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1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats
The role of lysophosphatidic acid (LPA) in the control of emotional behavior remains to be determined. We analyzed the effects of the central administration of 1-oleoyl-LPA (LPA 18∶1) in rats tested for food consumption and anxiety-like and depression-like behaviors. For this purpose, the elevated p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883702/ https://www.ncbi.nlm.nih.gov/pubmed/24409327 http://dx.doi.org/10.1371/journal.pone.0085348 |
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author | Castilla-Ortega, Estela Escuredo, Leticia Bilbao, Ainhoa Pedraza, Carmen Orio, Laura Estivill-Torrús, Guillermo Santín, Luis J. de Fonseca, Fernando Rodríguez Pavón, Francisco Javier |
author_facet | Castilla-Ortega, Estela Escuredo, Leticia Bilbao, Ainhoa Pedraza, Carmen Orio, Laura Estivill-Torrús, Guillermo Santín, Luis J. de Fonseca, Fernando Rodríguez Pavón, Francisco Javier |
author_sort | Castilla-Ortega, Estela |
collection | PubMed |
description | The role of lysophosphatidic acid (LPA) in the control of emotional behavior remains to be determined. We analyzed the effects of the central administration of 1-oleoyl-LPA (LPA 18∶1) in rats tested for food consumption and anxiety-like and depression-like behaviors. For this purpose, the elevated plus-maze, open field, Y maze, forced swimming and food intake tests were performed. In addition, c-Fos expression in the dorsal periaqueductal gray matter (DPAG) was also determined. The results revealed that the administration of LPA 18∶1 reduced the time in the open arms of the elevated plus-maze and induced hypolocomotion in the open field, suggesting an anxiogenic-like phenotype. Interestingly, these effects were present following LPA 18∶1 infusion under conditions of novelty but not under habituation conditions. In the forced swimming test, the administration of LPA 18∶1 dose-dependently increased depression-like behavior, as evaluated according to immobility time. LPA treatment induced no effects on feeding. However, the immunohistochemical analysis revealed that LPA 18∶1 increased c-Fos expression in the DPAG. The abundant expression of the LPA(1) receptor, one of the main targets for LPA 18∶1, was detected in this brain area, which participates in the control of emotional behavior, using immunocytochemistry. These findings indicate that LPA is a relevant transmitter potentially involved in normal and pathological emotional responses, including anxiety and depression. |
format | Online Article Text |
id | pubmed-3883702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38837022014-01-09 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats Castilla-Ortega, Estela Escuredo, Leticia Bilbao, Ainhoa Pedraza, Carmen Orio, Laura Estivill-Torrús, Guillermo Santín, Luis J. de Fonseca, Fernando Rodríguez Pavón, Francisco Javier PLoS One Research Article The role of lysophosphatidic acid (LPA) in the control of emotional behavior remains to be determined. We analyzed the effects of the central administration of 1-oleoyl-LPA (LPA 18∶1) in rats tested for food consumption and anxiety-like and depression-like behaviors. For this purpose, the elevated plus-maze, open field, Y maze, forced swimming and food intake tests were performed. In addition, c-Fos expression in the dorsal periaqueductal gray matter (DPAG) was also determined. The results revealed that the administration of LPA 18∶1 reduced the time in the open arms of the elevated plus-maze and induced hypolocomotion in the open field, suggesting an anxiogenic-like phenotype. Interestingly, these effects were present following LPA 18∶1 infusion under conditions of novelty but not under habituation conditions. In the forced swimming test, the administration of LPA 18∶1 dose-dependently increased depression-like behavior, as evaluated according to immobility time. LPA treatment induced no effects on feeding. However, the immunohistochemical analysis revealed that LPA 18∶1 increased c-Fos expression in the DPAG. The abundant expression of the LPA(1) receptor, one of the main targets for LPA 18∶1, was detected in this brain area, which participates in the control of emotional behavior, using immunocytochemistry. These findings indicate that LPA is a relevant transmitter potentially involved in normal and pathological emotional responses, including anxiety and depression. Public Library of Science 2014-01-07 /pmc/articles/PMC3883702/ /pubmed/24409327 http://dx.doi.org/10.1371/journal.pone.0085348 Text en © 2014 Castilla-Ortega et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Castilla-Ortega, Estela Escuredo, Leticia Bilbao, Ainhoa Pedraza, Carmen Orio, Laura Estivill-Torrús, Guillermo Santín, Luis J. de Fonseca, Fernando Rodríguez Pavón, Francisco Javier 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title | 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title_full | 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title_fullStr | 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title_full_unstemmed | 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title_short | 1-Oleoyl Lysophosphatidic Acid: A New Mediator of Emotional Behavior in Rats |
title_sort | 1-oleoyl lysophosphatidic acid: a new mediator of emotional behavior in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883702/ https://www.ncbi.nlm.nih.gov/pubmed/24409327 http://dx.doi.org/10.1371/journal.pone.0085348 |
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