Effect of subchronic exposure to arsenic on levels of essential trace elements in mice brain and its gender difference

Biometals. 2013 Feb;26(1):123-31. doi: 10.1007/s10534-012-9599-6. Epub 2012 Dec 9.

Abstract

The interactions of toxic metals with essential metals may result in disturbances in the homeostasis of essential elements. However, there are few reports about toxic effect of arsenic (As) on the levels of essential trace elements in the central nervous system. To investigate whether subchronic exposure to As disturbs levels of main essential trace elements in the brain of mice and whether the gender difference in the response to As are altered, the concentrations of As, Iron (Fe), copper (Cu), selenium (Se), zinc (Zn) and Chromium (Cr) in the cerebrum and cerebellum of mice exposed to As subchronically were examined by inductively coupled plasma-mass spectrometry (ICP-MS). The gender difference in the changed levels of these essential trace elements was also statistically analyzed. The concentration of As was significantly higher in the cerebrum or cerebellum of mice exposed to As than that in control group (P < 0.05). It indicates that As can accumulate in brain of mice after subchronic exposure. The concentrations of Fe, Se and Cr in the cerebrum or cerebellum were significantly lower in mice exposed to As than those in control group (P < 0.05). On the contrary, the concentration of Cu in the cerebrum or cerebellum was significantly higher in mice exposed to As (P < 0.05). Our results indicate that subchronic exposure to As may decrease the levels of Fe, Se and Cr or increase the level of Cu in the brain of mice. Moreover, the significant gender difference was found relative to the effect of As on concentration of Se in cerebrum and concentrations of Cu and Se in cerebellum of mice. Therefore, more experiments are required to further understand mechanisms whereby As interacts with essential elements in brain and induces the gender difference.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arsenic Trioxide
  • Arsenicals / pharmacokinetics
  • Cerebellum / drug effects
  • Cerebellum / metabolism*
  • Cerebrum / drug effects
  • Cerebrum / metabolism*
  • Chromium / metabolism
  • Copper / metabolism
  • Environmental Pollutants / pharmacokinetics
  • Environmental Pollutants / toxicity*
  • Female
  • Iron / metabolism
  • Male
  • Mice
  • Oxides / pharmacokinetics
  • Oxides / toxicity*
  • Selenium / metabolism
  • Sex Factors
  • Tissue Distribution
  • Trace Elements / metabolism*
  • Zinc / metabolism

Substances

  • Arsenicals
  • Environmental Pollutants
  • Oxides
  • Trace Elements
  • Chromium
  • Copper
  • Iron
  • Selenium
  • Zinc
  • Arsenic Trioxide