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Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats

BACKGROUND: Intermittent hypoxia induces increased ventilatory responses in a 5-HT-dependent manner. This study aimed to explore that effect of raphe magnus serotonin 1A receptor (5-HT(1A)) receptor on the increased ventilatory responses induced by intermittent hypoxia. METHODS: Stereotaxic surgery...

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Autores principales: Su, Jiao, Meng, Yang, Fang, Yifei, Sun, Linge, Wang, Mengge, Liu, Yanjun, Zhao, Chunling, Dai, Liping, Ouyang, Songyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892800/
https://www.ncbi.nlm.nih.gov/pubmed/35241072
http://dx.doi.org/10.1186/s12931-022-01970-6
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author Su, Jiao
Meng, Yang
Fang, Yifei
Sun, Linge
Wang, Mengge
Liu, Yanjun
Zhao, Chunling
Dai, Liping
Ouyang, Songyun
author_facet Su, Jiao
Meng, Yang
Fang, Yifei
Sun, Linge
Wang, Mengge
Liu, Yanjun
Zhao, Chunling
Dai, Liping
Ouyang, Songyun
author_sort Su, Jiao
collection PubMed
description BACKGROUND: Intermittent hypoxia induces increased ventilatory responses in a 5-HT-dependent manner. This study aimed to explore that effect of raphe magnus serotonin 1A receptor (5-HT(1A)) receptor on the increased ventilatory responses induced by intermittent hypoxia. METHODS: Stereotaxic surgery was performed in adult male rats, and acute and chronic intermittent hypoxia models were established after recovery from surgery. The experimental group received microinjections of 5-HT(1A) receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) into the raphe magnus nucleus (RMg). Meanwhile, the control group received microinjections of artificial cerebrospinal fluid instead of 8-OH-DPAT. Ventilatory responses were compared among the different groups of oxygen status. 5-HT expressions in the RMg region were assessed by immunohistochemistry after chronic intermittent hypoxia. RESULTS: Compared with the normoxia group, the acute intermittent hypoxia group exhibited higher ventilatory responses (e.g., shorter inspiratory time and higher tidal volume, frequency of breathing, minute ventilation, and mean inspiratory flow) (P < 0.05). 8-OH-DPAT microinjection partly weakened these changes in the acute intermittent hypoxia group. Further, compared with the acute intermittent hypoxia group, rats in chronic intermittent hypoxia group exhibited higher measures of ventilatory responses after 1 day of intermittent hypoxia (P < 0.05). These effects peaked after 3 days of intermittent hypoxia treatment and then decreased gradually. Moreover, these changes were diminished in the experimental group. 5-HT expression in the RMg region increased after chronic intermittent hypoxia, which was consistent with the changing trend of ventilatory responses. While activation of the 5-HT(1A) receptor in the RMg region alleviated this phenomenon. CONCLUSIONS: The results indicate that RMg 5-HT(1A) receptor, via changing the expression level of 5-HT in the RMg region, is involved in the modulation of the increased ventilatory responses induced by intermittent hypoxia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-01970-6.
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spelling pubmed-88928002022-03-10 Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats Su, Jiao Meng, Yang Fang, Yifei Sun, Linge Wang, Mengge Liu, Yanjun Zhao, Chunling Dai, Liping Ouyang, Songyun Respir Res Research BACKGROUND: Intermittent hypoxia induces increased ventilatory responses in a 5-HT-dependent manner. This study aimed to explore that effect of raphe magnus serotonin 1A receptor (5-HT(1A)) receptor on the increased ventilatory responses induced by intermittent hypoxia. METHODS: Stereotaxic surgery was performed in adult male rats, and acute and chronic intermittent hypoxia models were established after recovery from surgery. The experimental group received microinjections of 5-HT(1A) receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) into the raphe magnus nucleus (RMg). Meanwhile, the control group received microinjections of artificial cerebrospinal fluid instead of 8-OH-DPAT. Ventilatory responses were compared among the different groups of oxygen status. 5-HT expressions in the RMg region were assessed by immunohistochemistry after chronic intermittent hypoxia. RESULTS: Compared with the normoxia group, the acute intermittent hypoxia group exhibited higher ventilatory responses (e.g., shorter inspiratory time and higher tidal volume, frequency of breathing, minute ventilation, and mean inspiratory flow) (P < 0.05). 8-OH-DPAT microinjection partly weakened these changes in the acute intermittent hypoxia group. Further, compared with the acute intermittent hypoxia group, rats in chronic intermittent hypoxia group exhibited higher measures of ventilatory responses after 1 day of intermittent hypoxia (P < 0.05). These effects peaked after 3 days of intermittent hypoxia treatment and then decreased gradually. Moreover, these changes were diminished in the experimental group. 5-HT expression in the RMg region increased after chronic intermittent hypoxia, which was consistent with the changing trend of ventilatory responses. While activation of the 5-HT(1A) receptor in the RMg region alleviated this phenomenon. CONCLUSIONS: The results indicate that RMg 5-HT(1A) receptor, via changing the expression level of 5-HT in the RMg region, is involved in the modulation of the increased ventilatory responses induced by intermittent hypoxia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-01970-6. BioMed Central 2022-03-03 2022 /pmc/articles/PMC8892800/ /pubmed/35241072 http://dx.doi.org/10.1186/s12931-022-01970-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Su, Jiao
Meng, Yang
Fang, Yifei
Sun, Linge
Wang, Mengge
Liu, Yanjun
Zhao, Chunling
Dai, Liping
Ouyang, Songyun
Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title_full Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title_fullStr Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title_full_unstemmed Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title_short Role of raphe magnus 5-HT(1A) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
title_sort role of raphe magnus 5-ht(1a) receptor in increased ventilatory responses induced by intermittent hypoxia in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892800/
https://www.ncbi.nlm.nih.gov/pubmed/35241072
http://dx.doi.org/10.1186/s12931-022-01970-6
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