Zinc and imipramine reverse the depression-like behavior in mice induced by chronic restraint stress

Abstract Depression is a common psychopathological disorders. Studies of depression have indicated that zinc play a role in the depression pathophysiology and treatment. In present study, we examined the effects of zinc and imipramine supplement alone or combination of zinc and imipramine in mice in...

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Veröffentlicht in:Journal of affective disorders 2016-06, Vol.197, p.100-106
Hauptverfasser: Ding, Qin, Li, Hongxia, Tian, Xue, Shen, Zhilei, Wang, Xiaoli, Mo, Fengfeng, Huang, Junlong, Shen, Hui
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container_start_page 100
container_title Journal of affective disorders
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creator Ding, Qin
Li, Hongxia
Tian, Xue
Shen, Zhilei
Wang, Xiaoli
Mo, Fengfeng
Huang, Junlong
Shen, Hui
description Abstract Depression is a common psychopathological disorders. Studies of depression have indicated that zinc play a role in the depression pathophysiology and treatment. In present study, we examined the effects of zinc and imipramine supplement alone or combination of zinc and imipramine in mice induced by chronic restraint stress (CRS). Moreover, the possible roles of zinc receptor (G protein-coupled receptor 39, GPR39)-related pathway was investigated. Decreased weight and increased corticosterone (CORT) were observed after 3 weeks CRS exposure. It was shown that CRS induced lower serum zinc, higher hippocampal zinc, increased immobility time in tail suspension test and decreased movement distance in spontaneous activity test, which could be normalized by zinc (30 mg/kg) and imipramine (20 mg/kg) supplement alone and combination of zinc (15 mg/kg) and imipramine (5 mg/kg) for 3 weeks after CRS exposure. Moreover, the changes in mRNA expressions of GPR39, cAMP-response element binding protein (CREB), brain-derived neurotropic factor (BDNF) and n-methytl- d -aspartate receptors (NMDAR) could be reversed by the same treatment mentioned above. These results suggested that zinc dyshomeostasis in serum and hippocampus and depression-like behavior in CRS exposure animals observed in present study could be normalized by zinc and imipramine. The combination of zinc and imipramine in low dose has synergetic effects. The possible mechanism might be correlated to GPR39 receptor-related pathway.
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Moreover, the changes in mRNA expressions of GPR39, cAMP-response element binding protein (CREB), brain-derived neurotropic factor (BDNF) and n-methytl- d -aspartate receptors (NMDAR) could be reversed by the same treatment mentioned above. These results suggested that zinc dyshomeostasis in serum and hippocampus and depression-like behavior in CRS exposure animals observed in present study could be normalized by zinc and imipramine. The combination of zinc and imipramine in low dose has synergetic effects. 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Studies of depression have indicated that zinc play a role in the depression pathophysiology and treatment. In present study, we examined the effects of zinc and imipramine supplement alone or combination of zinc and imipramine in mice induced by chronic restraint stress (CRS). Moreover, the possible roles of zinc receptor (G protein-coupled receptor 39, GPR39)-related pathway was investigated. Decreased weight and increased corticosterone (CORT) were observed after 3 weeks CRS exposure. It was shown that CRS induced lower serum zinc, higher hippocampal zinc, increased immobility time in tail suspension test and decreased movement distance in spontaneous activity test, which could be normalized by zinc (30 mg/kg) and imipramine (20 mg/kg) supplement alone and combination of zinc (15 mg/kg) and imipramine (5 mg/kg) for 3 weeks after CRS exposure. Moreover, the changes in mRNA expressions of GPR39, cAMP-response element binding protein (CREB), brain-derived neurotropic factor (BDNF) and n-methytl- d -aspartate receptors (NMDAR) could be reversed by the same treatment mentioned above. These results suggested that zinc dyshomeostasis in serum and hippocampus and depression-like behavior in CRS exposure animals observed in present study could be normalized by zinc and imipramine. The combination of zinc and imipramine in low dose has synergetic effects. The possible mechanism might be correlated to GPR39 receptor-related pathway.</description><subject>Animals</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Chronic restraint stress</subject><subject>Corticosterone - blood</subject><subject>CREB-Binding Protein - metabolism</subject><subject>Depression</subject><subject>Depression - blood</subject><subject>Depression - drug therapy</subject><subject>Depression - etiology</subject><subject>Depression - metabolism</subject><subject>Depressive Disorder - blood</subject><subject>Depressive Disorder - drug therapy</subject><subject>Depressive Disorder - etiology</subject><subject>Depressive Disorder - metabolism</subject><subject>Drug Synergism</subject><subject>GPR39</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Imipramine</subject><subject>Imipramine - pharmacology</subject><subject>Imipramine - therapeutic use</subject><subject>Male</subject><subject>Mice</subject><subject>Psychiatry</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Restraint, Physical - psychology</subject><subject>Signal Transduction - drug effects</subject><subject>Stress, Psychological - etiology</subject><subject>Stress, Psychological - psychology</subject><subject>Zinc</subject><subject>Zinc - pharmacology</subject><subject>Zinc - therapeutic use</subject><issn>0165-0327</issn><issn>1573-2517</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk2r1DAUDaL4xqc_wI1k6ab13qRtWgRBHn7BAxfqxk1IkztM-tp0TNqB-fcvZZ4uXOjqBO4554ZzLmMvEUoEbN4M5WBcKfKzBFkCqkdsh7WShahRPWa7PKgLkEJdsWcpDQDQdAqesivRdG2tKtwx99MHy01w3E_-GM3kA_FIJ4qJ-HIg7ugYKSU_h2L0d8R7OpiTnyP3gU_eUka3WnK8P3N7iHPwNuvTEo0PC8-Yxc_Zk70ZE714wGv24-OH7zefi9uvn77cvL8tbFXhUjQoewkVyc60ZGVnewCLyvS2Fa00yjRuLxrR2a6SNZpaGlfXykCr9tiBqOQ1e33xPcb515o_oSefLI2jCTSvSWMLbaNEhe3_qWrbCVUnMxUvVBvnlCLt9TH6ycSzRtBbD3rQuQe99aBB6txD1rx6sF_7idwfxe_gM-HthUA5j5OnqJP1FHKQPpJdtJv9P-3f_aW2o8_Jm_GOzpSGeY0hB61RJ6FBf9sOYbsDrCUKrKS8BxHorN8</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Ding, Qin</creator><creator>Li, Hongxia</creator><creator>Tian, Xue</creator><creator>Shen, Zhilei</creator><creator>Wang, Xiaoli</creator><creator>Mo, Fengfeng</creator><creator>Huang, Junlong</creator><creator>Shen, Hui</creator><general>Elsevier B.V</general><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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20160601</creationdate><title>Zinc and imipramine reverse the depression-like behavior in mice induced by chronic restraint stress</title><author>Ding, Qin ; Li, Hongxia ; Tian, Xue ; Shen, Zhilei ; Wang, Xiaoli ; Mo, Fengfeng ; Huang, Junlong ; Shen, Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-613b304e39a8ec39cb00c17abc8283a7a6df2629c94351a53ad557a087f190243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Chronic restraint stress</topic><topic>Corticosterone - blood</topic><topic>CREB-Binding Protein - metabolism</topic><topic>Depression</topic><topic>Depression - blood</topic><topic>Depression - drug therapy</topic><topic>Depression - etiology</topic><topic>Depression - metabolism</topic><topic>Depressive Disorder - blood</topic><topic>Depressive Disorder - drug therapy</topic><topic>Depressive Disorder - etiology</topic><topic>Depressive Disorder - metabolism</topic><topic>Drug Synergism</topic><topic>GPR39</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Imipramine</topic><topic>Imipramine - pharmacology</topic><topic>Imipramine - therapeutic use</topic><topic>Male</topic><topic>Mice</topic><topic>Psychiatry</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Restraint, Physical - psychology</topic><topic>Signal Transduction - drug effects</topic><topic>Stress, Psychological - etiology</topic><topic>Stress, Psychological - psychology</topic><topic>Zinc</topic><topic>Zinc - pharmacology</topic><topic>Zinc - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Qin</creatorcontrib><creatorcontrib>Li, Hongxia</creatorcontrib><creatorcontrib>Tian, Xue</creatorcontrib><creatorcontrib>Shen, Zhilei</creatorcontrib><creatorcontrib>Wang, Xiaoli</creatorcontrib><creatorcontrib>Mo, Fengfeng</creatorcontrib><creatorcontrib>Huang, Junlong</creatorcontrib><creatorcontrib>Shen, Hui</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of affective disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Qin</au><au>Li, Hongxia</au><au>Tian, Xue</au><au>Shen, Zhilei</au><au>Wang, Xiaoli</au><au>Mo, Fengfeng</au><au>Huang, Junlong</au><au>Shen, Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zinc and imipramine reverse the depression-like behavior in mice induced by chronic restraint stress</atitle><jtitle>Journal of affective disorders</jtitle><addtitle>J Affect Disord</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>197</volume><spage>100</spage><epage>106</epage><pages>100-106</pages><issn>0165-0327</issn><eissn>1573-2517</eissn><abstract>Abstract Depression is a common psychopathological disorders. 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Moreover, the changes in mRNA expressions of GPR39, cAMP-response element binding protein (CREB), brain-derived neurotropic factor (BDNF) and n-methytl- d -aspartate receptors (NMDAR) could be reversed by the same treatment mentioned above. These results suggested that zinc dyshomeostasis in serum and hippocampus and depression-like behavior in CRS exposure animals observed in present study could be normalized by zinc and imipramine. The combination of zinc and imipramine in low dose has synergetic effects. The possible mechanism might be correlated to GPR39 receptor-related pathway.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26985741</pmid><doi>10.1016/j.jad.2016.03.017</doi><tpages>7</tpages></addata></record>
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subjects Animals
Brain-Derived Neurotrophic Factor - metabolism
Chronic restraint stress
Corticosterone - blood
CREB-Binding Protein - metabolism
Depression
Depression - blood
Depression - drug therapy
Depression - etiology
Depression - metabolism
Depressive Disorder - blood
Depressive Disorder - drug therapy
Depressive Disorder - etiology
Depressive Disorder - metabolism
Drug Synergism
GPR39
Hippocampus - drug effects
Hippocampus - metabolism
Imipramine
Imipramine - pharmacology
Imipramine - therapeutic use
Male
Mice
Psychiatry
Receptors, G-Protein-Coupled - metabolism
Receptors, N-Methyl-D-Aspartate - metabolism
Restraint, Physical - psychology
Signal Transduction - drug effects
Stress, Psychological - etiology
Stress, Psychological - psychology
Zinc
Zinc - pharmacology
Zinc - therapeutic use
title Zinc and imipramine reverse the depression-like behavior in mice induced by chronic restraint stress
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