Adverse effect of sub-chronic exposure to benzo(a)pyrene and protective effect of butylated hydroxyanisole on learning and memory ability in male Sprague-Dawley rat

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Author(s)

    • Liang Xiao Liang Xiao
    • Department of Occupational and Environmental Medicine, School of Public Health, Chongqing Medical University
    • Tang Yan Tang Yan
    • Department of Occupational and Environmental Medicine, School of Public Health, Luzhou Medical College
    • Duan Li [他] Duan Li
    • Department of Occupational and Environmental Medicine, School of Public Health, Chongqing Medical University
    • Cheng Shuqun
    • Department of Occupational and Environmental Medicine, School of Public Health, Chongqing Medical University
    • Luo Long
    • Department of Occupational and Environmental Medicine, School of Public Health, Chongqing Medical University
    • Cao Xianqing
    • Experiment center, School of Public Health, Chongqing Medical University
    • Tu Baijie
    • Department of Occupational and Environmental Medicine, School of Public Health, Chongqing Medical University

Abstract

Previous studies demonstrate that benzo(a)pyrene (B(a)P) can affect hippocampal function and cause spatial cognition impairment. However, the mechanism is incomplete. Some evidence implies that B(a)P may cause an oxidative damage linking to the function of the hippocampus and antioxidant can prevent the oxidative damage in rats, but the ATPase and Ca<sup>2+</sup> in the hippocampus and the protective effect of butylated hydroxyanisole (BHA) have not been studied. This study aimed to investigate the damage of toxicity further induced by B(a)P in hippocampus and the protective effect of BHA. Ninety-six male Sprague-Dawley (SD) rats were randomly divided into four groups (solvent control group, BHA-group, B(a)P-exposed group and B(a)P-BHA-combination group), with daily administration for 90days. Morris water maze (MWM) was employed to evaluate the learning and memory ability. The levels of malonaldehyde (MDA) content, superoxide dismutase (SOD) activity, Na<sup>+</sup>-K<sup>+</sup>-ATPase and Ca<sup>2+</sup>-Mg<sup>2+</sup>ATPase activity in hippocampus were measured by commercial kits. The concentration of Ca<sup>2+ </sup>in rat hippocampus was detected by fluorescent labeling. In behavior test it showed that there was an adverse effect on rats in the B(a)P -group. The levels of MDA content and Ca<sup>2+</sup> content were significantly increased in the B(a)P group, while the activities of SOD and ATPase were significantly decreased. In the B(a)P-BHA group, the change of each index diminished significantly. The results suggested that the neurobehavioral toxicity of B(a)P might have a close relationship with oxidative damage, resulted in decreasing of ATPase activities and increasing of Ca<sup>2+</sup> concentration in the hippocampus. Furthermore, BHA can prevent these damages.

Journal

  • The Journal of Toxicological Sciences

    The Journal of Toxicological Sciences 39(5), 739-748, 2014

    The Japanese Society of Toxicology

Codes

  • NII Article ID (NAID)
    130004690961
  • NII NACSIS-CAT ID (NCID)
    AN00002808
  • Text Lang
    ENG
  • ISSN
    0388-1350
  • NDL Article ID
    025850946
  • NDL Call No.
    Z19-1022
  • Data Source
    NDL  J-STAGE 
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