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Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice

We recently showed that blunt chest trauma reduced the expression of the myocardial oxytocin receptor (Oxtr), which was further aggravated by genetic deletion of the H(2)S-producing enzyme cystathionine γ-lyase (CSE). Exogenous H(2)S supplementation restored myocardial Oxtr expression under these co...

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Autores principales: Wigger, Daniela C., Gröger, Nicole, Lesse, Alexandra, Krause, Sabrina, Merz, Tamara, Gündel, Harald, Braun, Katharina, McCook, Oscar, Radermacher, Peter, Bock, Jörg, Waller, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007946/
https://www.ncbi.nlm.nih.gov/pubmed/32082478
http://dx.doi.org/10.1155/2020/4309605
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author Wigger, Daniela C.
Gröger, Nicole
Lesse, Alexandra
Krause, Sabrina
Merz, Tamara
Gündel, Harald
Braun, Katharina
McCook, Oscar
Radermacher, Peter
Bock, Jörg
Waller, Christiane
author_facet Wigger, Daniela C.
Gröger, Nicole
Lesse, Alexandra
Krause, Sabrina
Merz, Tamara
Gündel, Harald
Braun, Katharina
McCook, Oscar
Radermacher, Peter
Bock, Jörg
Waller, Christiane
author_sort Wigger, Daniela C.
collection PubMed
description We recently showed that blunt chest trauma reduced the expression of the myocardial oxytocin receptor (Oxtr), which was further aggravated by genetic deletion of the H(2)S-producing enzyme cystathionine γ-lyase (CSE). Exogenous H(2)S supplementation restored myocardial Oxtr expression under these conditions. Early life stress (ELS) is a risk factor for cardiovascular disease by affecting vascular and heart structures. Therefore, we tested the hypotheses that (i) ELS affects cardiac Oxtr and CSE expressions and (ii) Oxtr and CSE expression patterns depend on the duration of stress exposure. Thus, two stress paradigms were compared: long- and short-term separation stress (LTSS and STSS, respectively). Cardiac Oxtr expression was differentially affected by the two stress paradigms with a significant reduction after LTSS and a significant increase after STSS. CSE expression, which was significantly reduced in Oxtr(−/−) knockout hearts, was downregulated and directly related to Oxtr expression in LTSS hearts (r = 0.657, p = 0.012). In contrast, CSE expression was not related to Oxtr upregulation in STSS. Plasma Oxt levels were not affected by either ELS paradigm. The coincidence of LTSS-induced reduction of cardiac Oxtr and reduced CSE expression may suggest a novel pathophysiological link between early life adversities and increased risk for the development of cardiovascular disorders in adulthood.
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spelling pubmed-70079462020-02-20 Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice Wigger, Daniela C. Gröger, Nicole Lesse, Alexandra Krause, Sabrina Merz, Tamara Gündel, Harald Braun, Katharina McCook, Oscar Radermacher, Peter Bock, Jörg Waller, Christiane Oxid Med Cell Longev Research Article We recently showed that blunt chest trauma reduced the expression of the myocardial oxytocin receptor (Oxtr), which was further aggravated by genetic deletion of the H(2)S-producing enzyme cystathionine γ-lyase (CSE). Exogenous H(2)S supplementation restored myocardial Oxtr expression under these conditions. Early life stress (ELS) is a risk factor for cardiovascular disease by affecting vascular and heart structures. Therefore, we tested the hypotheses that (i) ELS affects cardiac Oxtr and CSE expressions and (ii) Oxtr and CSE expression patterns depend on the duration of stress exposure. Thus, two stress paradigms were compared: long- and short-term separation stress (LTSS and STSS, respectively). Cardiac Oxtr expression was differentially affected by the two stress paradigms with a significant reduction after LTSS and a significant increase after STSS. CSE expression, which was significantly reduced in Oxtr(−/−) knockout hearts, was downregulated and directly related to Oxtr expression in LTSS hearts (r = 0.657, p = 0.012). In contrast, CSE expression was not related to Oxtr upregulation in STSS. Plasma Oxt levels were not affected by either ELS paradigm. The coincidence of LTSS-induced reduction of cardiac Oxtr and reduced CSE expression may suggest a novel pathophysiological link between early life adversities and increased risk for the development of cardiovascular disorders in adulthood. Hindawi 2020-01-24 /pmc/articles/PMC7007946/ /pubmed/32082478 http://dx.doi.org/10.1155/2020/4309605 Text en Copyright © 2020 Daniela C. Wigger et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wigger, Daniela C.
Gröger, Nicole
Lesse, Alexandra
Krause, Sabrina
Merz, Tamara
Gündel, Harald
Braun, Katharina
McCook, Oscar
Radermacher, Peter
Bock, Jörg
Waller, Christiane
Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title_full Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title_fullStr Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title_full_unstemmed Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title_short Maternal Separation Induces Long-Term Alterations in the Cardiac Oxytocin Receptor and Cystathionine γ-Lyase Expression in Mice
title_sort maternal separation induces long-term alterations in the cardiac oxytocin receptor and cystathionine γ-lyase expression in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007946/
https://www.ncbi.nlm.nih.gov/pubmed/32082478
http://dx.doi.org/10.1155/2020/4309605
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