Why the study?
Does paced breathing and its respiratory interval modify the relationship between spectral components of heart rate variability and cardiac vagal tone in healthy young males?
Does paced breathing and its respiratory interval modify the relationship between spectral components of heart rate variability and cardiac vagal tone in healthy young males?
Increased respiratory intervals during paced breathing amplify respiratory-related vagal modulation of heart rate without changing mean cardiac vagal tone.
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Longer respiratory intervals amplify HF-HRV amplitude without changing mean R-R; hypothesis-generating for paced breathing standardization in vagal assessment.
To determine whether paced breathing (PB) and respiratory interval of PB modify the relationship between spectral components of heart rate variability (HRV) and cardiac vagal tone, we studied seven healthy young males under the condition of beta-adrenergic blockade by intravenous propranolol (0.2 mg/kg). Compared with spontaneous breathing, PB at the same respiratory interval as that of individual spontaneous breathing showed no significant effect on the amplitude of the high-frequency (HF) component or the mean R-R interval in either the supine or tilt position, whereas the PB decreased the amplitude of the low-frequency (LF; 0.04-0.15 Hz) component in both positions (P = 0.004 and 0.042, respectively). When the respiratory interval was increased from 3 to 6 s, the HF amplitude showed a progressive increase in both positions (P = 0.001 and 0.035, respectively), while the LF amplitude and mean R-R interval remained unchanged. These results indicate that the effects of PB and respiratory interval on the spectral components of HRV are not mediated by the changes in mean cardiac vagal tone and support the hypothesis that increased respiratory interval amplifies the respiratory-related vagal modulation of heart rate.
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Hayano et al. (1994) studied this question.
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