| Literature DB >> 26257159 |
Guanghua Mao1, Zhaoxiang Zhou2, Yao Chen1, Wei Wang3, Xueshan Wu2, Weiwei Feng3, Samuel Jerry Cobbina1, Jing Huang2, Zhen Zhang1, Hai Xu1, Liuqing Yang4, Xiangyang Wu5.
Abstract
The objective of this study was to evaluate the toxicity of individual and mixtures of di(n-butyl) phthalates (DBP) and their active metabolite monobutyl phthalate (MBP) and arsenic (As) on spatial cognition associated with hippocampal apoptosis in mice. Mice were exposed, individually or in combination, to DBP (50 mg/kg body weight, intragastrically), MBP (50 mg/kg body weight, intragastrically), and As (10 mg/L, per os) for 8 weeks. The Morris water maze test showed that mice exposed to DBP/MBP combined with As exhibited longer escape latencies and the lower average number of crossing the platform. The As content in the hippocampus after As exposure increased as compared to those without As exposure. In mice exposed to DBP/MBP combined with As, pathological alterations and oxidative damage to the hippocampus were found. Expression of apoptosis-related protein: Bax and caspase-3 were significantly increased in the hippocampus, while there was no significant change in expression of Bcl-2. The results suggested that DBP and MBP combined with As can induce spatial cognitive deficits through altering the expression of apoptosis-related protein and As played a critical role in cognition impairments. And the joint exposure has antagonistic effect.Entities:
Keywords: Antagonistic effect; Arsenic; Combined neurotoxicology; Di (n-butyl) phthalate; Monobutyl phthalate
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Year: 2015 PMID: 26257159 DOI: 10.1007/s12011-015-0457-6
Source DB: PubMed Journal: Biol Trace Elem Res ISSN: 0163-4984 Impact factor: 3.738