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姜黄素对甲醛致A549细胞氧化损伤拮抗作用
引用本文:陈鑫,江中发,李宁,石玉琴,隋妍,张本延.姜黄素对甲醛致A549细胞氧化损伤拮抗作用[J].中国公共卫生,2012,28(4):491-492.
作者姓名:陈鑫  江中发  李宁  石玉琴  隋妍  张本延
作者单位:1. 武汉科技大学医学院预防医学系,湖北武汉,430065
2. 湖北省疾病预防控制中心
摘    要:目的探讨姜黄素对甲醛致细胞氧化损伤的拮抗效应。方法采用A549细胞株作为实验材料,实验设对照组、0.1 mmol/L甲醛染毒组,姜黄素组(0.1 mmol/L甲醛+2.5~20.0 mg/L姜黄素),检测A549细胞中一氧化氮合酶(NOS),丙二醛(MDA),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-Px)活性。结果甲醛染毒组A549细胞SOD、NOS和GSH-Px活性分别为(21.79±1.13)、(1.88±0.16)与(27.83±0.2)U/mgprot,与对照组比较,SOD、NOS和GSH-Px活性明显下降(P<0.05),MDA含量(3.87±0.153.87)nmol/mgprot]明显升高(P<0.05)。与甲醛染毒组比较,各姜黄素组GSH-Px活性上升、MDA含量下降(P<0.05),与对照组比较,40 mg/L姜黄素组GSH-Px活性、MDA含量差异无统计学意义(P>0.05)。结论姜黄素可提高A549细胞抗氧化酶活性,并存在剂量效应关系。

关 键 词:甲醛  姜黄素  氧化损伤  拮抗作用

Antagonitic effect of curcumin on formaldehyde-induced oxidative damage in A549 cell
Institution:CHEN Xin,JIANG Zhong-fa,LI Ning,et al.Department of Preventive Medicine,Medical College,Wuhan Science and Technology University(Wuhan 430065,China)
Abstract:Objective To explore the antagonistic effect of curcumin on formaldehyde-induced oxidative damage in cells.Methods A549 cells were used as experiental material and divided into normal control group,formaldehyde exposure group(0.1 mmol/L),and curcumin-antagonized formaldehyde group.Nitric oxide synthase(NOS),malondialdehyde(MDA),superoxide dismutase(SOD),and glutathione peroxidase(GSH-Px) levels were detected.Results For formaldehyde exposure group,SOD,NOS,and GSH-Px activity in A549 cells were 21.79±1.13,1.88±0.16,and 27.83±0.2 U/mgprot,respectively,and significantly decreased(P<0.05) compared to those of the control group.Compared with that of the control group,MDA increased significantly(P<0.05).Compared with the formaldehyde exposure group,GSH-Px activity increased(P<0.05),MDA content decreased in curcumine group(P<0.05).Compared with those of the control group,GSH-Px activity and MDA content showed no significant difference in 40 mg/L curcumine group(P>0.05).Conclusion Curcumin can enhance antioxidant enzyme activity in A549 cells in a dose-effect relationship.
Keywords:formaldehyde  curcumine  oxidative damage  antagonism
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