<?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>2026-05-31T13:42:31Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/45018" metadataPrefix="marc">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><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Borroto-Escuela, Dasiel O.</subfield>
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      <subfield code="a">Tarakanov, Alexander O.</subfield>
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      <subfield code="a">Fuxe, Kjell</subfield>
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      <subfield code="c">2016-01-01</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">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</subfield>
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      <subfield code="a">01662236</subfield>
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      <subfield code="a">https://doi.org/10.5281/zenodo.13860084</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/45018</subfield>
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      <subfield code="a">10.1016/j.tins.2015.11.003</subfield>
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      <subfield code="a">Receptores de neurotransmisores</subfield>
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      <subfield code="a">Depresión</subfield>
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      <subfield code="a">FGFR1-5-HT1A Heteroreceptor Complexes: Implications for Understanding and Treating Major Depression</subfield>
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