McDonald Fiona B, Dempsey Eugene M, O'Halloran Ken D
Health Sciences Centre, 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 Mar 4;7:69. doi: 10.3389/fphys.2016.00069. eCollection 2016.
Intermittent hypoxia is a feature of apnea of prematurity (AOP), chronic lung disease, and sleep apnea. Despite the clinical relevance, the long-term effects of hypoxic exposure in early life on respiratory control are not well defined. We recently reported that exposure to chronic intermittent hypoxia (CIH) during postnatal development (pCIH) causes upper airway muscle weakness in both sexes, which persists for several weeks. We sought to examine if there are persistent sex-dependent effects of pCIH on respiratory muscle function into adulthood and/or increased susceptibility to re-exposure to CIH in adulthood in animals previously exposed to CIH during postnatal development. We hypothesized that pCIH would cause long-lasting muscle impairment and increased susceptibility to subsequent hypoxia. Within 24 h of delivery, pups and their respective dams were exposed to CIH: 90 s of hypoxia reaching 5% O2 at nadir; once every 5 min, 8 h per day for 3 weeks. Sham groups were exposed to normoxia in parallel. Three groups were studied: sham; pCIH; and pCIH combined with adult CIH (p+aCIH), where a subset of the pCIH-exposed pups were re-exposed to the same CIH paradigm beginning at 13 weeks. Following gas exposures, sternohyoid and diaphragm muscle isometric contractile and endurance properties were examined ex vivo. There was no apparent lasting effect of pCIH on respiratory muscle function in adults. However, in both males and females, re-exposure to CIH in adulthood in pCIH-exposed animals caused sternohyoid (but not diaphragm) weakness. Exposure to this paradigm of CIH in adulthood alone had no effect on muscle function. Persistent susceptibility in pCIH-exposed airway dilator muscle to subsequent hypoxic insult may have implications for the control of airway patency in adult humans exposed to intermittent hypoxic stress during early life.
间歇性缺氧是早产儿呼吸暂停(AOP)、慢性肺病和睡眠呼吸暂停的一个特征。尽管具有临床相关性,但早期生活中缺氧暴露对呼吸控制的长期影响尚不明确。我们最近报道,出生后发育期间暴露于慢性间歇性缺氧(CIH)(pCIH)会导致两性上呼吸道肌肉无力,这种情况会持续数周。我们试图研究pCIH对成年期呼吸肌功能是否存在持续性的性别依赖性影响,以及/或者在出生后发育期间暴露于CIH的动物成年后再次暴露于CIH时是否更易受影响。我们假设pCIH会导致长期的肌肉损伤,并增加对随后缺氧的易感性。在分娩后24小时内,幼崽及其各自的母鼠暴露于CIH:缺氧90秒,最低点时氧气浓度达到5%;每5分钟一次,每天8小时,持续3周。假手术组同时暴露于常氧环境。研究了三组:假手术组;pCIH组;以及pCIH联合成年期CIH(p+aCIH)组(其中一部分暴露于pCIH的幼崽从13周开始再次暴露于相同的CIH模式)。气体暴露后,离体检查胸骨舌骨肌和膈肌的等长收缩和耐力特性。pCIH对成年动物的呼吸肌功能没有明显的持续影响。然而,在雄性和雌性中,如果在成年期将之前暴露于pCIH的动物再次暴露于CIH,会导致胸骨舌骨肌(而非膈肌)无力。成年期单独暴露于这种CIH模式对肌肉功能没有影响。之前暴露于pCIH的气道扩张肌对随后缺氧损伤的持续易感性,可能对早年暴露于间歇性低氧应激的成年人类气道通畅性控制有影响。