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持续性低氧对发育过程中胸骨舌骨肌和膈肌的影响。

Effects of sustained hypoxia on sternohyoid and diaphragm muscle during development.

机构信息

University College Dublin, Dublin.

出版信息

Eur Respir J. 2014 Apr;43(4):1149-58. doi: 10.1183/09031936.00139512. Epub 2013 Jun 13.

Abstract

Sustained hypoxia is a dominant feature of respiratory disease. Despite the clinical significance, the effects of sustained hypoxia on the form and function of respiratory muscle during development are relatively underexplored. Wistar rats were exposed to 1 week of sustained hypoxia (ambient pressure 450 mmHg) or normoxia at various time points during development. Sternohyoid and diaphragm muscle contractile and endurance properties were assessed in vitro. Muscle succinate dehydrogenase and myosin heavy chain composition were determined. The role of reactive oxygen species in hypoxia-induced muscle remodelling was assessed. Sustained hypoxia increased sternohyoid muscle force and fatigue in early but not late development, effects that persisted after return to normoxia. Hypoxia-induced sternohyoid muscle fatigue was not attributable to fibre type transitions or to a decrease in oxidative capacity. Chronic supplementation with the superoxide scavenger tempol did not prevent hypoxia-induced sternohyoid muscle fatigue, suggesting that mechanisms unrelated to oxidative stress underpin hypoxia-induced maladaptation in sternohyoid muscle. Sustained hypoxia had no effect on diaphragm muscle fatigue. We conclude that there are critical windows during development for hypoxia-induced airway dilator muscle maladaptation. Sustained hypoxia-induced impairment of upper airway muscle endurance may persist into later life. Upper airway muscle dysfunction could have deleterious consequences for the control of pharyngeal airway calibre in vivo.

摘要

持续缺氧是呼吸疾病的主要特征。尽管具有临床意义,但持续缺氧对呼吸肌在发育过程中的形态和功能的影响仍未得到充分探索。将 Wistar 大鼠在发育过程中的不同时间点暴露于持续缺氧(环境压力 450mmHg)或常氧中 1 周。在体外评估胸锁乳突肌和膈肌的收缩和耐力特性。测定肌肉琥珀酸脱氢酶和肌球蛋白重链组成。评估活性氧在缺氧诱导的肌肉重塑中的作用。持续缺氧增加了早期但不是晚期发育中的胸锁乳突肌力量和疲劳,这些影响在返回常氧后仍然存在。缺氧诱导的胸锁乳突肌疲劳不是由于纤维类型转变或氧化能力下降引起的。慢性补充超氧化物清除剂 tempol 不能预防缺氧诱导的胸锁乳突肌疲劳,这表明缺氧诱导的胸锁乳突肌适应不良的机制与氧化应激无关。持续缺氧对膈肌疲劳没有影响。我们得出结论,在发育过程中有特定的关键时期会导致气道扩张肌的缺氧适应不良。持续缺氧引起的上气道肌肉耐力损伤可能会持续到以后的生活。上气道肌肉功能障碍可能对体内咽气道口径的控制产生有害影响。

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