Tris-(2,3-dibromopropyl) isocyanurate induces depression-like behaviors and neurotoxicity by oxidative damage and cell apoptosis in vitro and in vivo

被引:14
作者
Dong, Zhaoju [1 ]
Hu, Zhengping [3 ]
Zhu, Haibo [1 ,2 ]
Li, Ning [1 ]
Zhao, Huijuan [1 ]
Mi, Wei [1 ]
Jiang, Wanglin [4 ]
Hu, Xihou [1 ]
Ye, Liang [1 ,2 ]
机构
[1] Binzhou Med Univ, Sch Publ Hlth & Management, Yantai 264003, Shandong, Peoples R China
[2] Binzhou Med Univ, Inst Toxicol, Yantai 264003, Shandong, Peoples R China
[3] Binzhou Med Univ, Med & Pharm Res Ctr, Yantai 264003, Shandong, Peoples R China
[4] Binzhou Med Univ, Sch Pharm, Yantai 264003, Shandong, Peoples R China
关键词
Tris-(2,3-dibromopropyl) isocyanurate (TDBP-TAZTO); Depression; Hippocampus; Oxidative stress; Apoptosis; BROMINATED FLAME-RETARDANT; TRIS(2,3-DIBROMOPROPYL) ISOCYANURATE; MICE; HEXABROMOCYCLODODECANES; EXTRACT; STRESS;
D O I
10.2131/jts.40.701
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Tris-(2,3-dibromopropyl) isocyanurate (TDBP-TAZTO), an emerging brominated flame retardant, possesses the characteristics of candidate persistent organic pollutants and has displayed toxicity to fish and rodents. TDBP-TAZTO can pass through the blood-brain barrier and accumulate in the brain. TDBP-TAZTO might also induce neuronal cell toxicity. However, the neurotoxicity and mechanisms of TDBP-TAZTO have not yet been studied. We hypothesize that TDBP-TAZTO could induce neurotoxicity in mouse hippocampal neurons and SH-SY5Y cells. The mice were exposed to TDBP-TAZTO of 5 and 50 mg/kg by gavage, daily for 30 days. TDBP-TAZTO resulted in depression-like behaviors, which may be related with TDBP-TAZTO-induced upregulation of oxidative stress markers and overexpression of pro-apoptotic proteins in hippocampus. Furthermore, TDBP-TAZTO treatment for 48 hr (12.5, 25 and 50 mu M) damaged SH-SY5Y cells, and led to cell apoptosis and oxidative stress in concentration-dependent manner. Our findings suggested that cell apoptosis and oxidative stress are important mechanisms in neurotoxicity induced by TDBP-TAZTO.
引用
收藏
页码:701 / 709
页数:9
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