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Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats
The purpose of this study is to examine the influence of acute progressive hypoxia on cardiovascular variability and striatal dopamine (DA) levels in conscious, spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY). After preparation for measurement, the inspired oxygen concentration of...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941824/ https://www.ncbi.nlm.nih.gov/pubmed/18599365 http://dx.doi.org/10.1016/j.autneu.2008.05.008 |
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author | Sugimura, Mitsutaka Hirose, Yohsuke Hanamoto, Hiroshi Okada, Kenji Boku, Aiji Morimoto, Yoshinari Taki, Kunitaka Niwa, Hitoshi |
author_facet | Sugimura, Mitsutaka Hirose, Yohsuke Hanamoto, Hiroshi Okada, Kenji Boku, Aiji Morimoto, Yoshinari Taki, Kunitaka Niwa, Hitoshi |
author_sort | Sugimura, Mitsutaka |
collection | PubMed |
description | The purpose of this study is to examine the influence of acute progressive hypoxia on cardiovascular variability and striatal dopamine (DA) levels in conscious, spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY). After preparation for measurement, the inspired oxygen concentration of rats was decreased to 10% within 5 min (descent stage), maintained at 10% for 10 min (fixed stage), and then elevated back to 20% over 5 min (recovery stage). The systolic blood pressure (SBP) and heart rate (HR) variability at each stage was calculated to evaluate the autonomic nervous system response using the wavelet method. Striatal DA during each stage was measured using in vivo microdialysis. We found that SHR showed a more profound hemodynamic response to progressive hypoxia as compared to WKY. Cardiac parasympathetic activity in SHR was significantly inhibited by acute progressive hypoxia during all stages, as shown by the decrease in the high frequency band of HR variability (HR-HF), along with transient increase in sympathetic activity during the early hypoxic phase. This decrease in the HR-HF continued even when SBP was elevated. Striatal DA levels showed the transient similar elevation in both groups. These findings suggest that acute progressive hypoxic stress in SHR inhibits cardiac parasympathetic activity through reduction of baroreceptor reflex sensitivity, with potentially severe deleterious effects on circulation, in particular on HR and circulatory control. Furthermore, it is thought that the influence of acute progressive hypoxia on striatal DA levels is similar in SHR and WKY. |
format | Text |
id | pubmed-2941824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-29418242010-10-21 Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats Sugimura, Mitsutaka Hirose, Yohsuke Hanamoto, Hiroshi Okada, Kenji Boku, Aiji Morimoto, Yoshinari Taki, Kunitaka Niwa, Hitoshi Auton Neurosci Article The purpose of this study is to examine the influence of acute progressive hypoxia on cardiovascular variability and striatal dopamine (DA) levels in conscious, spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY). After preparation for measurement, the inspired oxygen concentration of rats was decreased to 10% within 5 min (descent stage), maintained at 10% for 10 min (fixed stage), and then elevated back to 20% over 5 min (recovery stage). The systolic blood pressure (SBP) and heart rate (HR) variability at each stage was calculated to evaluate the autonomic nervous system response using the wavelet method. Striatal DA during each stage was measured using in vivo microdialysis. We found that SHR showed a more profound hemodynamic response to progressive hypoxia as compared to WKY. Cardiac parasympathetic activity in SHR was significantly inhibited by acute progressive hypoxia during all stages, as shown by the decrease in the high frequency band of HR variability (HR-HF), along with transient increase in sympathetic activity during the early hypoxic phase. This decrease in the HR-HF continued even when SBP was elevated. Striatal DA levels showed the transient similar elevation in both groups. These findings suggest that acute progressive hypoxic stress in SHR inhibits cardiac parasympathetic activity through reduction of baroreceptor reflex sensitivity, with potentially severe deleterious effects on circulation, in particular on HR and circulatory control. Furthermore, it is thought that the influence of acute progressive hypoxia on striatal DA levels is similar in SHR and WKY. Elsevier 2008-08-18 /pmc/articles/PMC2941824/ /pubmed/18599365 http://dx.doi.org/10.1016/j.autneu.2008.05.008 Text en © 2008 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Sugimura, Mitsutaka Hirose, Yohsuke Hanamoto, Hiroshi Okada, Kenji Boku, Aiji Morimoto, Yoshinari Taki, Kunitaka Niwa, Hitoshi Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title | Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title_full | Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title_fullStr | Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title_full_unstemmed | Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title_short | Influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
title_sort | influence of acute progressive hypoxia on cardiovascular variability in conscious spontaneously hypertensive rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941824/ https://www.ncbi.nlm.nih.gov/pubmed/18599365 http://dx.doi.org/10.1016/j.autneu.2008.05.008 |
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