McDonald Fiona B, Dempsey Eugene M, O'Halloran Ken D
Department of Physiology, School of Medicine and Medical Science, University College Dublin Dublin, Ireland.
Department of Paediatrics and Child Health, Cork University Maternity Hospital and the Irish Centre for Fetal and Neonatal Translational Research, University College Cork Cork, Ireland.
Front Physiol. 2016 Jul 12;7:276. doi: 10.3389/fphys.2016.00276. eCollection 2016.
Alterations to the supply of oxygen during early life presents a profound stressor to physiological systems with aberrant remodeling that is often long-lasting. Chronic intermittent hypoxia (CIH) is a feature of apnea of prematurity, chronic lung disease, and sleep apnea. CIH affects respiratory control but there is a dearth of information concerning the effects of CIH on respiratory muscles, including the diaphragm-the major pump muscle of breathing. We investigated the effects of exposure to gestational CIH (gCIH) and postnatal CIH (pCIH) on diaphragm muscle function in male and female rats. CIH consisted of exposure in environmental chambers to 90 s of hypoxia reaching 5% O2 at nadir, once every 5 min, 8 h a day. Exposure to gCIH started within 24 h of identification of a copulation plug and continued until day 20 of gestation; animals were studied on postnatal day 22 or 42. For pCIH, pups were born in normoxia and within 24 h of delivery were exposed with dams to CIH for 3 weeks; animals were studied on postnatal day 22 or 42. Sham groups were exposed to normoxia in parallel. Following gas exposures, diaphragm muscle contractile, and endurance properties were examined ex vivo. Neither gCIH nor pCIH exposure had effects on diaphragm muscle force-generating capacity or endurance in either sex. Similarly, early life exposure to CIH did not affect muscle tolerance of severe hypoxic stress determined ex vivo. The findings contrast with our recent observation of upper airway dilator muscle weakness following exposure to pCIH. Thus, the present study suggests a relative resilience to hypoxic stress in diaphragm muscle. Co-ordinated activity of thoracic pump and upper airway dilator muscles is required for optimal control of upper airway caliber. A mismatch in the force-generating capacity of the complementary muscle groups could have adverse consequences for the control of airway patency and respiratory homeostasis.
生命早期氧气供应的改变对生理系统是一个巨大的应激源,会导致异常重塑,且这种重塑往往持续时间很长。慢性间歇性缺氧(CIH)是早产儿呼吸暂停、慢性肺病和睡眠呼吸暂停的一个特征。CIH会影响呼吸控制,但关于CIH对呼吸肌(包括呼吸的主要泵血肌——膈肌)影响的信息却很匮乏。我们研究了孕期暴露于CIH(gCIH)和出生后暴露于CIH(pCIH)对雄性和雌性大鼠膈肌功能的影响。CIH包括每天8小时在环境舱中暴露于低氧环境,每隔5分钟出现一次,最低氧含量达到5% O₂,持续90秒。暴露于gCIH在确认交配栓后的24小时内开始,并持续到妊娠第20天;在出生后第22天或第42天对动物进行研究。对于pCIH,幼崽在常氧环境中出生,出生后24小时内与母鼠一起暴露于CIH环境中3周;在出生后第22天或第42天对动物进行研究。假手术组则同时暴露于常氧环境。气体暴露后,离体检测膈肌的收缩和耐力特性。gCIH和pCIH暴露对两性的膈肌力量产生能力或耐力均无影响。同样,生命早期暴露于CIH也不影响离体测定的对严重低氧应激的肌肉耐受性。这些发现与我们最近观察到的暴露于pCIH后上气道扩张肌无力的结果形成对比。因此,本研究表明膈肌对低氧应激具有相对的恢复力。胸廓泵血肌和上气道扩张肌的协调活动对于上气道口径的最佳控制是必需的。互补肌群力量产生能力的不匹配可能会对气道通畅性和呼吸稳态的控制产生不利影响。