Investigation of the effect for bisphenol A on oxidative stress in human hepatocytes and its interaction with catalase

被引:30
|
作者
Piao, Xianmei [2 ]
Liu, Zhongrui [1 ]
Li, Yangyang [1 ]
Yao, Dahong [3 ]
Sun, Liwen [1 ]
Wang, Baihui [1 ]
Ma, Yan [1 ]
Wang, Libo [1 ]
Zhang, Yan [2 ]
机构
[1] Harbin Med Univ, Coll Pharm, Dept Med Chem & Nat Med Chem, Baojian Rd 157, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Coll Pharm, Dept Pharmacol, Key Lab Cardiovasc Med Res,Minist Educ,State Prov, Baojian Rd 157, Harbin 150081, Heilongjiang, Peoples R China
[3] Shenzhen Univ, Dept Med Chem, Coll Pharm, Nanhai Rd 3688, Shenzhen 518060, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Bisphenol A; Catalase; Oxidative stress; Hepatocyte; Spectroscopy; HUMAN SERUM-ALBUMIN; HUMAN EXPOSURE; BINDING; INFLAMMATION; FEMALE; CHINA;
D O I
10.1016/j.saa.2019.117149
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Bisphenol A (BPA) as a chemical raw material, is widely used in the manufacturing process of daily necessities. It was reported that BPA could induce oxidative stress, and catalase (CAT) can protect the body from oxidative stress. In this paper, the effect of BPA on CAT was carried out in vitro and in vivo. Firstly, we studied the effects of BPA on oxidative stress, cell viability and CAT activity in human hepatocytes, and the results of vitro experiments show that the survival rate of hepatocytes significant decreased along with the increase of BPA concentration. And when the BPA concentration was 100 mu M, the hepatocyte survival decreased by 13.2%, ROS levels in the cells increased by 85%. However, the activity of intracellular CAT increased with the increasing concentration of BPA in 24 h. The results of vivo experiments showed that the activity of CAT in the high-dose group decreased by 29.1% compared with the control group. The long-term effects of BPA on rats reduced the CAT activity in liver, which reduced the resistance to oxidative stress. Meanwhile, the interaction mechanism between BPA and CAT at the molecule level was performed via multiple spectra methods and molecular docking, and the results illustrated that the structural change of CAT is mainly due to the strong combination of BPA with the residues of Trp185. In addition, the interaction mechanism between BPA and CAT were hydrophobic and electrostatic effect. This study provided experimental evidence for better understanding the toxicity of BPA. (C) 2019 Elsevier B.V. All rights reserved.
引用
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页数:8
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