4.3 Article

Investigating the effect of cholinergic and adrenergic blocking agents on maternal-fetal heart rates and their interactions in mice fetuses

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BIOLOGY OPEN
卷 11, 期 4, 页码 -

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COMPANY BIOLOGISTS LTD
DOI: 10.1242/bio.058999

关键词

Autonomic regulation; Autonomic blockade; Fetal and maternal heart rate; Heart rate variability; Pregnant mice

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资金

  1. Khalifa University, Abu Dhabi, United Arab Emirates [CIRA 2019-023, 8474000174]
  2. KAKENHI, Japan [20K09590]
  3. Creative Interdisciplinary Research Project of Frontier Research Institute for Interdisciplinary Science, Tohoku University
  4. Khalifa University of Science and Technology
  5. Grants-in-Aid for Scientific Research [20K09590] Funding Source: KAKEN

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This study examines the role of autonomic control in the variability of maternal and fetal heart rates, as well as the prevalence of heartbeats phase coupling in mice. The results show that atropine and propranolol have different effects on maternal and fetal heart rates, and the number of heartbeats considered also affects the phase coupling. This approach may be important for evaluating the impact of maternal autonomic regulation on fetal health and obstetric complications.
This study examines the role of autonomic control of maternal and fetal heart rate variability (MHRV and FHRV) and their heartbeats phase coupling prevalence (CPheartbeat) in mice. The subjects are divided into three groups: control with saline, cholinergic blockade with atropine, and beta-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 CPheartbeat. 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 CPheartbeat 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.

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