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      <dc:title>What role does the LPA1 receptor play in regulating emotional-like behaviours?</dc:title>
      <dc:creator>Pedraza-Sánchez-López, J.</dc:creator>
      <dc:creator>Castilla-Ortega, María Estela</dc:creator>
      <dc:creator>Rosell-del-Valle, Cristina</dc:creator>
      <dc:creator>Moreno-Fernández, Román D.</dc:creator>
      <dc:creator>Zambrana-Infantes, Emma</dc:creator>
      <dc:creator>García-Fernández, María Inmaculada</dc:creator>
      <dc:creator>Rodriguez-de-Fonseca, Fernando</dc:creator>
      <dc:creator>Chun, Jerold</dc:creator>
      <dc:creator>Estivill-Torrús, Guillermo</dc:creator>
      <dc:creator>Santín-Núñez, Luis Javier</dc:creator>
      <dc:subject>Emociones</dc:subject>
      <dc:subject>Ansiedad</dc:subject>
      <dc:description>The LPA1 receptor is one of the six characterized G protein-coupled receptors (LPA1–6)&#xd;
through which lysophosphatidic acid acts as an intercellular signalling molecule. It has been&#xd;
proposed that this receptor has a role in controlling anxiety-like behaviours and in the&#xd;
detrimental consequences of stress. In general, the neurobiological mechanism of fear extinction&#xd;
is strikingly similar to that of the adaptative stress response (distress regulation), sharing similar&#xd;
neuroanatomical, neuroendocrine, and neurochemical basis. Inadequate control of the stress&#xd;
response could precipitate or provoke anxiety disorders. In this context, we tried to elucidate the&#xd;
LPA1 receptor involvement in emotional regulation. For this purpose, we first examined fear&#xd;
extinction, a type of emotional regulation, in normal wild-type (wt) and maLPA1-null mice&#xd;
using two different extinction procedures (cued fear extinction and contextual fear extinction).&#xd;
Additionally, to study the role of the LPA1 receptor in the absence of developmental&#xd;
abnormalities induced by its permanent loss, the effect of the LPA1 antagonist Ki16425&#xd;
administration was examined in contextual fear extinction on wild-type mice. Next, we studied&#xd;
the consequences of the absence of the LPA1 receptor in two key areas involved in emotional&#xd;
regulation, characterizing the structure and GABAergic composition of the medial prefrontal&#xd;
cortex (mPFC) and the amygdala by immunohistochemical detection of neuron specific nuclear&#xd;
protein (NeuN), GABA-positive cells and calcium-binding proteins (calretinin (CR),&#xd;
parvalbumin (PV), and calbindin (CB)). Lastly, we examined the corticosterone response and&#xd;
the expression of a marker of neuronal activity, c-Fos protein, in the amygdala and the mPFC&#xd;
after acute stress. Our results revealed that lack of the LPA1-receptor induces exaggerated&#xd;
amygdala reactivity and endocrine responses to emotional stimuli (e.g., an acute episode of&#xd;
stress), revealing a role of the LPA1 receptor in regulating emotional-like behaviours.&#xd;
Considering that a reduction of GABAergic inhibitory control in the amygdala may be a&#xd;
common mechanism to generate a heightened emotional state, the abnormal emotional response&#xd;
reported in LPA1-null mice could be explained, at least in part, by a significant reduction of&#xd;
GABAérgic composition of the amygdala observed in these animals.&#xd;
Taking together, the LPA1 receptor is involved in emotional behaviours and in the anatomical&#xd;
integrity of the corticolimbic circuit, the deregulation of which may be a susceptibility factor for anxiety disorders and a potential therapeutic target for the treatment of these diseases.</dc:description>
      <dc:date>2015-07-24T11:50:30Z</dc:date>
      <dc:date>2015-07-24T11:50:30Z</dc:date>
      <dc:date>2015</dc:date>
      <dc:date>2015-07-24</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>http://hdl.handle.net/10630/10153</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>I IInternational Congress of Psychobiology</dc:relation>
      <dc:relation>Oviedo</dc:relation>
      <dc:relation>Julio 2015</dc:relation>
      <dc:rights>open access</dc:rights>
      <dc:rights>by-nc-nd</dc:rights>
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