Does sleep apnea exacerbate respiratory muscle dysfunction in muscular dystrophy?

睡眠呼吸暂停是否会加剧肌营养不良症患者的呼吸肌功能障碍？

• 批准号: 7531249
• 负责人: GASPAR Andrew FARKAS
• 金额: $ 20.92万
• 依托单位: STATE UNIVERSITY OF NEW YORK AT BUFFALO
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-02 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7531249
• 关键词: Acetylcysteine; Address; Animal Model; Attenuated; Biochemical; Biochemical Markers; Breathing; Cause of Death; Cell physiology; Cells; Collagen; Condition; Data; Diagnosis; Disease; Duchenne muscular dystrophy; Dystrophin; Elevation; Environmental air flow; Event; Exposure to; Failure; Fiber; Fibrosis; Functional disorder; Gases; Histologic; Hypoxia; Inflammation; Inflammatory; Injury; Ischemia; Lead; Link; Lipid Peroxidation; Lung; Measures; Mechanical Stress; Mechanics; Mediating; Mediator of activation protein; Membrane; Modality; Mus; Muscle; Muscle Cells; Muscle function; Muscular Dystrophies; Mutation; Myosin Heavy Chains; Nature; Neuromuscular Diseases; Organ failure; Output; Oxidative Stress; Oxygen; Oxygen measurement, partial pressure, arterial; Pathogenesis; Patients; Physiological; Production; Proteins; Public Health; Reactive Oxygen Species; Reporting; Respiratory Diaphragm; Respiratory Muscles; Role; Seminal; Signal Transduction; Simulate; Sleep; Sleep Apnea Syndromes; Sleep Architecture; Stress; TNF gene; Testing; Toxic Actions; Urination; Week; cytokine; day; functional decline; infliximab; novel therapeutics; prevent; response; size; stressor; tadalafil

DESCRIPTION (provided by applicant): Duchenne muscular dystrophy (DMD), a fatal and crippling disease, results from a mutation of the membrane stabilizing protein dystrophin. Dystrophin-deficient muscles are more susceptible than normal to a variety of stresses. The respiratory muscles are critical for survival and their failure is a leading cause of death in DMD. Sleep disturbed breathing (SDB) is common and nocturnal gas exchange abnormalities and disrupted sleep architecture, hallmarks of SDB, have been reported in > 80% of DMD patients. Reduced ventilation during sleep results in cyclic decreases in arterial oxygen tensions (hypoxia), in elevations of several inflammatory cytokines including TNF-1, and in the production of reactive oxygen species (ROS), all of which can putatively impact muscle cell function. In addition, physiologic responses to cyclic alterations in oxygen levels that accompany SDB include increased sympathetic discharge and enhanced activation of the respiratory muscles (upper airway and ventilatory), factors which can also impact muscle function. Despite the pervasiveness of SDB in DMD patients, the effects of SDB on respiratory muscle function in DMD remain unknown. We hypothesize that SDB exacerbates dysfunction of the respiratory muscle in DMD. Preliminary data in dystrophic mice (Dmdmdx) reveal that experimental sleep apnea intensifies functional declines in diaphragm contractility. Proposed studies will delineate mechanical and biochemical mechanisms responsible for SDB induced respiratory muscle dysfunction in an animal model of DMD. More specifically, the proposed studies will assess 1) the putative impact of enhanced muscle recruitment (mechanical stress) in response to episodic hypoxia on respiratory muscle function; 2) to assess the putative role mediated by TNF-1 mechanisms; and 3) to assess the role attributed to oxidative stress in mediating SDB dysfunction of dystrophin-deficient respiratory muscles. To this end, SDB will be simulated in Dmdmdx- mice with long term (up to 12 weeks) diurnal (8 hrs per day, 5 days a week) exposure to experimental sleep apnea (episodic hypoxia). The dysfunction of the respiratory muscles will be assessed by measuring functional parameters (breathing strategies, force output and fatigability of isolated muscle bundles), biochemical markers (collagen content, lipid peroxidation, and inflammatory cytokines), and histological/ morphometric markers (central nucleation, fiber size, and extent of fiber loss and fibrosis). PUBLIC HEALTH RELEVANCE. Sleep disordered breathing (SDB) is prevalent in Duchenne Muscular Dystrophy (DMD) and may exacerbate dysfunction of the respiratory muscles. Studies will investigate several putative mechanisms (mechanical and biochemical stressors) that contribute to respiratory muscle dysfunction using Dmdmdx-mice. Since respiratory muscle failure is a leading cause of death in DMD, these studies will reveal new therapeutic modalities aimed at preventing respiratory muscle failure in DMD.

描述（由申请人提供）：杜氏肌营养不良症（DMD）是一种致命的致残性疾病，由膜稳定蛋白肌营养不良蛋白突变引起。肌营养不良蛋白缺乏的肌肉比正常的更容易受到各种压力的影响。呼吸肌对生存至关重要，其衰竭是DMD患者死亡的主要原因。睡眠呼吸障碍（SDB）很常见，夜间气体交换异常和睡眠结构紊乱是SDB的标志，据报道，80%的DMD患者存在睡眠呼吸障碍。睡眠时通气减少会导致动脉氧张力（缺氧）的周期性下降，包括TNF-1在内的几种炎症细胞因子的升高，以及活性氧（ROS）的产生，所有这些都可能影响肌肉细胞的功能。此外，伴随SDB的氧水平周期性变化的生理反应包括交感放电增加和呼吸肌（上呼吸道和通气）激活增强，这些因素也可以影响肌肉功能。尽管SDB在DMD患者中普遍存在，但SDB对DMD患者呼吸肌功能的影响尚不清楚。我们假设SDB加重了DMD患者的呼吸肌功能障碍。营养不良小鼠（Dmdmdx）的初步数据显示，实验性睡眠呼吸暂停加剧了膈肌收缩功能的下降。拟议的研究将在DMD动物模型中描述SDB诱导的呼吸肌功能障碍的机械和生化机制。更具体地说，拟议的研究将评估1)偶发性缺氧对呼吸肌功能的影响，即肌肉补充增强（机械应力）；2)评估TNF-1机制介导的可能作用；3)探讨氧化应激在肌营养不良蛋白缺乏的呼吸肌SDB功能障碍中的作用。为此，SDB将在长期（长达12周）每天（每天8小时，每周5天）暴露于实验性睡眠呼吸暂停（间歇性缺氧）的Dmdmdx小鼠中进行模拟。通过测量功能参数（呼吸策略、力输出和分离肌束的疲劳程度）、生化指标（胶原含量、脂质过氧化和炎性细胞因子）和组织学/形态计量指标（中心成核、纤维大小、纤维损失和纤维化程度）来评估呼吸肌功能障碍。公共卫生相关性。睡眠呼吸障碍（SDB）在杜氏肌营养不良症（DMD）中很普遍，并可能加剧呼吸肌功能障碍。研究将利用dmdmdx小鼠研究几种可能导致呼吸肌功能障碍的机制（机械和生化应激源）。由于呼吸肌肉衰竭是DMD的主要死亡原因，这些研究将揭示新的治疗方式，旨在预防DMD的呼吸肌肉衰竭。