<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-02T14:42:51Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/45018" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/45018</identifier><datestamp>2026-01-30T00:46:56Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>FGFR1-5-HT1A Heteroreceptor Complexes: Implications for Understanding and Treating Major Depression</dc:title>
   <dc:creator>Borroto-Escuela, Dasiel O.</dc:creator>
   <dc:creator>Tarakanov, Alexander O.</dc:creator>
   <dc:creator>Fuxe, Kjell</dc:creator>
   <dc:subject>Receptores de neurotransmisores</dc:subject>
   <dc:subject>Depresión</dc:subject>
   <dcterms:abstract>The serotonin and neurotrophic factor hypotheses of depression are well known. The discovery of brain fibroblast growth factor receptor 1 (FGFR1)-5 hydroxytryptamine receptor 1A (5-HT1A) heteroreceptor complexes, and their enhancement of neuroplasticity, offers an integration of these hypotheses at the molecular level. They were first described in the hippocampus and later in midbrain 5-HT neurons, where these heterocomplexes are enriched in 5-HT1A autoreceptors. Combined FGF2 and 5-HT1A agonist treatment increased the formation of these heterocomplexes and the facilitatory allosteric receptor-receptor interactions within them led to the enhancement of FGFR1 signaling and was associated with the development of antidepressant effects. We discuss these findings with regard to a theory of motifs critically involved in these interactions and suggest that these complexes represent novel targets for antidepressants. 5-HT1A receptor is a 5-HT receptor subtype, which binds the endogenous transmitter 5-hydroxytryptamine. In the brain it participates in mediating antidepressant effects of classical antidepressant drugs and of serotonin selective reuptake inhibitors.FGFR1 is a receptor tyrosine kinase, the ligands of which are specific members of the fibroblast growth factor family. One of its ligands, FGF2, is shown to produce antidepressant-like effects.FGFR1-5-HT1A heteroreceptor complexes were recently discovered in the brain. In these heterocomplexes, agonist coactivation markedly enhanced FGFR1 signaling leading to increased neuroplasticity and antidepressant-like actions.The FGFR1-5-HT1A heteroreceptor complex represents a new promising target for antidepressant drugs including combined treatment with FGF2 and 5-HT1A agonists in major depression.</dcterms:abstract>
   <dcterms:issued>2016-01-01</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>FGFR1–5-HT1A Heteroreceptor Complexes: Implications for Understanding and Treating Major Depression Borroto-Escuela, Dasiel O. et al. Trends in Neurosciences, Volume 39, Issue 1, 5 - 15</dc:identifier>
   <dc:identifier>01662236</dc:identifier>
   <dc:identifier>https://doi.org/10.5281/zenodo.13860084</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/45018</dc:identifier>
   <dc:identifier>10.1016/j.tins.2015.11.003</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/grantAgreement/Swedish_Research_Council//62X-00715-50-3/SE///</dc:relation>
   <dc:relation>info:eu-repo/grantAgreement/AFA_Forsakring//130328/SE///</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
</qdc:qualifieddc>
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