Department of Human Health and Nutritional Sciences, University of Guelph, 50 Stone Road East, Guelph, ON, Canada.
Department of Pharmacology, Dalhousie Medicine New Brunswick, 100 Tucker Park Road, Saint John, New Brunswick, Canada.
J Physiol. 2018 Aug;596(15):3391-3410. doi: 10.1113/JP275945. Epub 2018 May 13.
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.
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.
在本研究中,我们提供了与严重程度、缺氧持续时间和后效相关的重要知识空白的证据,证明了中度与重度缺氧时人体会产生不同的生理反应。中度和重度缺氧的生理反应与时间既不成比例,也不是线性关系,更不是同时发生。中度缺氧会引起与严重程度相关的生理反应,这些反应在恢复到正常氧合时会持续存在或波动。这些不同的心血管反应的生理基础表明,自主神经系统的交感神经-迷走神经平衡点发生了转移,而不是由于缺氧应激导致动脉的分子变化。
缺氧既是许多急性和慢性疾病的结果,也是其原因。严重缺氧会导致高血压和心血管后遗症;然而,少数使用中度缺氧程度的研究表明,中度缺氧可能是有益的,这表明缺氧并不总是有害的。由于不同的缺氧严重程度分类、输送方法和麻醉剂的使用,研究之间的比较较为困难。因此,为了研究中度缺氧对心血管健康的长期影响,使用无线电遥测技术在未麻醉的小鼠中获得了 24 小时中度或重度缺氧以及随后 72 小时正常氧合恢复期间的体内生理测量。中度缺氧后的恢复期间,收缩压降低,但重度缺氧后则升高。中度和重度缺氧都增加了恢复期间动脉中血红素加氧酶-1 的表达,这表明在动脉水平上存在同等的缺氧应激。只有重度而非中度缺氧增加了心率变异性的低/高频比值,表明交感神经-迷走神经平衡发生了转移。中度缺氧抑制了昼夜节律的振幅,而重度缺氧则在整个缺氧过程中破坏了节律,并且在正常氧合恢复期间仍存在波动。因此,缺氧的严重程度会对昼夜节律血压产生不同的调节作用。