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In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata
Erythropoietin (Epo) and its receptor are expressed in central respiratory areas. We hypothesized that chronic Epo deficiency alters functioning of central respiratory areas and thus the respiratory adaptation to hypercapnia. The hypercapnic ventilatory response (HcVR) was evaluated by whole body pl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061944/ https://www.ncbi.nlm.nih.gov/pubmed/35514353 http://dx.doi.org/10.3389/fphys.2022.850418 |
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author | Jeton, Florine Perrin-Terrin, Anne-Sophie Yegen, Celine-Hivda Marchant, Dominique Richalet, Jean-Paul Pichon, Aurélien Boncoeur, Emilie Bodineau, Laurence Voituron, Nicolas |
author_facet | Jeton, Florine Perrin-Terrin, Anne-Sophie Yegen, Celine-Hivda Marchant, Dominique Richalet, Jean-Paul Pichon, Aurélien Boncoeur, Emilie Bodineau, Laurence Voituron, Nicolas |
author_sort | Jeton, Florine |
collection | PubMed |
description | Erythropoietin (Epo) and its receptor are expressed in central respiratory areas. We hypothesized that chronic Epo deficiency alters functioning of central respiratory areas and thus the respiratory adaptation to hypercapnia. The hypercapnic ventilatory response (HcVR) was evaluated by whole body plethysmography in wild type (WT) and Epo deficient (Epo-TAg(h)) adult male mice under 4%CO(2). Epo-TAg(h) mice showed a larger HcVR than WT mice because of an increase in both respiratory frequency and tidal volume, whereas WT mice only increased their tidal volume. A functional histological approach revealed changes in CO(2)/H(+)-activated cells between Epo-TAg(h) and WT mice. First, Epo-TAg(h) mice showed a smaller increase under hypercapnia in c-FOS-positive number of cells in the retrotrapezoid nucleus/parafacial respiratory group than WT, and this, independently of changes in the number of PHOX2B-expressing cells. Second, we did not observe in Epo-TAg(h) mice the hypercapnic increase in c-FOS-positive number of cells in the nucleus of the solitary tract present in WT mice. Finally, whereas hypercapnia did not induce an increase in the c-FOS-positive number of cells in medullary raphe nuclei in WT mice, chronic Epo deficiency leads to raphe pallidus and magnus nuclei activation by hyperacpnia, with a significant part of c-FOS positive cells displaying an immunoreactivity for serotonin in the raphe pallidus nucleus. All of these results suggest that chronic Epo-deficiency affects both the pattern of ventilatory response to hypercapnia and associated medullary respiratory network at adult stage with an increase in the sensitivity of 5-HT and non-5-HT neurons of the raphe medullary nuclei leading to stimulation of f (R) for moderate level of CO(2). |
format | Online Article Text |
id | pubmed-9061944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90619442022-05-04 In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata Jeton, Florine Perrin-Terrin, Anne-Sophie Yegen, Celine-Hivda Marchant, Dominique Richalet, Jean-Paul Pichon, Aurélien Boncoeur, Emilie Bodineau, Laurence Voituron, Nicolas Front Physiol Physiology Erythropoietin (Epo) and its receptor are expressed in central respiratory areas. We hypothesized that chronic Epo deficiency alters functioning of central respiratory areas and thus the respiratory adaptation to hypercapnia. The hypercapnic ventilatory response (HcVR) was evaluated by whole body plethysmography in wild type (WT) and Epo deficient (Epo-TAg(h)) adult male mice under 4%CO(2). Epo-TAg(h) mice showed a larger HcVR than WT mice because of an increase in both respiratory frequency and tidal volume, whereas WT mice only increased their tidal volume. A functional histological approach revealed changes in CO(2)/H(+)-activated cells between Epo-TAg(h) and WT mice. First, Epo-TAg(h) mice showed a smaller increase under hypercapnia in c-FOS-positive number of cells in the retrotrapezoid nucleus/parafacial respiratory group than WT, and this, independently of changes in the number of PHOX2B-expressing cells. Second, we did not observe in Epo-TAg(h) mice the hypercapnic increase in c-FOS-positive number of cells in the nucleus of the solitary tract present in WT mice. Finally, whereas hypercapnia did not induce an increase in the c-FOS-positive number of cells in medullary raphe nuclei in WT mice, chronic Epo deficiency leads to raphe pallidus and magnus nuclei activation by hyperacpnia, with a significant part of c-FOS positive cells displaying an immunoreactivity for serotonin in the raphe pallidus nucleus. All of these results suggest that chronic Epo-deficiency affects both the pattern of ventilatory response to hypercapnia and associated medullary respiratory network at adult stage with an increase in the sensitivity of 5-HT and non-5-HT neurons of the raphe medullary nuclei leading to stimulation of f (R) for moderate level of CO(2). Frontiers Media S.A. 2022-04-19 /pmc/articles/PMC9061944/ /pubmed/35514353 http://dx.doi.org/10.3389/fphys.2022.850418 Text en Copyright © 2022 Jeton, Perrin-Terrin, Yegen, Marchant, Richalet, Pichon, Boncoeur, Bodineau and Voituron. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Jeton, Florine Perrin-Terrin, Anne-Sophie Yegen, Celine-Hivda Marchant, Dominique Richalet, Jean-Paul Pichon, Aurélien Boncoeur, Emilie Bodineau, Laurence Voituron, Nicolas In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title | In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title_full | In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title_fullStr | In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title_full_unstemmed | In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title_short | In Transgenic Erythropoietin Deficient Mice, an Increase in Respiratory Response to Hypercapnia Parallels Abnormal Distribution of CO(2)/H(+)-Activated Cells in the Medulla Oblongata |
title_sort | in transgenic erythropoietin deficient mice, an increase in respiratory response to hypercapnia parallels abnormal distribution of co(2)/h(+)-activated cells in the medulla oblongata |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061944/ https://www.ncbi.nlm.nih.gov/pubmed/35514353 http://dx.doi.org/10.3389/fphys.2022.850418 |
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