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Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses
This study examines the role of autonomic control of maternal and fetal heart rate variability (MHRV and FHRV) and their heartbeats phase coupling prevalence (CP(heartbeat)) in mice. The subjects are divided into three groups: control with saline, cholinergic blockade with atropine, and β-adrenergic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019529/ https://www.ncbi.nlm.nih.gov/pubmed/35188546 http://dx.doi.org/10.1242/bio.058999 |
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author | Khandoker, Ahsan H. Wahbah, Maisam Yoshida, Chihiro Kasahara, Yoshiyuki Funamoto, Kiyoe Niizeki, Kyuichi Kimura, Yoshitaka |
author_facet | Khandoker, Ahsan H. Wahbah, Maisam Yoshida, Chihiro Kasahara, Yoshiyuki Funamoto, Kiyoe Niizeki, Kyuichi Kimura, Yoshitaka |
author_sort | Khandoker, Ahsan H. |
collection | PubMed |
description | This study examines the role of autonomic control of maternal and fetal heart rate variability (MHRV and FHRV) and their heartbeats phase coupling prevalence (CP(heartbeat)) in mice. The subjects are divided into three groups: control with saline, cholinergic blockade with atropine, and β-adrenergic blockade with propranolol. Electrocardiogram signals of 27 anesthetized pregnant mice and 48 fetuses were measured for 20 min (drugs were administered after 10 min). For the coupling analysis, different maternal heartbeats were considered for one fetal beat. Results show that saline infusion did not produce any significant changes in MHRV and FHRV, as well as CP(heartbeat). Atropine increased maternal HR (MHR) and decreased MHRV significantly without any considerable effect on fetal HR (FHR) and FHRV. Propranolol infusion did not produce any significant changes in MHR and MHRV, but significantly decreased FHR and increased FHRV. Moreover, atropine had led to a decrease in CP(heartbeat) when considering two and three maternal beats, and an increase for four beats; while propranolol resulted in a decrease for two heartbeats, but an increase for four and five beats. The proposed approach is useful for assessing the impact of maternal autonomic modulation activity on fetal distress and obstetric complications prevalent in pregnant mothers. |
format | Online Article Text |
id | pubmed-9019529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-90195292022-04-20 Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses Khandoker, Ahsan H. Wahbah, Maisam Yoshida, Chihiro Kasahara, Yoshiyuki Funamoto, Kiyoe Niizeki, Kyuichi Kimura, Yoshitaka Biol Open Research Article This study examines the role of autonomic control of maternal and fetal heart rate variability (MHRV and FHRV) and their heartbeats phase coupling prevalence (CP(heartbeat)) in mice. The subjects are divided into three groups: control with saline, cholinergic blockade with atropine, and β-adrenergic blockade with propranolol. Electrocardiogram signals of 27 anesthetized pregnant mice and 48 fetuses were measured for 20 min (drugs were administered after 10 min). For the coupling analysis, different maternal heartbeats were considered for one fetal beat. Results show that saline infusion did not produce any significant changes in MHRV and FHRV, as well as CP(heartbeat). Atropine increased maternal HR (MHR) and decreased MHRV significantly without any considerable effect on fetal HR (FHR) and FHRV. Propranolol infusion did not produce any significant changes in MHR and MHRV, but significantly decreased FHR and increased FHRV. Moreover, atropine had led to a decrease in CP(heartbeat) when considering two and three maternal beats, and an increase for four beats; while propranolol resulted in a decrease for two heartbeats, but an increase for four and five beats. The proposed approach is useful for assessing the impact of maternal autonomic modulation activity on fetal distress and obstetric complications prevalent in pregnant mothers. The Company of Biologists Ltd 2022-04-13 /pmc/articles/PMC9019529/ /pubmed/35188546 http://dx.doi.org/10.1242/bio.058999 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Khandoker, Ahsan H. Wahbah, Maisam Yoshida, Chihiro Kasahara, Yoshiyuki Funamoto, Kiyoe Niizeki, Kyuichi Kimura, Yoshitaka Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title | Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title_full | Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title_fullStr | Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title_full_unstemmed | Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title_short | Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
title_sort | investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019529/ https://www.ncbi.nlm.nih.gov/pubmed/35188546 http://dx.doi.org/10.1242/bio.058999 |
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