Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression
In depression, disrupted circadian rhythms reflect abnormalities in the central circadian pacemaker, the hypothalamic suprachiasmatic nucleus (SCN). Although many SCN neurons are said to be GABAergic, it was not yet known whether and how SCN GABA changes occur in the SCN in depression. We, therefore...
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Veröffentlicht in: | Brain Structure and Function 2017-12, Vol.222 (9), p.4079-4088 |
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description | In depression, disrupted circadian rhythms reflect abnormalities in the central circadian pacemaker, the hypothalamic suprachiasmatic nucleus (SCN). Although many SCN neurons are said to be GABAergic, it was not yet known whether and how SCN GABA changes occur in the SCN in depression. We, therefore, studied GABA in the SCN in relation to the changes in arginine vasopressin (AVP), which is one of the major SCN output systems. Postmortem hypothalamus specimens of 13 subjects suffering from depression and of 13 well-matched controls were collected. Quantitative immunocytochemistry was used to analyze the protein levels of glutamic acid decarboxylase (GAD)65/67 and AVP, and quantitative in situ hybridization was used to measure transcript levels of GAD67 in the SCN. There were a significant 58% increase of SCN GAD65/67-ir and a significant 169% increase of SCN GAD67-mRNA in the depression group. In addition, there were a significant 253% increase of AVP-ir in female depression subjects but not in male depression patients. This sex difference was supported by a re-analysis of SCN AVP-ir data of a previous study of our group. Moreover, SCN-AVP-ir showed a significant negative correlation with age in the control group and in the male, but not in the female depression group. Given the crucial role of GABA in mediating SCN function, our finding of increased SCN GABA expression may significantly contribute to the disordered circadian rhythms in depression. The increased SCN AVP-ir in female—but not in male-depression patients—may reflect the higher vulnerability for depression in women. |
doi_str_mv | 10.1007/s00429-017-1442-y |
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Although many SCN neurons are said to be GABAergic, it was not yet known whether and how SCN GABA changes occur in the SCN in depression. We, therefore, studied GABA in the SCN in relation to the changes in arginine vasopressin (AVP), which is one of the major SCN output systems. Postmortem hypothalamus specimens of 13 subjects suffering from depression and of 13 well-matched controls were collected. Quantitative immunocytochemistry was used to analyze the protein levels of glutamic acid decarboxylase (GAD)65/67 and AVP, and quantitative in situ hybridization was used to measure transcript levels of GAD67 in the SCN. There were a significant 58% increase of SCN GAD65/67-ir and a significant 169% increase of SCN GAD67-mRNA in the depression group. In addition, there were a significant 253% increase of AVP-ir in female depression subjects but not in male depression patients. This sex difference was supported by a re-analysis of SCN AVP-ir data of a previous study of our group. Moreover, SCN-AVP-ir showed a significant negative correlation with age in the control group and in the male, but not in the female depression group. Given the crucial role of GABA in mediating SCN function, our finding of increased SCN GABA expression may significantly contribute to the disordered circadian rhythms in depression. The increased SCN AVP-ir in female—but not in male-depression patients—may reflect the higher vulnerability for depression in women.</description><identifier>ISSN: 1863-2653</identifier><identifier>EISSN: 1863-2661</identifier><identifier>EISSN: 0340-2061</identifier><identifier>DOI: 10.1007/s00429-017-1442-y</identifier><identifier>PMID: 28608287</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Argipressin ; Biological clocks ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Circadian rhythm ; Circadian rhythms ; Glutamic acid ; Hypothalamus ; Immunocytochemistry ; Mental depression ; Neurology ; Neurosciences ; Original ; Original Article ; Suprachiasmatic nucleus ; Transcription ; Vasopressin ; γ-Aminobutyric acid</subject><ispartof>Brain Structure and Function, 2017-12, Vol.222 (9), p.4079-4088</ispartof><rights>The Author(s) 2017</rights><rights>Brain Structure and Function is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-dd07f382eebf3abfdd12e25cb75b830201802eb867b3a3d196f2151e8cd9a0d73</citedby><cites>FETCH-LOGICAL-c470t-dd07f382eebf3abfdd12e25cb75b830201802eb867b3a3d196f2151e8cd9a0d73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00429-017-1442-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00429-017-1442-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28608287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Xueyan</creatorcontrib><creatorcontrib>Balesar, Rawien</creatorcontrib><creatorcontrib>Lu, Jing</creatorcontrib><creatorcontrib>Farajnia, Sahar</creatorcontrib><creatorcontrib>Zhu, Qiongbin</creatorcontrib><creatorcontrib>Huang, Manli</creatorcontrib><creatorcontrib>Bao, Ai-Min</creatorcontrib><creatorcontrib>Swaab, Dick F.</creatorcontrib><title>Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression</title><title>Brain Structure and Function</title><addtitle>Brain Struct Funct</addtitle><addtitle>Brain Struct Funct</addtitle><description>In depression, disrupted circadian rhythms reflect abnormalities in the central circadian pacemaker, the hypothalamic suprachiasmatic nucleus (SCN). Although many SCN neurons are said to be GABAergic, it was not yet known whether and how SCN GABA changes occur in the SCN in depression. We, therefore, studied GABA in the SCN in relation to the changes in arginine vasopressin (AVP), which is one of the major SCN output systems. Postmortem hypothalamus specimens of 13 subjects suffering from depression and of 13 well-matched controls were collected. Quantitative immunocytochemistry was used to analyze the protein levels of glutamic acid decarboxylase (GAD)65/67 and AVP, and quantitative in situ hybridization was used to measure transcript levels of GAD67 in the SCN. There were a significant 58% increase of SCN GAD65/67-ir and a significant 169% increase of SCN GAD67-mRNA in the depression group. In addition, there were a significant 253% increase of AVP-ir in female depression subjects but not in male depression patients. This sex difference was supported by a re-analysis of SCN AVP-ir data of a previous study of our group. Moreover, SCN-AVP-ir showed a significant negative correlation with age in the control group and in the male, but not in the female depression group. Given the crucial role of GABA in mediating SCN function, our finding of increased SCN GABA expression may significantly contribute to the disordered circadian rhythms in depression. The increased SCN AVP-ir in female—but not in male-depression patients—may reflect the higher vulnerability for depression in women.</description><subject>Argipressin</subject><subject>Biological clocks</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Circadian rhythm</subject><subject>Circadian rhythms</subject><subject>Glutamic acid</subject><subject>Hypothalamus</subject><subject>Immunocytochemistry</subject><subject>Mental depression</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Original</subject><subject>Original Article</subject><subject>Suprachiasmatic nucleus</subject><subject>Transcription</subject><subject>Vasopressin</subject><subject>γ-Aminobutyric acid</subject><issn>1863-2653</issn><issn>1863-2661</issn><issn>0340-2061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kc1O3DAUha2qVaG0D9ANitQNm7T-SWxng4QQFCSkbtq15dg3E48SO9gJIm-PpwMjitSVbZ3vHPv6IPSV4O8EY_EjYVzRpsRElKSqaLm-Q8dEclZSzsn7w75mR-hTSluM60aS5iM6opJjSaU4RttbbyLoBLbYDMusR2cKbZwtLBgd2_C4Dlks4HGKkJILvnC-mHso-nUKc6-Hv460TFGb3uk06jmf_WIGWNKOtfDi_Iw-dHpI8OV5PUF_rq9-X96Ud79-3l5e3JWmEngurcWiY5ICtB3TbWctoUBr04q6lQxTTCSm0EouWqaZJQ3vKKkJSGMbja1gJ-h8nzst7QjWgJ-jHtQU3ajjqoJ26l_Fu15twoOqueT553LA2XNADPcLpFmNLhkYBu0hLEmRBjeUiqpqMvrtDboNS_R5vExxJivKOMsU2VMmhpQidIfHEKx2Tap9kyo3qXZNqjV7Tl9PcXC8VJcBugdSlvwG4qur_5v6BDEorWU</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Wu, Xueyan</creator><creator>Balesar, Rawien</creator><creator>Lu, Jing</creator><creator>Farajnia, Sahar</creator><creator>Zhu, Qiongbin</creator><creator>Huang, Manli</creator><creator>Bao, Ai-Min</creator><creator>Swaab, Dick F.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171201</creationdate><title>Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression</title><author>Wu, Xueyan ; Balesar, Rawien ; Lu, Jing ; Farajnia, Sahar ; Zhu, Qiongbin ; Huang, Manli ; Bao, Ai-Min ; Swaab, Dick F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-dd07f382eebf3abfdd12e25cb75b830201802eb867b3a3d196f2151e8cd9a0d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Argipressin</topic><topic>Biological clocks</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Circadian rhythm</topic><topic>Circadian rhythms</topic><topic>Glutamic acid</topic><topic>Hypothalamus</topic><topic>Immunocytochemistry</topic><topic>Mental depression</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Original</topic><topic>Original Article</topic><topic>Suprachiasmatic nucleus</topic><topic>Transcription</topic><topic>Vasopressin</topic><topic>γ-Aminobutyric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Xueyan</creatorcontrib><creatorcontrib>Balesar, Rawien</creatorcontrib><creatorcontrib>Lu, Jing</creatorcontrib><creatorcontrib>Farajnia, Sahar</creatorcontrib><creatorcontrib>Zhu, Qiongbin</creatorcontrib><creatorcontrib>Huang, Manli</creatorcontrib><creatorcontrib>Bao, Ai-Min</creatorcontrib><creatorcontrib>Swaab, Dick F.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech 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>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain Structure and Function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Xueyan</au><au>Balesar, Rawien</au><au>Lu, Jing</au><au>Farajnia, Sahar</au><au>Zhu, Qiongbin</au><au>Huang, Manli</au><au>Bao, Ai-Min</au><au>Swaab, Dick F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression</atitle><jtitle>Brain Structure and Function</jtitle><stitle>Brain Struct Funct</stitle><addtitle>Brain Struct Funct</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>222</volume><issue>9</issue><spage>4079</spage><epage>4088</epage><pages>4079-4088</pages><issn>1863-2653</issn><eissn>1863-2661</eissn><eissn>0340-2061</eissn><abstract>In depression, disrupted circadian rhythms reflect abnormalities in the central circadian pacemaker, the hypothalamic suprachiasmatic nucleus (SCN). Although many SCN neurons are said to be GABAergic, it was not yet known whether and how SCN GABA changes occur in the SCN in depression. We, therefore, studied GABA in the SCN in relation to the changes in arginine vasopressin (AVP), which is one of the major SCN output systems. Postmortem hypothalamus specimens of 13 subjects suffering from depression and of 13 well-matched controls were collected. Quantitative immunocytochemistry was used to analyze the protein levels of glutamic acid decarboxylase (GAD)65/67 and AVP, and quantitative in situ hybridization was used to measure transcript levels of GAD67 in the SCN. There were a significant 58% increase of SCN GAD65/67-ir and a significant 169% increase of SCN GAD67-mRNA in the depression group. In addition, there were a significant 253% increase of AVP-ir in female depression subjects but not in male depression patients. This sex difference was supported by a re-analysis of SCN AVP-ir data of a previous study of our group. Moreover, SCN-AVP-ir showed a significant negative correlation with age in the control group and in the male, but not in the female depression group. Given the crucial role of GABA in mediating SCN function, our finding of increased SCN GABA expression may significantly contribute to the disordered circadian rhythms in depression. The increased SCN AVP-ir in female—but not in male-depression patients—may reflect the higher vulnerability for depression in women.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28608287</pmid><doi>10.1007/s00429-017-1442-y</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Argipressin Biological clocks Biomedical and Life Sciences Biomedicine Cell Biology Circadian rhythm Circadian rhythms Glutamic acid Hypothalamus Immunocytochemistry Mental depression Neurology Neurosciences Original Original Article Suprachiasmatic nucleus Transcription Vasopressin γ-Aminobutyric acid |
title | Increased glutamic acid decarboxylase expression in the hypothalamic suprachiasmatic nucleus in depression |
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