Abstract

BackgroundArsenic is a developmental neurotoxicant. It means that its neurotoxic effect could occur in offspring by maternal arsenic exposure. Our previous study showed that developmental arsenic exposure impaired social behavior and serotonergic system in C3H adult male mice. These effects might affect the next generation with no direct exposure to arsenic. This study aimed to detect the social behavior and related gene expression changes in F2 male mice born to gestationally arsenite-exposed F1 mice.MethodsPregnant C3H/HeN mice (F0) were given free access to tap water (control mice) or tap water containing 85 ppm sodium arsenite from days 8 to 18 of gestation. Arsenite was not given to F1 or F2 mice. The F2 mice were generated by mating among control F1 males and females, and arsenite-F1 males and females at the age of 10 weeks. At 41 weeks and 74 weeks of age respectively, F2 males were used for the assessment of social behavior by a three-chamber social behavior apparatus. Histological features of the prefrontal cortex were studied by ordinary light microscope. Social behavior-related gene expressions were determined in the prefrontal cortex by real time RT-PCR method.ResultsThe arsenite-F2 male mice showed significantly poor sociability and social novelty preference in both 41-week-old group and 74-week-old group. There was no significant histological difference between the control mice and the arsenite-F2 mice. Regarding gene expression, serotonin receptor 5B (5-HT 5B) mRNA expression was significantly decreased (p < 0.05) in the arsenite-F2 male mice compared to the control F2 male mice in both groups. Brain-derived neurotrophic factor (BDNF) and dopamine receptor D1a (Drd1a) gene expressions were significantly decreased (p < 0.05) only in the arsenite-F2 male mice of the 74-week-old group. Heme oxygenase-1 (HO-1) gene expression was significantly increased (p < 0.001) in the arsenite-F2 male mice of both groups, but plasma 8-hydroxy-2′-deoxyguanosine (8-OHdG) and cyclooxygenase-2 (COX-2) gene expression were not significantly different. Interleukin-1β (IL-1β) mRNA expression was significantly increased only in 41-week-old arsenite-F2 mice.ConclusionsThese findings suggest that maternal arsenic exposure affects social behavior in F2 male mice via serotonergic system in the prefrontal cortex. In this study, COX-2 were not increased although oxidative stress marker (HO-1) was increased significantly in arsnite-F2 male mice.

Highlights

  • IntroductionOur previous study showed that developmental arsenic exposure impaired social behavior and serotonergic system in C3H adult male mice

  • We studied the mRNA expressions of 5-HT 5-hydroxytryptamine receptor 5B (5B) and Brain-derived neurotrophic factor (BDNF) in the prefrontal cortex, and these were found to be decreased in the arsenite-Second generation (F2) mice compared to the control mice

  • Social behavior is mainly concerned with the prefrontal cortex and so we studied the histological features and social behavioral-related gene expression in the prefrontal cortex

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Summary

Introduction

Our previous study showed that developmental arsenic exposure impaired social behavior and serotonergic system in C3H adult male mice. These effects might affect the generation with no direct exposure to arsenic. There are many evidences of health hazards due to drinking arsenic-contaminated water above this level for a certain period. From the evidence of animal studies, developmental arsenic exposure leads to definite health hazards in the offspring because arsenic can pass through the placenta [3]. Developmental exposure is known as maternal exposure because arsenic-contaminated water is only given to pregnant mother and not given directly to the offspring. Arsenic is never given directly to offspring, but it might reach to offspring through placenta circulation and lactation [4]

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