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   <dc:title>Social defeat stress induces microglial alterations and impaired cell  survival in the hypothalamus according to behavioral phenotype</dc:title>
   <dc:creator>Infantes-López, M. Inmaculada</dc:creator>
   <dc:creator>Zambrana-Infantes, Emma</dc:creator>
   <dc:creator>Chaves-Peña, Patricia</dc:creator>
   <dc:creator>Nieto-Quero, Andrea</dc:creator>
   <dc:creator>Muñoz-Martín, José</dc:creator>
   <dc:creator>Pedraza-Benítez, María del Carmen</dc:creator>
   <dc:creator>Pérez-Martín, Margarita</dc:creator>
   <dc:subject>Estrés (Fisiología) - Congresos</dc:subject>
   <dc:subject>Depresión mental -  Efectos del estrés - Congresos</dc:subject>
   <dc:subject>Experimentación animal - Congresos</dc:subject>
   <dc:subject>Microglia - Efectos del estrés - Congresos</dc:subject>
   <dc:subject>Microglia</dc:subject>
   <dc:subject>Hypothalamus</dc:subject>
   <dc:subject>Mice</dc:subject>
   <dc:subject>Cell survival</dc:subject>
   <dc:description>Stress is the main environmental cause for depression, known to cause brain immune &#xd;
alterations. As major brain immune cells, microglia undergo transcriptional and, &#xd;
consequently, morphological changes that result in tissue damage, including new cell &#xd;
generation impairment. Even so, few brain regions have been thoroughly studied, &#xd;
excluding key regulators as the hypothalamus, in which this process remains partially &#xd;
unknown. Moreover, there is a poor understanding in physiology related to behavioral &#xd;
outcome. Therefore, it would be interesting to study the relationship between microglia &#xd;
and cell proliferation in stressed mice while controlling for behavior.&#xd;
Here, we used the social defeat stress (SDS) paradigm as a depression-inducing protocol &#xd;
in 8-week-old male C57BL/6J mice for 10 consecutive days. Intruder mice behavior was &#xd;
analyzed to assess depression using behavioral tests and K-means clustering. By&#xd;
immunohistochemical and imaging procedures, microglial morphology, and &#xd;
distribution, as well as cell survival, were analyzed in the hypothalamic paraventricular, &#xd;
ventromedial and arcuate nucleus. Finally, statistical mediation analysis was conducted&#xd;
to evaluate the relationship among variables. &#xd;
Results show mice response to SDS was different, being half the mice resilient and half&#xd;
sensitive to depressive-like symptoms. Microglial morphological activation was &#xd;
enhanced in the ventromedial and arcuate nucleus, especially in stress sensitive animals. &#xd;
Similar results were observed in cell survival, which was particularly affected in &#xd;
sensitive mice. Strikingly, these cell survival changes were statistically mediated by &#xd;
microglial activation.&#xd;
As a conclusion, hypothalamic regions were found to respond differently to stress,&#xd;
accordingly to behavioral outcome, in terms of microglial activation and subsequent &#xd;
decrease in cell survival.</dc:description>
   <dc:description>This study was supported by FEDER/Ministerio de Ciencia, Innovación y Universidades &#xd;
– Agencia Estatal de Investigación from Spain (PSI2017-83408-P to Pedraza C.),&#xd;
FEDER/Junta de Andalucía from Spain (UMA20-FEDERJA-112 to Pedraza C. and Pérez-&#xd;
Martín M), and Ministerio de Educación, Cultura y Deporte from Spain (FPU19/03629 to &#xd;
Infantes-López MI and FPU16/05308 to Nieto-Quero A).&#xd;
Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.</dc:description>
   <dc:date>2022-07-26T10:32:34Z</dc:date>
   <dc:date>2022-07-26T10:32:34Z</dc:date>
   <dc:date>2022-07</dc:date>
   <dc:type>conference output</dc:type>
   <dc:identifier>https://hdl.handle.net/10630/24784</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>FENS FORUM 2022</dc:relation>
   <dc:relation>PARIS, FRANCIA</dc:relation>
   <dc:relation>9-13 SEPTIEMBRE 2022</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
</oai_dc:dc>
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