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性别和呼吸途径会调节人类的心肺变异性。

Gender and breathing route modulate cardio-respiratory variability in humans.

作者信息

Busha Brett F, Hage Erik, Hofmann Cory

机构信息

Department of Electrical and Computer Engineering, The College of New Jersey, NJ 08628, United States.

出版信息

Respir Physiol Neurobiol. 2009 Apr 30;166(2):87-94. doi: 10.1016/j.resp.2009.02.008. Epub 2009 Feb 26.

Abstract

During spontaneous breathing, there is an intrinsic scaling of respiratory variability and a correlation between respiratory and heart rate variabilities. To identify the effect of breathing route on respiratory and heart rate variabilities, breath-to-breath interval (BBI) and heartbeat-to-heartbeat interval (RRI) were recorded from 12 female and 12 male adult subjects breathing through the nose or mouth. Temporal scaling within the BBI and RRI was quantified with detrended fluctuation analysis (DFA). We identified a significant gender-based breathing route interaction in the short-term scaling of BBI (p=0.007), a decrease in the short-term scaling of RRI during nose breathing (p=0.026), and a significant interdependence of short-term scaling of BBI and RRI in female subjects. We conclude that there is a gender-based differential effect of breathing route on the control of respiration and an increase in the random behavior of RRI associated with nasal breathing. These data also suggest the presence cardio-respiratory coupling of scaling behavior in female subjects.

摘要

在自主呼吸过程中,呼吸变异性存在内在标度,且呼吸变异性与心率变异性之间存在相关性。为了确定呼吸途径对呼吸和心率变异性的影响,记录了12名成年女性和12名成年男性通过鼻或口呼吸时的逐次呼吸间隔(BBI)和逐次心跳间隔(RRI)。采用去趋势波动分析(DFA)对BBI和RRI内的时间标度进行量化。我们发现在BBI的短期标度中存在基于性别的呼吸途径交互作用(p = 0.007),在鼻呼吸期间RRI的短期标度降低(p = 0.026),并且在女性受试者中BBI和RRI的短期标度存在显著的相互依赖性。我们得出结论,呼吸途径对呼吸控制存在基于性别的差异效应,并且与鼻呼吸相关的RRI随机行为增加。这些数据还表明女性受试者中存在标度行为的心肺耦合。

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