DNA methylation of the Tacr2 gene in a CUMS model of depression
•We measured the changes of Tacr2 expression in the hypothalamus of CUMS-sensitive rats.•Stress may change the DNA methylation levels of the CpG island in Tacr2 promoter region.•Tacr2 expression of CUMS-sensitive rats may correlated with the DNA methylation of Tacr2 gene.. Tacr2, the gene encoding t...
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description | •We measured the changes of Tacr2 expression in the hypothalamus of CUMS-sensitive rats.•Stress may change the DNA methylation levels of the CpG island in Tacr2 promoter region.•Tacr2 expression of CUMS-sensitive rats may correlated with the DNA methylation of Tacr2 gene..
Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional processes. However, the extent, to which stress impacts Tacr2 expression remains unclear. The molecular mechanisms underlying depression also remain poorly understood. In this study, we subjected adult male Sprague Dawley (SD) rats to chronic unpredictable mild stress (CUMS) to induce a depression-like phenotype. We then measured the body weight and performed the sucrose preference test, forced swimming test (FST) and open field test to detect the effects of stress on anhedonia and activity. Western blotting and real-time PCR were used to study the protein and mRNA expression levels of Tacr2, respectively, in the hypothalamus. To explore DNA methylation of the Tacr2 gene, we used methylated DNA immunoprecipitation sequencing (MeDIP-seq). Additionally, we used the bisulfite sequencing PCR (BSP) to further verify the DNA methylation levels of the Tacr2 receptor gene in rats. We found that the CUMS-sensitive rats exhibited a decrease in body weight and sucrose preference, a decrease in the distance traveled, rearing frequency and velocity in the open field test, and an increase in immobility time in the FST. Compared with the expression in the control rats, Tacr2 protein and mRNA expression in the hypothalamus significantly increased in the CUMS-sensitive rats; however, the DNA methylation levels of the Tacr2 gene were significantly lower than in the control rats. In summary, according to our findings, the stress-induced increase in Tacr2 expression in the hypothalamus correlated with a specific decrease in DNA methylation of the Tacr2 gene. These results may enrich the understanding of the pathological processes of depression and provide insights into therapeutic approaches for its treatment. |
doi_str_mv | 10.1016/j.bbr.2019.01.059 |
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Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional processes. However, the extent, to which stress impacts Tacr2 expression remains unclear. The molecular mechanisms underlying depression also remain poorly understood. In this study, we subjected adult male Sprague Dawley (SD) rats to chronic unpredictable mild stress (CUMS) to induce a depression-like phenotype. We then measured the body weight and performed the sucrose preference test, forced swimming test (FST) and open field test to detect the effects of stress on anhedonia and activity. Western blotting and real-time PCR were used to study the protein and mRNA expression levels of Tacr2, respectively, in the hypothalamus. To explore DNA methylation of the Tacr2 gene, we used methylated DNA immunoprecipitation sequencing (MeDIP-seq). Additionally, we used the bisulfite sequencing PCR (BSP) to further verify the DNA methylation levels of the Tacr2 receptor gene in rats. We found that the CUMS-sensitive rats exhibited a decrease in body weight and sucrose preference, a decrease in the distance traveled, rearing frequency and velocity in the open field test, and an increase in immobility time in the FST. Compared with the expression in the control rats, Tacr2 protein and mRNA expression in the hypothalamus significantly increased in the CUMS-sensitive rats; however, the DNA methylation levels of the Tacr2 gene were significantly lower than in the control rats. In summary, according to our findings, the stress-induced increase in Tacr2 expression in the hypothalamus correlated with a specific decrease in DNA methylation of the Tacr2 gene. These results may enrich the understanding of the pathological processes of depression and provide insights into therapeutic approaches for its treatment.</description><identifier>ISSN: 0166-4328</identifier><identifier>EISSN: 1872-7549</identifier><identifier>DOI: 10.1016/j.bbr.2019.01.059</identifier><identifier>PMID: 30711443</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Body Weight ; Corticosterone - metabolism ; Corticotropin-Releasing Hormone - metabolism ; CUMS ; Depression ; Depression - genetics ; Depression - metabolism ; Depressive Disorder - genetics ; Depressive Disorder - metabolism ; Disease Models, Animal ; DNA Methylation ; Gene Expression ; Hypothalamo-Hypophyseal System - metabolism ; Hypothalamus - metabolism ; Male ; Pituitary-Adrenal System - metabolism ; Rats ; Rats, Sprague-Dawley ; Receptors, Neurokinin-2 - genetics ; Receptors, Neurokinin-2 - metabolism ; Stress, Psychological - genetics ; Stress, Psychological - metabolism ; Sucrose - metabolism ; Tachykinin ; Tacr2</subject><ispartof>Behavioural brain research, 2019-06, Vol.365, p.103-109</ispartof><rights>2019</rights><rights>Copyright © 2019. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-3cc309274e6f985a659ffd128c26ea5d7239cb83065ecbe03a3f43bee01006513</citedby><cites>FETCH-LOGICAL-c353t-3cc309274e6f985a659ffd128c26ea5d7239cb83065ecbe03a3f43bee01006513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbr.2019.01.059$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30711443$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiang, Dan</creatorcontrib><creatorcontrib>Xiao, Jiawei</creatorcontrib><creatorcontrib>Fu, Linyan</creatorcontrib><creatorcontrib>Yao, Lihua</creatorcontrib><creatorcontrib>Wan, Qirong</creatorcontrib><creatorcontrib>Xiao, Ling</creatorcontrib><creatorcontrib>Zhu, Fan</creatorcontrib><creatorcontrib>Wang, Gaohua</creatorcontrib><creatorcontrib>Liu, Zhongchun</creatorcontrib><title>DNA methylation of the Tacr2 gene in a CUMS model of depression</title><title>Behavioural brain research</title><addtitle>Behav Brain Res</addtitle><description>•We measured the changes of Tacr2 expression in the hypothalamus of CUMS-sensitive rats.•Stress may change the DNA methylation levels of the CpG island in Tacr2 promoter region.•Tacr2 expression of CUMS-sensitive rats may correlated with the DNA methylation of Tacr2 gene..
Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional processes. However, the extent, to which stress impacts Tacr2 expression remains unclear. The molecular mechanisms underlying depression also remain poorly understood. In this study, we subjected adult male Sprague Dawley (SD) rats to chronic unpredictable mild stress (CUMS) to induce a depression-like phenotype. We then measured the body weight and performed the sucrose preference test, forced swimming test (FST) and open field test to detect the effects of stress on anhedonia and activity. Western blotting and real-time PCR were used to study the protein and mRNA expression levels of Tacr2, respectively, in the hypothalamus. To explore DNA methylation of the Tacr2 gene, we used methylated DNA immunoprecipitation sequencing (MeDIP-seq). Additionally, we used the bisulfite sequencing PCR (BSP) to further verify the DNA methylation levels of the Tacr2 receptor gene in rats. We found that the CUMS-sensitive rats exhibited a decrease in body weight and sucrose preference, a decrease in the distance traveled, rearing frequency and velocity in the open field test, and an increase in immobility time in the FST. Compared with the expression in the control rats, Tacr2 protein and mRNA expression in the hypothalamus significantly increased in the CUMS-sensitive rats; however, the DNA methylation levels of the Tacr2 gene were significantly lower than in the control rats. In summary, according to our findings, the stress-induced increase in Tacr2 expression in the hypothalamus correlated with a specific decrease in DNA methylation of the Tacr2 gene. These results may enrich the understanding of the pathological processes of depression and provide insights into therapeutic approaches for its treatment.</description><subject>Animals</subject><subject>Body Weight</subject><subject>Corticosterone - metabolism</subject><subject>Corticotropin-Releasing Hormone - metabolism</subject><subject>CUMS</subject><subject>Depression</subject><subject>Depression - genetics</subject><subject>Depression - metabolism</subject><subject>Depressive Disorder - genetics</subject><subject>Depressive Disorder - metabolism</subject><subject>Disease Models, Animal</subject><subject>DNA Methylation</subject><subject>Gene Expression</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Hypothalamus - metabolism</subject><subject>Male</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Neurokinin-2 - genetics</subject><subject>Receptors, Neurokinin-2 - metabolism</subject><subject>Stress, Psychological - genetics</subject><subject>Stress, Psychological - metabolism</subject><subject>Sucrose - metabolism</subject><subject>Tachykinin</subject><subject>Tacr2</subject><issn>0166-4328</issn><issn>1872-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLAzEUhYMotlZ_gBvJ0s2MN495BBci9QlVF7brkMnc0SnzqMlU6L83pdWlqwuH7xy4HyHnDGIGLL1axkXhYg5MxcBiSNQBGbM841GWSHVIxoFJIyl4PiIn3i8BQELCjslIQMaYlGJMbu5eb2mLw-emMUPdd7Sv6PCJdG6s4_QDO6R1Rw2dLl7eaduX2GyJElcOvQ_8KTmqTOPxbH8nZPFwP58-RbO3x-fp7SyyIhFDJKwVoHgmMa1Unpg0UVVVMp5bnqJJyowLZYtcQJqgLRCEEZUUBSIwCBkTE3K52125_muNftBt7S02jemwX3vNWaZknqWgAsp2qHW99w4rvXJ1a9xGM9Bbb3qpgze99aaB6eAtdC728-uixfKv8SsqANc7AMOT3zU67W2NncWydmgHXfb1P_M_F2Z6_Q</recordid><startdate>20190603</startdate><enddate>20190603</enddate><creator>Xiang, Dan</creator><creator>Xiao, Jiawei</creator><creator>Fu, Linyan</creator><creator>Yao, Lihua</creator><creator>Wan, Qirong</creator><creator>Xiao, Ling</creator><creator>Zhu, Fan</creator><creator>Wang, Gaohua</creator><creator>Liu, Zhongchun</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></search><sort><creationdate>20190603</creationdate><title>DNA methylation of the Tacr2 gene in a CUMS model of depression</title><author>Xiang, Dan ; Xiao, Jiawei ; Fu, Linyan ; Yao, Lihua ; Wan, Qirong ; Xiao, Ling ; Zhu, Fan ; Wang, Gaohua ; Liu, Zhongchun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-3cc309274e6f985a659ffd128c26ea5d7239cb83065ecbe03a3f43bee01006513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Body Weight</topic><topic>Corticosterone - metabolism</topic><topic>Corticotropin-Releasing Hormone - metabolism</topic><topic>CUMS</topic><topic>Depression</topic><topic>Depression - genetics</topic><topic>Depression - metabolism</topic><topic>Depressive Disorder - genetics</topic><topic>Depressive Disorder - metabolism</topic><topic>Disease Models, Animal</topic><topic>DNA Methylation</topic><topic>Gene Expression</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Hypothalamus - metabolism</topic><topic>Male</topic><topic>Pituitary-Adrenal System - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Neurokinin-2 - genetics</topic><topic>Receptors, Neurokinin-2 - metabolism</topic><topic>Stress, Psychological - genetics</topic><topic>Stress, Psychological - metabolism</topic><topic>Sucrose - metabolism</topic><topic>Tachykinin</topic><topic>Tacr2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiang, Dan</creatorcontrib><creatorcontrib>Xiao, Jiawei</creatorcontrib><creatorcontrib>Fu, Linyan</creatorcontrib><creatorcontrib>Yao, Lihua</creatorcontrib><creatorcontrib>Wan, Qirong</creatorcontrib><creatorcontrib>Xiao, Ling</creatorcontrib><creatorcontrib>Zhu, Fan</creatorcontrib><creatorcontrib>Wang, Gaohua</creatorcontrib><creatorcontrib>Liu, Zhongchun</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><jtitle>Behavioural brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiang, Dan</au><au>Xiao, Jiawei</au><au>Fu, Linyan</au><au>Yao, Lihua</au><au>Wan, Qirong</au><au>Xiao, Ling</au><au>Zhu, Fan</au><au>Wang, Gaohua</au><au>Liu, Zhongchun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA methylation of the Tacr2 gene in a CUMS model of depression</atitle><jtitle>Behavioural brain research</jtitle><addtitle>Behav Brain Res</addtitle><date>2019-06-03</date><risdate>2019</risdate><volume>365</volume><spage>103</spage><epage>109</epage><pages>103-109</pages><issn>0166-4328</issn><eissn>1872-7549</eissn><abstract>•We measured the changes of Tacr2 expression in the hypothalamus of CUMS-sensitive rats.•Stress may change the DNA methylation levels of the CpG island in Tacr2 promoter region.•Tacr2 expression of CUMS-sensitive rats may correlated with the DNA methylation of Tacr2 gene..
Tacr2, the gene encoding the NK2 receptor, belongs to G protein-coupled receptors. Accumulating evidence has indicated that the tachykinin receptors may contribute to the pathophysiology of depression. During the last decade, some studies have shown that Tacr2 activation is involved in the modulation of emotional processes. However, the extent, to which stress impacts Tacr2 expression remains unclear. The molecular mechanisms underlying depression also remain poorly understood. In this study, we subjected adult male Sprague Dawley (SD) rats to chronic unpredictable mild stress (CUMS) to induce a depression-like phenotype. We then measured the body weight and performed the sucrose preference test, forced swimming test (FST) and open field test to detect the effects of stress on anhedonia and activity. Western blotting and real-time PCR were used to study the protein and mRNA expression levels of Tacr2, respectively, in the hypothalamus. To explore DNA methylation of the Tacr2 gene, we used methylated DNA immunoprecipitation sequencing (MeDIP-seq). Additionally, we used the bisulfite sequencing PCR (BSP) to further verify the DNA methylation levels of the Tacr2 receptor gene in rats. We found that the CUMS-sensitive rats exhibited a decrease in body weight and sucrose preference, a decrease in the distance traveled, rearing frequency and velocity in the open field test, and an increase in immobility time in the FST. Compared with the expression in the control rats, Tacr2 protein and mRNA expression in the hypothalamus significantly increased in the CUMS-sensitive rats; however, the DNA methylation levels of the Tacr2 gene were significantly lower than in the control rats. In summary, according to our findings, the stress-induced increase in Tacr2 expression in the hypothalamus correlated with a specific decrease in DNA methylation of the Tacr2 gene. These results may enrich the understanding of the pathological processes of depression and provide insights into therapeutic approaches for its treatment.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30711443</pmid><doi>10.1016/j.bbr.2019.01.059</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Body Weight Corticosterone - metabolism Corticotropin-Releasing Hormone - metabolism CUMS Depression Depression - genetics Depression - metabolism Depressive Disorder - genetics Depressive Disorder - metabolism Disease Models, Animal DNA Methylation Gene Expression Hypothalamo-Hypophyseal System - metabolism Hypothalamus - metabolism Male Pituitary-Adrenal System - metabolism Rats Rats, Sprague-Dawley Receptors, Neurokinin-2 - genetics Receptors, Neurokinin-2 - metabolism Stress, Psychological - genetics Stress, Psychological - metabolism Sucrose - metabolism Tachykinin Tacr2 |
title | DNA methylation of the Tacr2 gene in a CUMS model of depression |
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