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Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders

We have recently reported alterations in the plasma concentrations of lysophosphatidic acid (LPA) in patients with substance use disorders. In order to further explore the potential role of the LPA signaling system as biomarker in cocaine use disorders (CUD) we conducted a cross-sectional study with...

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Autores principales: Flores-López, María, García-Marchena, Nuria, Pavón-Morón, Francisco J., Requena-Ocaña, Nerea, Sánchez-Marín, Laura, Martín-Chaves, Laura, García-Medina, Mónica, Pedraza, Carmen, Castilla-Ortega, Estela, Ruiz, Juan J., Rodríguez de Fonseca, Fernando, Araos, Pedro, Serrano, Antonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284796/
https://www.ncbi.nlm.nih.gov/pubmed/37344453
http://dx.doi.org/10.1038/s41398-023-02523-1
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author Flores-López, María
García-Marchena, Nuria
Pavón-Morón, Francisco J.
Requena-Ocaña, Nerea
Sánchez-Marín, Laura
Martín-Chaves, Laura
García-Medina, Mónica
Pedraza, Carmen
Castilla-Ortega, Estela
Ruiz, Juan J.
Rodríguez de Fonseca, Fernando
Araos, Pedro
Serrano, Antonia
author_facet Flores-López, María
García-Marchena, Nuria
Pavón-Morón, Francisco J.
Requena-Ocaña, Nerea
Sánchez-Marín, Laura
Martín-Chaves, Laura
García-Medina, Mónica
Pedraza, Carmen
Castilla-Ortega, Estela
Ruiz, Juan J.
Rodríguez de Fonseca, Fernando
Araos, Pedro
Serrano, Antonia
author_sort Flores-López, María
collection PubMed
description We have recently reported alterations in the plasma concentrations of lysophosphatidic acid (LPA) in patients with substance use disorders. In order to further explore the potential role of the LPA signaling system as biomarker in cocaine use disorders (CUD) we conducted a cross-sectional study with 105 patients diagnosed with CUD and 92 healthy controls. Participants were clinically evaluated and blood samples were collected to determine plasma concentrations of total LPA and LPA species (16:0-, 18:0-, 18:1-, 18:2-, and 20:4-LPA), and the gene expression of LPA(1) and LPA(2) receptors in peripheral blood mononuclear cells. We found that patients with CUD had significantly lower plasma concentration of the majority of LPA species, while the mRNA expression of LPA(1) receptor was found to be higher than controls. Moreover, we found a positive association between plasma concentration of 20:4-LPA and relevant CUD-related variables: age of onset cocaine use and length of cocaine abstinence. The statistical analysis revealed sex differences in concentrations of total LPA and LPA species, and women showed higher LPA concentrations than men. Furthermore, studies in rats of both sexes showed that plasma concentrations of total LPA were also altered after acute and chronic cocaine administration, revealing a sexual dimorphism in these effects. This study found alterations on the LPA signaling system in both, patients with CUD and rats treated with cocaine. Our results demonstrate that LPA signaling is impacted by CUD and sex, which must be taken into consideration in future studies evaluating LPA as a reliable biomarker for CUD.
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spelling pubmed-102847962023-06-23 Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders Flores-López, María García-Marchena, Nuria Pavón-Morón, Francisco J. Requena-Ocaña, Nerea Sánchez-Marín, Laura Martín-Chaves, Laura García-Medina, Mónica Pedraza, Carmen Castilla-Ortega, Estela Ruiz, Juan J. Rodríguez de Fonseca, Fernando Araos, Pedro Serrano, Antonia Transl Psychiatry Article We have recently reported alterations in the plasma concentrations of lysophosphatidic acid (LPA) in patients with substance use disorders. In order to further explore the potential role of the LPA signaling system as biomarker in cocaine use disorders (CUD) we conducted a cross-sectional study with 105 patients diagnosed with CUD and 92 healthy controls. Participants were clinically evaluated and blood samples were collected to determine plasma concentrations of total LPA and LPA species (16:0-, 18:0-, 18:1-, 18:2-, and 20:4-LPA), and the gene expression of LPA(1) and LPA(2) receptors in peripheral blood mononuclear cells. We found that patients with CUD had significantly lower plasma concentration of the majority of LPA species, while the mRNA expression of LPA(1) receptor was found to be higher than controls. Moreover, we found a positive association between plasma concentration of 20:4-LPA and relevant CUD-related variables: age of onset cocaine use and length of cocaine abstinence. The statistical analysis revealed sex differences in concentrations of total LPA and LPA species, and women showed higher LPA concentrations than men. Furthermore, studies in rats of both sexes showed that plasma concentrations of total LPA were also altered after acute and chronic cocaine administration, revealing a sexual dimorphism in these effects. This study found alterations on the LPA signaling system in both, patients with CUD and rats treated with cocaine. Our results demonstrate that LPA signaling is impacted by CUD and sex, which must be taken into consideration in future studies evaluating LPA as a reliable biomarker for CUD. Nature Publishing Group UK 2023-06-21 /pmc/articles/PMC10284796/ /pubmed/37344453 http://dx.doi.org/10.1038/s41398-023-02523-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Flores-López, María
García-Marchena, Nuria
Pavón-Morón, Francisco J.
Requena-Ocaña, Nerea
Sánchez-Marín, Laura
Martín-Chaves, Laura
García-Medina, Mónica
Pedraza, Carmen
Castilla-Ortega, Estela
Ruiz, Juan J.
Rodríguez de Fonseca, Fernando
Araos, Pedro
Serrano, Antonia
Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title_full Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title_fullStr Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title_full_unstemmed Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title_short Plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
title_sort plasma concentrations of lysophosphatidic acid and the expression of its receptors in peripheral blood mononuclear cells are altered in patients with cocaine use disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284796/
https://www.ncbi.nlm.nih.gov/pubmed/37344453
http://dx.doi.org/10.1038/s41398-023-02523-1
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