<?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>2026-05-31T22:28:56Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/31876" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/31876</identifier><datestamp>2026-02-03T12:32:52Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</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">Infantes-López, María Inmaculada</subfield>
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      <subfield code="a">Zambrana-Infantes, Emma</subfield>
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      <subfield code="a">Chaves-Peña, Patricia</subfield>
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      <subfield code="a">Nieto-Quero, Andrea</subfield>
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      <subfield code="a">Muñoz-Martín, José</subfield>
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      <subfield code="a">Zea-Doña, Alejandro</subfield>
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      <subfield code="a">Pedraza-Benítez, María del Carmen</subfield>
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      <subfield code="a">Pérez-Martín, Margarita</subfield>
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      <subfield code="a">Depression is a concerning public health threat highly associated with stress. Stress increases brain immune alterations, namely in&#xd;
microglia, which can affect neuron physiology, like neurogenesis, causing a depressive-like behavior. However, despite depression being twice as frequent&#xd;
in females, most studies have been done in males. This results in a gap in our current understanding of stress processing in both sexes, and consequently&#xd;
in our current therapeutical approach.&#xd;
Here, we used the social defeat stress (SDS) paradigm in 8-week-old male and female C57BL/6J mice for 10 consecutive days. Anhedonic and social&#xd;
behavior were assessed to evaluate depressive-like traits. Using immunohistochemical and computer image analysis, microglial distribution, morphology,&#xd;
and neuronal maturation were analyzed in the dentate gyrus of the hippocampus.&#xd;
Results show a different response to SDS in both sexes. Microglial morphological activation was enhanced in the subgranular cell layer of the male dentate&#xd;
gyrus, yet it was not affected in females. In turn, both sexes showed lower neurogenesis, especially in the supra cell layer. Strikingly, female mice&#xd;
neurogenesis was affected in earlier stages of maturation, whereas males showed greater alteration in later maturation steps. In male mice, this&#xd;
impairment was statistically mediated by the microglia, unlike in females where microglia seemed unrelated. Also, males showed a deeper social disability,&#xd;
whereas females had a greater anhedonic profile.&#xd;
As a conclusion, female and male mice responding differently to stress proved that our current approach to depression might need to change to adapt to&#xd;
differential alterations in both sexes.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/31876</subfield>
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      <subfield code="a">Neurobiología del desarrollo</subfield>
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      <subfield code="a">Depresión mental - Diferencias sexuales</subfield>
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      <subfield code="a">Modelos animales en investigación</subfield>
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      <subfield code="a">Female microglia and neurogenesis respond differently to social defeat stress compared to males.</subfield>
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