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Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats
Perinatal exposure to adverse experiences disrupts brain development, including the brainstem network that regulates breathing. At adulthood, rats previously subjected to stress (in the form of neonatal maternal separation; NMS) display features reported in patients suffering from sleep disordered b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037225/ https://www.ncbi.nlm.nih.gov/pubmed/27729873 http://dx.doi.org/10.3389/fphys.2016.00432 |
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author | Soliz, Jorge Tam, Rose Kinkead, Richard |
author_facet | Soliz, Jorge Tam, Rose Kinkead, Richard |
author_sort | Soliz, Jorge |
collection | PubMed |
description | Perinatal exposure to adverse experiences disrupts brain development, including the brainstem network that regulates breathing. At adulthood, rats previously subjected to stress (in the form of neonatal maternal separation; NMS) display features reported in patients suffering from sleep disordered breathing, including an increased hypoxic ventilatory response and hypertension. This effect is also sex-specific (males only). Based on these observations, we hypothesized that NMS augments the carotid body's O(2)-chemosensitivity. Using an isolated and perfused ex vivo carotid body preparation from adult rats we compared carotid sinus nerve (CSN) responses to hypoxia and hypercapnia in carotid bodies harvested from adult rats that either experienced control conditions (no experimental manipulation) or were subjected to NMS (3 h/day from postnatal days 3 to 12). In males, the CSN response to hypoxia measured in preparations from NMS males was 1.5 fold higher than controls. In control rats, the female's response was similar to that of males; however, the increase in CSN activity measured in NMS females was 3.0 times lower than controls. The CSN response to hypercapnia was not influenced by stress or sex. We conclude that NMS is sufficient to have persistent and sex-specific effects on the carotid body's response to hypoxia. Because NMS also has sex-specific effects on the neuroendocrine response to stress, we propose that carotid body function is influenced by stress hormones. This, in turn, leads to a predisposition toward cardio-respiratory disorders. |
format | Online Article Text |
id | pubmed-5037225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50372252016-10-11 Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats Soliz, Jorge Tam, Rose Kinkead, Richard Front Physiol Physiology Perinatal exposure to adverse experiences disrupts brain development, including the brainstem network that regulates breathing. At adulthood, rats previously subjected to stress (in the form of neonatal maternal separation; NMS) display features reported in patients suffering from sleep disordered breathing, including an increased hypoxic ventilatory response and hypertension. This effect is also sex-specific (males only). Based on these observations, we hypothesized that NMS augments the carotid body's O(2)-chemosensitivity. Using an isolated and perfused ex vivo carotid body preparation from adult rats we compared carotid sinus nerve (CSN) responses to hypoxia and hypercapnia in carotid bodies harvested from adult rats that either experienced control conditions (no experimental manipulation) or were subjected to NMS (3 h/day from postnatal days 3 to 12). In males, the CSN response to hypoxia measured in preparations from NMS males was 1.5 fold higher than controls. In control rats, the female's response was similar to that of males; however, the increase in CSN activity measured in NMS females was 3.0 times lower than controls. The CSN response to hypercapnia was not influenced by stress or sex. We conclude that NMS is sufficient to have persistent and sex-specific effects on the carotid body's response to hypoxia. Because NMS also has sex-specific effects on the neuroendocrine response to stress, we propose that carotid body function is influenced by stress hormones. This, in turn, leads to a predisposition toward cardio-respiratory disorders. Frontiers Media S.A. 2016-09-27 /pmc/articles/PMC5037225/ /pubmed/27729873 http://dx.doi.org/10.3389/fphys.2016.00432 Text en Copyright © 2016 Soliz, Tam and Kinkead. http://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) or licensor 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 Soliz, Jorge Tam, Rose Kinkead, Richard Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title | Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title_full | Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title_fullStr | Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title_full_unstemmed | Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title_short | Neonatal Maternal Separation Augments Carotid Body Response to Hypoxia in Adult Males but Not Female Rats |
title_sort | neonatal maternal separation augments carotid body response to hypoxia in adult males but not female rats |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037225/ https://www.ncbi.nlm.nih.gov/pubmed/27729873 http://dx.doi.org/10.3389/fphys.2016.00432 |
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