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Pharmacological, but not genetic, alteration of neural Epo modifies the CO 2 /H + central chemosensitivity in postnatal mice.
- Source :
-
Respiratory physiology & neurobiology [Respir Physiol Neurobiol] 2017 Aug; Vol. 242, pp. 73-79. Date of Electronic Publication: 2017 Apr 08. - Publication Year :
- 2017
-
Abstract
- Cerebral erythropoietin (Epo) plays a crucial role for respiratory control in newborn rodents. We showed previously that soluble Epo receptor (sEpoR: an Epo antagonist) reduces basal ventilation and hypoxic hyperventilation at postnatal day 10 (P10) and in adult mice. However, at these ages (P10 and adulthood), Epo had no effect on central chemosensitivity. Nevertheless, it is known that the sensitivity to CO <subscript>2</subscript> /H <superscript>+</superscript> during the mammalian respiratory network maturation process is age-dependent. Accordingly, in this study we wanted to test the hypothesis that cerebral Epo is involved in the breathing stimulation induced by the activation of central CO <subscript>2</subscript> /H <superscript>+</superscript> chemoreceptors at earlier postnatal ages. To this end, en bloc brainstem-spinal cord preparations were obtained from P4 mice and the fictive breathing response to CO <subscript>2</subscript> -induced acidosis or metabolic acidosis was analyzed. This age (P4) was chosen because previous research from our laboratory showed that Epo altered (in a dose- and time-dependent manner) the fictive ventilation elicited in brainstem-spinal cord preparations. Moreover, as it was observed that peripheral chemoreceptors determined the respiratory sensitivity of central chemoreceptors to CO <subscript>2</subscript> , the use of this technique restricts our observations to central modulation. Our results did not show differences between preparations from control and transgenic animals (Tg21: overexpressing cerebral Epo; Epo-TAg <superscript>h</superscript> : cerebral Epo deficient mice). However, when Tg21 brainstem preparations were incubated for 1h with sEpoR, or with inhibitors of ERK/Akt (thus blocking the activation of the Epo molecular pathway), the fictive breathing response to CO <subscript>2</subscript> -induced acidosis was blunted. Our data suggest that variation of the Epo/sEpoR ratio is central to breathing modulation during CO <subscript>2</subscript> challenges, and calls attention to clinical perspectives based on the use of Epo drugs at birth in hypoventilation cases.<br /> (Copyright © 2017. Published by Elsevier B.V.)
- Subjects :
- Acidosis metabolism
Animals
Animals, Newborn
Brain Stem drug effects
Erythropoietin antagonists & inhibitors
Erythropoietin genetics
Extracellular Signal-Regulated MAP Kinases antagonists & inhibitors
Extracellular Signal-Regulated MAP Kinases metabolism
Male
Mice, Inbred C57BL
Mice, Transgenic
Proto-Oncogene Proteins c-akt antagonists & inhibitors
Proto-Oncogene Proteins c-akt metabolism
Receptors, Erythropoietin antagonists & inhibitors
Receptors, Erythropoietin metabolism
Respiration drug effects
Spinal Cord drug effects
Tissue Culture Techniques
Brain Stem metabolism
Carbon Dioxide metabolism
Erythropoietin metabolism
Protons
Spinal Cord metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1519
- Volume :
- 242
- Database :
- MEDLINE
- Journal :
- Respiratory physiology & neurobiology
- Publication Type :
- Academic Journal
- Accession number :
- 28396201
- Full Text :
- https://doi.org/10.1016/j.resp.2017.04.003