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...
Gespeichert in:
Veröffentlicht in: | BioMed research international 2015-01, Vol.2015 (2015), p.1-12 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 12 |
---|---|
container_issue | 2015 |
container_start_page | 1 |
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 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4465655</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A458160319</galeid><sourcerecordid>A458160319</sourcerecordid><originalsourceid>FETCH-LOGICAL-c594t-8718d8b50c6dfb97102f982c97e65d5ca36f320d1f36711a1398c89edd667a723</originalsourceid><addsrcrecordid>eNqNkstuEzEUhkcIRKvSFXtkiQ0Chdrj8W2DFEKASiksgLXl2Gc6LhM7tTOleR8eFI9SQkBI4IWPJX_-fS5_VT0m-CUhjJ3VmLAzwlQJ96rjmpJmwklD7u_PlB5Vpzlf4bIk4Vjxh9VRzQlpsFLH1fdPw9J2KQZv0TRlGOP8dh3zkACdBzdYyGgabj1stpOF_wroNXTmxseUkQ_oQ0wr06MLbwGZ4NA8dCaMT97AOkHOPoa_vNp0gGYdrLw1fb-9-8ahizhkKLuDHsX2QOJR9aA1fYbTu3hSfXk7_zx7P1l8fHc-my4mlqlmM5GCSCeXDFvu2qUSBNetkrVVAjhzzBrKW1pjR1rKBSGGUCWtVOAc58KImp5Ur3a662G5AmchbJLp9Tr5lUlbHY3Xv98E3-nLeKObhjPOWBF4dieQ4vUAeaNXPlvoexOgFKeJKHPCWCj5b5SrMlYp5JjW0z_QqzikUDpRKCkU45iKX9Sl6UH70MaSoh1F9bRh4-gpUYV6saNsijknaPfVEaxHR-nRUXrnqEI_OWzInv3pnwI83wGdD8588_-nBgWB1hzArGkIoT8ASWncaQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1687956037</pqid></control><display><type>article</type><title>Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression</title><source>MEDLINE</source><source>PubMed Central Open Access</source><source>Wiley-Blackwell Open Access Titles</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Chuu, Jiunn-Jye ; Lin, Li-Chuan ; Yang, Kai-Lin ; Tsai, Wan-Chen ; Guo, How-Ran ; Chang, Chia-Yu ; Cheng, Tain-Junn</creator><contributor>de Sousa, Damião Pergentino</contributor><creatorcontrib>Chuu, Jiunn-Jye ; Lin, Li-Chuan ; Yang, Kai-Lin ; Tsai, Wan-Chen ; Guo, How-Ran ; Chang, Chia-Yu ; Cheng, Tain-Junn ; de Sousa, Damião Pergentino</creatorcontrib><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.</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 & Sons, Inc.</rights><rights>Copyright © 2015 Chia-Yu Chang et al. Chia-Yu Chang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2015 Chia-Yu Chang et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-8718d8b50c6dfb97102f982c97e65d5ca36f320d1f36711a1398c89edd667a723</citedby><cites>FETCH-LOGICAL-c594t-8718d8b50c6dfb97102f982c97e65d5ca36f320d1f36711a1398c89edd667a723</cites><orcidid>0000-0003-1289-8412 ; 0000-0002-8332-3993</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465655/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465655/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26114099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>de Sousa, Damião Pergentino</contributor><creatorcontrib>Chuu, Jiunn-Jye</creatorcontrib><creatorcontrib>Lin, Li-Chuan</creatorcontrib><creatorcontrib>Yang, Kai-Lin</creatorcontrib><creatorcontrib>Tsai, Wan-Chen</creatorcontrib><creatorcontrib>Guo, How-Ran</creatorcontrib><creatorcontrib>Chang, Chia-Yu</creatorcontrib><creatorcontrib>Cheng, Tain-Junn</creatorcontrib><title>Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><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.</description><subject>Animals</subject><subject>Anxiety</subject><subject>Anxiety - chemically induced</subject><subject>Anxiety - metabolism</subject><subject>Anxiety - physiopathology</subject><subject>Arsenic</subject><subject>Arsenic - toxicity</subject><subject>Behavior, Animal - drug effects</subject><subject>Behavior, Animal - physiology</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Depression, Mental</subject><subject>Depressive Disorder - chemically induced</subject><subject>Depressive Disorder - metabolism</subject><subject>Depressive Disorder - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Drinking water</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Kinases</subject><subject>Mice</subject><subject>Physiological aspects</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Receptor, trkB - metabolism</subject><subject>Stress, Psychological</subject><subject>Studies</subject><subject>Swimming</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkstuEzEUhkcIRKvSFXtkiQ0Chdrj8W2DFEKASiksgLXl2Gc6LhM7tTOleR8eFI9SQkBI4IWPJX_-fS5_VT0m-CUhjJ3VmLAzwlQJ96rjmpJmwklD7u_PlB5Vpzlf4bIk4Vjxh9VRzQlpsFLH1fdPw9J2KQZv0TRlGOP8dh3zkACdBzdYyGgabj1stpOF_wroNXTmxseUkQ_oQ0wr06MLbwGZ4NA8dCaMT97AOkHOPoa_vNp0gGYdrLw1fb-9-8ahizhkKLuDHsX2QOJR9aA1fYbTu3hSfXk7_zx7P1l8fHc-my4mlqlmM5GCSCeXDFvu2qUSBNetkrVVAjhzzBrKW1pjR1rKBSGGUCWtVOAc58KImp5Ur3a662G5AmchbJLp9Tr5lUlbHY3Xv98E3-nLeKObhjPOWBF4dieQ4vUAeaNXPlvoexOgFKeJKHPCWCj5b5SrMlYp5JjW0z_QqzikUDpRKCkU45iKX9Sl6UH70MaSoh1F9bRh4-gpUYV6saNsijknaPfVEaxHR-nRUXrnqEI_OWzInv3pnwI83wGdD8588_-nBgWB1hzArGkIoT8ASWncaQ</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Chuu, Jiunn-Jye</creator><creator>Lin, Li-Chuan</creator><creator>Yang, Kai-Lin</creator><creator>Tsai, Wan-Chen</creator><creator>Guo, How-Ran</creator><creator>Chang, Chia-Yu</creator><creator>Cheng, Tain-Junn</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1289-8412</orcidid><orcidid>https://orcid.org/0000-0002-8332-3993</orcidid></search><sort><creationdate>20150101</creationdate><title>Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression</title><author>Chuu, Jiunn-Jye ; Lin, Li-Chuan ; Yang, Kai-Lin ; Tsai, Wan-Chen ; Guo, How-Ran ; Chang, Chia-Yu ; Cheng, Tain-Junn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-8718d8b50c6dfb97102f982c97e65d5ca36f320d1f36711a1398c89edd667a723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Anxiety</topic><topic>Anxiety - chemically induced</topic><topic>Anxiety - metabolism</topic><topic>Anxiety - physiopathology</topic><topic>Arsenic</topic><topic>Arsenic - toxicity</topic><topic>Behavior, Animal - drug effects</topic><topic>Behavior, Animal - physiology</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Depression, Mental</topic><topic>Depressive Disorder - chemically induced</topic><topic>Depressive Disorder - metabolism</topic><topic>Depressive Disorder - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Drinking water</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Kinases</topic><topic>Mice</topic><topic>Physiological aspects</topic><topic>Prefrontal Cortex - metabolism</topic><topic>Prefrontal Cortex - physiopathology</topic><topic>Receptor, trkB - metabolism</topic><topic>Stress, Psychological</topic><topic>Studies</topic><topic>Swimming</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chuu, Jiunn-Jye</creatorcontrib><creatorcontrib>Lin, Li-Chuan</creatorcontrib><creatorcontrib>Yang, Kai-Lin</creatorcontrib><creatorcontrib>Tsai, Wan-Chen</creatorcontrib><creatorcontrib>Guo, How-Ran</creatorcontrib><creatorcontrib>Chang, Chia-Yu</creatorcontrib><creatorcontrib>Cheng, Tain-Junn</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chuu, Jiunn-Jye</au><au>Lin, Li-Chuan</au><au>Yang, Kai-Lin</au><au>Tsai, Wan-Chen</au><au>Guo, How-Ran</au><au>Chang, Chia-Yu</au><au>Cheng, Tain-Junn</au><au>de Sousa, Damião Pergentino</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subchronic Arsenic Exposure Induces Anxiety-Like Behaviors in Normal Mice and Enhances Depression-Like Behaviors in the Chemically Induced Mouse Model of Depression</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>2015</volume><issue>2015</issue><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>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.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>26114099</pmid><doi>10.1155/2015/159015</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-1289-8412</orcidid><orcidid>https://orcid.org/0000-0002-8332-3993</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-6133 |
ispartof | BioMed research international, 2015-01, Vol.2015 (2015), p.1-12 |
issn | 2314-6133 2314-6141 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4465655 |
source | MEDLINE; PubMed Central Open Access; Wiley-Blackwell Open Access Titles; PubMed Central; Alma/SFX Local Collection |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T04%3A00%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Subchronic%20Arsenic%20Exposure%20Induces%20Anxiety-Like%20Behaviors%20in%20Normal%20Mice%20and%20Enhances%20Depression-Like%20Behaviors%20in%20the%20Chemically%20Induced%20Mouse%20Model%20of%20Depression&rft.jtitle=BioMed%20research%20international&rft.au=Chuu,%20Jiunn-Jye&rft.date=2015-01-01&rft.volume=2015&rft.issue=2015&rft.spage=1&rft.epage=12&rft.pages=1-12&rft.issn=2314-6133&rft.eissn=2314-6141&rft_id=info:doi/10.1155/2015/159015&rft_dat=%3Cgale_pubme%3EA458160319%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1687956037&rft_id=info:pmid/26114099&rft_galeid=A458160319&rfr_iscdi=true |