Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression

Accumulating evidence implicates that subchronic arsenic exposure causes cerebral neurodegeneration leading to behavioral disturbances relevant to psychiatric disorders. However, there is still little information regarding the influence of subchronic exposure to arsenic-contaminated drinking water o...

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Veröffentlicht in:BioMed research international 2015-01, Vol.2015 (2015), p.1-12
Hauptverfasser: Chuu, Jiunn-Jye, Lin, Li-Chuan, Yang, Kai-Lin, Tsai, Wan-Chen, Guo, How-Ran, Chang, Chia-Yu, Cheng, Tain-Junn
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container_issue 2015
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container_title BioMed research international
container_volume 2015
creator Chuu, Jiunn-Jye
Lin, Li-Chuan
Yang, Kai-Lin
Tsai, Wan-Chen
Guo, How-Ran
Chang, Chia-Yu
Cheng, Tain-Junn
description Accumulating evidence implicates that subchronic arsenic exposure causes cerebral neurodegeneration leading to behavioral disturbances relevant to psychiatric disorders. However, there is still little information regarding the influence of subchronic exposure to arsenic-contaminated drinking water on mood disorders and its underlying mechanisms in the cerebral prefrontal cortex. The aim of this study is to assess the effects of subchronic arsenic exposure (10 mg/LAs2O3 in drinking water) on the anxiety- and depression-like behaviors in normal mice and in the chemically induced mouse model of depression by reserpine pretreatment. Our findings demonstrated that 4 weeks of arsenic exposure enhance anxiety-like behaviors on elevated plus maze (EPM) and open field test (OFT) in normal mice, and 8 weeks of arsenic exposure augment depression-like behaviors on tail suspension test (TST) and forced swimming test (FST) in the reserpine pretreated mice. In summary, in this present study, we demonstrated that subchronic arsenic exposure induces only the anxiety-like behaviors in normal mice and enhances the depression-like behaviors in the reserpine induced mouse model of depression, in which the cerebral prefrontal cortex BDNF-TrkB signaling pathway is involved. We also found that eight weeks of subchronic arsenic exposure are needed to enhance the depression-like behaviors in the mouse model of depression. These findings imply that arsenic could be an enhancer of depressive symptoms for those patients who already had the attribute of depression.
doi_str_mv 10.1155/2015/159015
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However, there is still little information regarding the influence of subchronic exposure to arsenic-contaminated drinking water on mood disorders and its underlying mechanisms in the cerebral prefrontal cortex. The aim of this study is to assess the effects of subchronic arsenic exposure (10 mg/LAs2O3 in drinking water) on the anxiety- and depression-like behaviors in normal mice and in the chemically induced mouse model of depression by reserpine pretreatment. Our findings demonstrated that 4 weeks of arsenic exposure enhance anxiety-like behaviors on elevated plus maze (EPM) and open field test (OFT) in normal mice, and 8 weeks of arsenic exposure augment depression-like behaviors on tail suspension test (TST) and forced swimming test (FST) in the reserpine pretreated mice. In summary, in this present study, we demonstrated that subchronic arsenic exposure induces only the anxiety-like behaviors in normal mice and enhances the depression-like behaviors in the reserpine induced mouse model of depression, in which the cerebral prefrontal cortex BDNF-TrkB signaling pathway is involved. We also found that eight weeks of subchronic arsenic exposure are needed to enhance the depression-like behaviors in the mouse model of depression. These findings imply that arsenic could be an enhancer of depressive symptoms for those patients who already had the attribute of depression.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2015/159015</identifier><identifier>PMID: 26114099</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Anxiety ; Anxiety - chemically induced ; Anxiety - metabolism ; Anxiety - physiopathology ; Arsenic ; Arsenic - toxicity ; Behavior, Animal - drug effects ; Behavior, Animal - physiology ; Brain-Derived Neurotrophic Factor - metabolism ; Depression, Mental ; Depressive Disorder - chemically induced ; Depressive Disorder - metabolism ; Depressive Disorder - physiopathology ; Disease Models, Animal ; Drinking water ; Health aspects ; Humans ; Kinases ; Mice ; Physiological aspects ; Prefrontal Cortex - metabolism ; Prefrontal Cortex - physiopathology ; Receptor, trkB - metabolism ; Stress, Psychological ; Studies ; Swimming</subject><ispartof>BioMed research international, 2015-01, Vol.2015 (2015), p.1-12</ispartof><rights>Copyright © 2015 Chia-Yu Chang et al.</rights><rights>COPYRIGHT 2015 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2015 Chia-Yu Chang et al. 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However, there is still little information regarding the influence of subchronic exposure to arsenic-contaminated drinking water on mood disorders and its underlying mechanisms in the cerebral prefrontal cortex. The aim of this study is to assess the effects of subchronic arsenic exposure (10 mg/LAs2O3 in drinking water) on the anxiety- and depression-like behaviors in normal mice and in the chemically induced mouse model of depression by reserpine pretreatment. Our findings demonstrated that 4 weeks of arsenic exposure enhance anxiety-like behaviors on elevated plus maze (EPM) and open field test (OFT) in normal mice, and 8 weeks of arsenic exposure augment depression-like behaviors on tail suspension test (TST) and forced swimming test (FST) in the reserpine pretreated mice. 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subjects Animals
Anxiety
Anxiety - chemically induced
Anxiety - metabolism
Anxiety - physiopathology
Arsenic
Arsenic - toxicity
Behavior, Animal - drug effects
Behavior, Animal - physiology
Brain-Derived Neurotrophic Factor - metabolism
Depression, Mental
Depressive Disorder - chemically induced
Depressive Disorder - metabolism
Depressive Disorder - physiopathology
Disease Models, Animal
Drinking water
Health aspects
Humans
Kinases
Mice
Physiological aspects
Prefrontal Cortex - metabolism
Prefrontal Cortex - physiopathology
Receptor, trkB - metabolism
Stress, Psychological
Studies
Swimming
title Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression
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