» Articles » PMID: 29604069

Moderate and Severe Hypoxia Elicit Divergent Effects on Cardiovascular Function and Physiological Rhythms

Overview
Journal J Physiol
Specialty Physiology
Date 2018 Apr 1
PMID 29604069
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Key Points: In the present study, we provide evidence for divergent physiological responses to moderate compared to severe hypoxia, addressing an important knowledge gap related to severity, duration and after-effects of hypoxia encountered in cardiopulmonary situations. The physiological responses to moderate and severe hypoxia were not proportional, linear or concurrent with the time-of-day. Hypoxia elicited severity-dependent physiological responses that either persisted or fluctuated throughout normoxic recovery. The physiological basis for these distinct cardiovascular responses implicates a shift in the sympathovagal set point and probably not molecular changes at the artery resulting from hypoxic stress.

Abstract: Hypoxia is both a consequence and cause of many acute and chronic diseases. Severe hypoxia causes hypertension with cardiovascular sequelae; however, the rare studies using moderate severities of hypoxia indicate that it can be beneficial, suggesting that hypoxia may not always be detrimental. Comparisons between studies are difficult because of the varied classifications of hypoxic severities, methods of delivery and use of anaesthetics. Thus, to investigate the long-term effects of moderate hypoxia on cardiovascular health, radiotelemetry was used to obtain in vivo physiological measurements in unanaesthetized mice during 24 h of either moderate or severe hypoxia, followed by 72 h of normoxic recovery. Systolic blood pressure was decreased during recovery following moderate hypoxia but increased following severe hypoxia. Moderate and severe hypoxia increased haeme oxygenase-1 expression during recovery, suggesting parity in hypoxic stress at the level of the artery. Severe but not moderate hypoxia increased the low/high frequency ratio of heart rate variability 72 h post-hypoxia, indicating a shift in sympathovagal balance. Moderate hypoxia dampened the amplitude of circadian rhythm, whereas severe disrupted rhythm during the entire insult, with perturbations persisting throughout normoxic recovery. Thus, hypoxic severity differentially regulates circadian blood pressure.

Citing Articles

Dose-effect of exercise intervention on heart rate variability of acclimatized young male lowlanders at 3,680 m.

Su R, Peng P, Zhang W, Huang J, Fan J, Zhang D Front Physiol. 2024; 15:1331693.

PMID: 38606008 PMC: 11007668. DOI: 10.3389/fphys.2024.1331693.


Hypoxia-induced inflammation: Profiling the first 24-hour posthypoxic plasma and central nervous system changes.

Mesentier-Louro L, Rangel B, Stell L, Shariati M, Dalal R, Nathan A PLoS One. 2021; 16(3):e0246681.

PMID: 33661927 PMC: 7932147. DOI: 10.1371/journal.pone.0246681.


Disruption of Physiological Rhythms Persist Following Cessation of Cigarette Smoke Exposure in Mice.

Vanderstocken G, Marrow J, Allwood M, Stampfli M, Simpson J Front Physiol. 2020; 11:501383.

PMID: 33192539 PMC: 7609783. DOI: 10.3389/fphys.2020.501383.


Applications of a novel radiotelemetry method for the measurement of intrathoracic pressures and physiological rhythms in freely behaving mice.

Foster A, Marrow J, Allwood M, Brunt K, Simpson J J Appl Physiol (1985). 2020; 129(4):992-1005.

PMID: 32881619 PMC: 7654688. DOI: 10.1152/japplphysiol.00673.2019.


Hemodynamic assessment of diastolic function for experimental models.

Ogilvie L, Edgett B, Huber J, Platt M, Eberl H, Lutchmedial S Am J Physiol Heart Circ Physiol. 2020; 318(5):H1139-H1158.

PMID: 32216614 PMC: 7472516. DOI: 10.1152/ajpheart.00705.2019.


References
1.
Steiner A, Branco L . Hypoxia-induced anapyrexia: implications and putative mediators. Annu Rev Physiol. 2002; 64:263-88. DOI: 10.1146/annurev.physiol.64.081501.155856. View

2.
Stroka D, Burkhardt T, Desbaillets I, Wenger R, Neil D, Bauer C . HIF-1 is expressed in normoxic tissue and displays an organ-specific regulation under systemic hypoxia. FASEB J. 2001; 15(13):2445-53. DOI: 10.1096/fj.01-0125com. View

3.
Kim M, Platt M, Shibasaki T, Quaggin S, Backx P, Seino S . GLP-1 receptor activation and Epac2 link atrial natriuretic peptide secretion to control of blood pressure. Nat Med. 2013; 19(5):567-75. DOI: 10.1038/nm.3128. View

4.
Sheedy W, Thompson J, Morice A . A comparison of pathophysiological changes during hypobaric and normobaric hypoxia in rats. Respiration. 1996; 63(4):217-22. DOI: 10.1159/000196548. View

5.
Gonzalez N, Allen J, Schmidt E, Casillan A, Orth T, Wood J . Role of the renin-angiotensin system in the systemic microvascular inflammation of alveolar hypoxia. Am J Physiol Heart Circ Physiol. 2007; 292(5):H2285-94. DOI: 10.1152/ajpheart.00981.2006. View