The Association Between Antidepressant Effect of SSRIs and Astrocytes: Conceptual Overview and Meta‐analysis of the Literature
Major depressive disorders (MDD) a worldwide psychiatric disease, is yet to be adequately controlled by therapies; while the mechanisms of action of antidepressants are yet to be fully characterised. In the last two decades, an increasing number of studies have demonstrated the role of astrocytes in...
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description | Major depressive disorders (MDD) a worldwide psychiatric disease, is yet to be adequately controlled by therapies; while the mechanisms of action of antidepressants are yet to be fully characterised. In the last two decades, an increasing number of studies have demonstrated the role of astrocytes in the pathophysiology and therapy of MDD. Selective serotonin reuptake inhibitors (SSRIs) are the most widely used antidepressants. It is generally acknowledged that SSRIs increase serotonin levels in the central nervous system by inhibiting serotonin transporters, although the SSRIs action is not ideal. The SSRIs antidepressant effect develops with considerable delay; their efficacy is low and frequent relapses are common. Neither cellular nor molecular pharmacological mechanisms of SSRIs are fully characterised; in particular their action on astrocytes remain underappreciated. In this paper we overview potential therapeutic mechanisms of SSRIs associated with astroglia and report the results of meta-analysis of studies dedicated to MDD, SSRIs and astrocytes. In particular, we argue that fluoxetine, the representative SSRI, improves depressive-like behaviours in animals treated with chronic mild stress and reverses depression-associated decrease in astrocytic glial fibrillary acidic protein (GFAP) expression. In addition, fluoxetine upregulates astrocytic mRNA expression of 5-hydroxytriptamin/serotonin
2B
receptors (5-HT
2B
R). In summary, we infer that SSRIs exert their anti-depressant effect by regulating several molecular and signalling pathways in astrocytes. |
doi_str_mv | 10.1007/s11064-020-03225-6 |
format | Article |
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2B
receptors (5-HT
2B
R). In summary, we infer that SSRIs exert their anti-depressant effect by regulating several molecular and signalling pathways in astrocytes.</description><identifier>ISSN: 0364-3190</identifier><identifier>ISSN: 1573-6903</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1007/s11064-020-03225-6</identifier><identifier>PMID: 33527219</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animal behavior ; Animals ; Antidepressants ; Antidepressive Agents - therapeutic use ; Astrocytes ; Astrocytes - drug effects ; Astrocytes - metabolism ; Behavior, Animal - drug effects ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Cell Count ; Central nervous system ; Depressive Disorder, Major - drug therapy ; Depressive Disorder, Major - metabolism ; Fluoxetine ; Gene expression ; Glial fibrillary acidic protein ; Glial Fibrillary Acidic Protein - metabolism ; Humans ; Mental depression ; Mental disorders ; Meta-analysis ; Mice ; Neurochemistry ; Neurology ; Neurosciences ; Original Paper ; Pathophysiology ; Rats ; Receptors, Serotonin, 5-HT2 - metabolism ; Reviews ; Selective Serotonin Reuptake Inhibitors - therapeutic use ; Serotonin ; Serotonin S2 receptors ; Serotonin uptake inhibitors ; Signal transduction</subject><ispartof>Neurochemical research, 2021-10, Vol.46 (10), p.2731-2745</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-91acf3344d79e6f059cfff0ad695ddeb05266c9418bf8c76608f7a62afc4b7cf3</citedby><cites>FETCH-LOGICAL-c375t-91acf3344d79e6f059cfff0ad695ddeb05266c9418bf8c76608f7a62afc4b7cf3</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/s11064-020-03225-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11064-020-03225-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33527219$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Beina</creatorcontrib><creatorcontrib>Zhang, Manman</creatorcontrib><creatorcontrib>Ji, Ming</creatorcontrib><creatorcontrib>Gong, Wenliang</creatorcontrib><creatorcontrib>Chen, Binjie</creatorcontrib><creatorcontrib>Zorec, Robert</creatorcontrib><creatorcontrib>Stenovec, Matjaž</creatorcontrib><creatorcontrib>Verkhratsky, Alexei</creatorcontrib><creatorcontrib>Li, Baoman</creatorcontrib><title>The Association Between Antidepressant Effect of SSRIs and Astrocytes: Conceptual Overview and Meta‐analysis of the Literature</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><addtitle>Neurochem Res</addtitle><description>Major depressive disorders (MDD) a worldwide psychiatric disease, is yet to be adequately controlled by therapies; while the mechanisms of action of antidepressants are yet to be fully characterised. In the last two decades, an increasing number of studies have demonstrated the role of astrocytes in the pathophysiology and therapy of MDD. Selective serotonin reuptake inhibitors (SSRIs) are the most widely used antidepressants. It is generally acknowledged that SSRIs increase serotonin levels in the central nervous system by inhibiting serotonin transporters, although the SSRIs action is not ideal. The SSRIs antidepressant effect develops with considerable delay; their efficacy is low and frequent relapses are common. Neither cellular nor molecular pharmacological mechanisms of SSRIs are fully characterised; in particular their action on astrocytes remain underappreciated. In this paper we overview potential therapeutic mechanisms of SSRIs associated with astroglia and report the results of meta-analysis of studies dedicated to MDD, SSRIs and astrocytes. In particular, we argue that fluoxetine, the representative SSRI, improves depressive-like behaviours in animals treated with chronic mild stress and reverses depression-associated decrease in astrocytic glial fibrillary acidic protein (GFAP) expression. In addition, fluoxetine upregulates astrocytic mRNA expression of 5-hydroxytriptamin/serotonin
2B
receptors (5-HT
2B
R). In summary, we infer that SSRIs exert their anti-depressant effect by regulating several molecular and signalling pathways in astrocytes.</description><subject>Animal behavior</subject><subject>Animals</subject><subject>Antidepressants</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Astrocytes</subject><subject>Astrocytes - drug effects</subject><subject>Astrocytes - metabolism</subject><subject>Behavior, Animal - drug effects</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Cell Count</subject><subject>Central nervous system</subject><subject>Depressive Disorder, Major - drug therapy</subject><subject>Depressive Disorder, Major - metabolism</subject><subject>Fluoxetine</subject><subject>Gene expression</subject><subject>Glial fibrillary acidic protein</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Humans</subject><subject>Mental depression</subject><subject>Mental disorders</subject><subject>Meta-analysis</subject><subject>Mice</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Original Paper</subject><subject>Pathophysiology</subject><subject>Rats</subject><subject>Receptors, Serotonin, 5-HT2 - metabolism</subject><subject>Reviews</subject><subject>Selective Serotonin Reuptake Inhibitors - therapeutic use</subject><subject>Serotonin</subject><subject>Serotonin S2 receptors</subject><subject>Serotonin uptake inhibitors</subject><subject>Signal transduction</subject><issn>0364-3190</issn><issn>1573-6903</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><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>eNp9kc9uEzEQhy0EoqHwAhyQJS5ctvjP2o65hajQSkGVaDlbjncMW23WweNtlVsfgWfkSXCbAlIPPc1hvu83Gv0Iec3ZEWfMvEfOmW4bJljDpBCq0U_IjCsjG22ZfEpmTNa15JYdkBeIl4xVTfDn5EBKJYzgdkZuLn4AXSCm0PvSp5F-hHINMNLFWPoOthkQ_VjocYwQCk2Rnp9_PUXqx65qJaewK4Af6DKNAbZl8gM9u4J81cP1HfMFiv9988uPfthhj7cBpV5c9QWyL1OGl-RZ9APCq_t5SL59Or5YnjSrs8-ny8WqCdKo0ljuQ5SybTtjQUembIgxMt9pq7oO1kwJrYNt-Xwd58FozebReC18DO3aVPWQvNvnbnP6OQEWt-kxwDD4EdKETrRzpQQz3FT07QP0Mk25flApZSpjjOWVEnsq5ISYIbpt7jc-7xxn7rYft-_H1X7cXT9OV-nNffS03kD3T_lbSAXkHsC6Gr9D_n_7kdg_1sydMw</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Chen, Beina</creator><creator>Zhang, Manman</creator><creator>Ji, Ming</creator><creator>Gong, Wenliang</creator><creator>Chen, Binjie</creator><creator>Zorec, Robert</creator><creator>Stenovec, Matjaž</creator><creator>Verkhratsky, Alexei</creator><creator>Li, Baoman</creator><general>Springer US</general><general>Springer Nature 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>3V.</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</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>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20211001</creationdate><title>The Association Between Antidepressant Effect of SSRIs and Astrocytes: Conceptual Overview and Meta‐analysis of the Literature</title><author>Chen, Beina ; Zhang, Manman ; Ji, Ming ; Gong, Wenliang ; Chen, Binjie ; Zorec, Robert ; Stenovec, Matjaž ; Verkhratsky, Alexei ; Li, Baoman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-91acf3344d79e6f059cfff0ad695ddeb05266c9418bf8c76608f7a62afc4b7cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal behavior</topic><topic>Animals</topic><topic>Antidepressants</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Astrocytes</topic><topic>Astrocytes - drug effects</topic><topic>Astrocytes - metabolism</topic><topic>Behavior, Animal - drug effects</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Cell Count</topic><topic>Central nervous system</topic><topic>Depressive Disorder, Major - drug therapy</topic><topic>Depressive Disorder, Major - metabolism</topic><topic>Fluoxetine</topic><topic>Gene expression</topic><topic>Glial fibrillary acidic protein</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Humans</topic><topic>Mental depression</topic><topic>Mental disorders</topic><topic>Meta-analysis</topic><topic>Mice</topic><topic>Neurochemistry</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Original Paper</topic><topic>Pathophysiology</topic><topic>Rats</topic><topic>Receptors, Serotonin, 5-HT2 - metabolism</topic><topic>Reviews</topic><topic>Selective Serotonin Reuptake Inhibitors - therapeutic use</topic><topic>Serotonin</topic><topic>Serotonin S2 receptors</topic><topic>Serotonin uptake inhibitors</topic><topic>Signal transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Beina</creatorcontrib><creatorcontrib>Zhang, Manman</creatorcontrib><creatorcontrib>Ji, Ming</creatorcontrib><creatorcontrib>Gong, Wenliang</creatorcontrib><creatorcontrib>Chen, Binjie</creatorcontrib><creatorcontrib>Zorec, Robert</creatorcontrib><creatorcontrib>Stenovec, Matjaž</creatorcontrib><creatorcontrib>Verkhratsky, Alexei</creatorcontrib><creatorcontrib>Li, Baoman</creatorcontrib><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>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology 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>ProQuest Pharma Collection</collection><collection>Technology Research Database</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>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</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>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>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>MEDLINE - Academic</collection><jtitle>Neurochemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Beina</au><au>Zhang, Manman</au><au>Ji, Ming</au><au>Gong, Wenliang</au><au>Chen, Binjie</au><au>Zorec, Robert</au><au>Stenovec, Matjaž</au><au>Verkhratsky, Alexei</au><au>Li, Baoman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Association Between Antidepressant Effect of SSRIs and Astrocytes: Conceptual Overview and Meta‐analysis of the Literature</atitle><jtitle>Neurochemical research</jtitle><stitle>Neurochem Res</stitle><addtitle>Neurochem Res</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>46</volume><issue>10</issue><spage>2731</spage><epage>2745</epage><pages>2731-2745</pages><issn>0364-3190</issn><issn>1573-6903</issn><eissn>1573-6903</eissn><abstract>Major depressive disorders (MDD) a worldwide psychiatric disease, is yet to be adequately controlled by therapies; while the mechanisms of action of antidepressants are yet to be fully characterised. In the last two decades, an increasing number of studies have demonstrated the role of astrocytes in the pathophysiology and therapy of MDD. Selective serotonin reuptake inhibitors (SSRIs) are the most widely used antidepressants. It is generally acknowledged that SSRIs increase serotonin levels in the central nervous system by inhibiting serotonin transporters, although the SSRIs action is not ideal. The SSRIs antidepressant effect develops with considerable delay; their efficacy is low and frequent relapses are common. Neither cellular nor molecular pharmacological mechanisms of SSRIs are fully characterised; in particular their action on astrocytes remain underappreciated. In this paper we overview potential therapeutic mechanisms of SSRIs associated with astroglia and report the results of meta-analysis of studies dedicated to MDD, SSRIs and astrocytes. In particular, we argue that fluoxetine, the representative SSRI, improves depressive-like behaviours in animals treated with chronic mild stress and reverses depression-associated decrease in astrocytic glial fibrillary acidic protein (GFAP) expression. In addition, fluoxetine upregulates astrocytic mRNA expression of 5-hydroxytriptamin/serotonin
2B
receptors (5-HT
2B
R). In summary, we infer that SSRIs exert their anti-depressant effect by regulating several molecular and signalling pathways in astrocytes.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>33527219</pmid><doi>10.1007/s11064-020-03225-6</doi><tpages>15</tpages></addata></record> |
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subjects | Animal behavior Animals Antidepressants Antidepressive Agents - therapeutic use Astrocytes Astrocytes - drug effects Astrocytes - metabolism Behavior, Animal - drug effects Biochemistry Biomedical and Life Sciences Biomedicine Cell Biology Cell Count Central nervous system Depressive Disorder, Major - drug therapy Depressive Disorder, Major - metabolism Fluoxetine Gene expression Glial fibrillary acidic protein Glial Fibrillary Acidic Protein - metabolism Humans Mental depression Mental disorders Meta-analysis Mice Neurochemistry Neurology Neurosciences Original Paper Pathophysiology Rats Receptors, Serotonin, 5-HT2 - metabolism Reviews Selective Serotonin Reuptake Inhibitors - therapeutic use Serotonin Serotonin S2 receptors Serotonin uptake inhibitors Signal transduction |
title | The Association Between Antidepressant Effect of SSRIs and Astrocytes: Conceptual Overview and Meta‐analysis of the Literature |
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