 h and 72 h (P<0.01). MDA were significant increased and GSH-PX were significant decreased in the supernatant of HL-7702 and HepG2 cell at high and middle doses after 48 h and 72 h (P<0.01). CONCLUSION The result showed that the uptaking compositions of Diosooroa bulbifera L alcohol extract had toxic effect in HL-7702 and HepG2 cell.
Key words:  Diosooroa bulbifera L  Caco-2 cell  hepatocyte  toxicity
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