» Articles » PMID: 10949066

Physiological Basis for Human Autonomic Rhythms

Overview
Journal Ann Med
Publisher Informa Healthcare
Specialty General Medicine
Date 2000 Aug 19
PMID 10949066
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Oscillations of arterial pressures, heart periods, and muscle sympathetic nerve activity have been studied intensively in recent years to explore otherwise obscure human neurophysiological mechanisms. The best-studied rhythms are those occurring at breathing frequencies. Published evidence indicates that respiratory fluctuations of muscle sympathetic nerve activity and electrocardiographic R-R intervals result primarily from the action of a central 'gate' that opens during expiration and closes during inspiration. Parallel respiratory fluctuations of arterial pressures and R-R intervals are thought to be secondary to arterial baroreflex physiology: changes in systolic pressure provoke changes in the R-R interval. However, growing evidence suggests that these parallel oscillations result from the influence of respiration on sympathetic and vagal-cardiac motoneurones rather than from baroreflex physiology. There is a rapidly growing literature on the use of mathematical models of low- and high-frequency (respiratory) R-R interval fluctuations in characterizing instantaneous 'sympathovagal balance'. The case for this approach is based primarily on measurements made with patients in upright tilt. However, the strong linear relation between such measures as the ratio of low- to high-frequency R-R interval oscillations and the angle of the tilt reflects exclusively the reductions of the vagal (high-frequency) component. As the sympathetic component does not change in tilt, the low- to high-frequency R-R interval ratio provides no proof that sympathetic activity increases. Moreover, the validity of extrapolating from measurements performed during upright tilt to measurements during supine rest has not been established. Nonetheless, it is clear that measures of heart rate variability provide important prognostic information in patients with cardiovascular diseases. It is not known whether reduced heart rate variability is merely a marker for the severity of disease or a measurement that identifies functional reflex abnormalities contributing to terminal dysrhythmias.

Citing Articles

The contribution of granger causality analysis to our understanding of cardiovascular homeostasis: from cardiovascular and respiratory interactions to central autonomic network control.

Pichot V, Corbier C, Chouchou F Front Netw Physiol. 2024; 4:1315316.

PMID: 39175608 PMC: 11338816. DOI: 10.3389/fnetp.2024.1315316.


Publication guidelines for human heart rate and heart rate variability studies in psychophysiology-Part 1: Physiological underpinnings and foundations of measurement.

Quigley K, Gianaros P, Norman G, Jennings J, Berntson G, de Geus E Psychophysiology. 2024; 61(9):e14604.

PMID: 38873876 PMC: 11539922. DOI: 10.1111/psyp.14604.


Tilt-evoked, breathing-driven blood pressure oscillations: Independence from baroreflex-sympathoneural function.

Grabov E, Sullivan P, Wang S, Goldstein D Clin Auton Res. 2024; 34(1):125-135.

PMID: 38446362 PMC: 10944440. DOI: 10.1007/s10286-024-01022-7.


The frequency of atrial fibrillatory waves is modulated by the spatiotemporal pattern of acetylcholine release: a 3D computational study.

Celotto C, Sanchez C, Abdollahpur M, Sandberg F, Rodriguez Mstas J, Laguna P Front Physiol. 2024; 14:1189464.

PMID: 38235381 PMC: 10791938. DOI: 10.3389/fphys.2023.1189464.


Accuracy and reliability of the optoelectronic plethysmography and the heart rate systems for measuring breathing rates compared with the spirometer.

Stubbe L, Houel N, Cottin F Sci Rep. 2022; 12(1):19255.

PMID: 36357452 PMC: 9648890. DOI: 10.1038/s41598-022-23915-1.