Farré Núria, Otero Jorge, Falcones Bryan, Torres Marta, Jorba Ignasi, Gozal David, Almendros Isaac, Farré Ramon, Navajas Daniel
Heart Failure Unit, Department of Cardiology, Hospital del Mar, Barcelona, Spain.
Heart Diseases Biomedical Research Group, IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
Front Physiol. 2018 Aug 15;9:1143. doi: 10.3389/fphys.2018.01143. eCollection 2018.
Tissue hypoxia-reoxygenation characterizes obstructive sleep apnea (OSA), a very prevalent respiratory disease associated with increased cardiovascular morbidity and mortality. Experimental studies indicate that intermittent hypoxia (IH) mimicking OSA induces oxidative stress and inflammation in heart tissue at the cell and molecular levels. However, it remains unclear whether IH modifies the passive stiffness of the cardiac tissue extracellular matrix (ECM). To investigate multiscale changes of stiffness induced by chronic IH in the ECM of left ventricular (LV) myocardium in a murine model of OSA. Two-month and 18-month old mice ( = 10 each) were subjected to IH (20% O 40 s-6% O 20 s) for 6 weeks (6 h/day). Corresponding control groups for each age were kept under normoxia. Fresh LV myocardial strips (∼7 mm × 1 mm × 1 mm) were prepared, and their ECM was obtained by decellularization. Myocardium ECM macroscale mechanics were measured by performing uniaxial stress-strain tensile tests. Strip macroscale stiffness was assessed as the stress value (σ) measured at 0.2 strain and Young's modulus () computed at 0.2 strain by fitting Fung's constitutive model to the stress-strain relationship. ECM stiffness was characterized at the microscale as the Young's modulus () measured in decellularized tissue slices (∼12 μm tick) by atomic force microscopy. Intermittent hypoxia induced a ∼1.5-fold increase in σ ( < 0.001) and a ∼2.5-fold increase in ( < 0.001) of young mice as compared with normoxic controls. In contrast, no significant differences emerged in among IH-exposed and normoxic mice. Moreover, the mechanical effects of IH on myocardial ECM were similar in young and aged mice. The marked IH-induced increases in macroscale stiffness of LV myocardium ECM suggests that the ECM plays a role in the cardiac dysfunction induced by OSA. Furthermore, absence of any significant effects of IH on the microscale ECM stiffness suggests that the significant increases in macroscale stiffening are primarily mediated by 3D structural ECM remodeling.
组织缺氧-复氧是阻塞性睡眠呼吸暂停(OSA)的特征,OSA是一种非常普遍的呼吸系统疾病,与心血管发病率和死亡率增加相关。实验研究表明,模拟OSA的间歇性缺氧(IH)在细胞和分子水平上诱导心脏组织中的氧化应激和炎症。然而,尚不清楚IH是否会改变心脏组织细胞外基质(ECM)的被动僵硬度。为了研究在OSA小鼠模型中慢性IH诱导的左心室(LV)心肌ECM僵硬度的多尺度变化。将2个月和18个月大的小鼠(每组n = 10)进行6周(每天6小时)的IH(20% O₂ 40秒-6% O₂ 20秒)。每个年龄组的相应对照组保持在常氧条件下。制备新鲜的LV心肌条(约7毫米×1毫米×1毫米),并通过脱细胞获得其ECM。通过进行单轴应力-应变拉伸试验来测量心肌ECM的宏观力学。将条带的宏观僵硬度评估为在0.2应变时测量的应力值(σ),并通过将冯氏本构模型拟合到应力-应变关系来计算在0.2应变时的杨氏模量(E)。ECM僵硬度在微观尺度上表征为通过原子力显微镜在脱细胞组织切片(约12μm厚)中测量的杨氏模量(E)。与常氧对照组相比,间歇性缺氧使年轻小鼠的σ增加约1.5倍(P < 0.001),E增加约2.5倍(P < 0.001)。相比之下,暴露于IH的小鼠和常氧小鼠之间的E没有显著差异。此外,IH对年轻和老年小鼠心肌ECM的力学影响相似。IH诱导的LV心肌ECM宏观僵硬度的显著增加表明ECM在OSA诱导的心脏功能障碍中起作用。此外,IH对微观尺度ECM僵硬度没有任何显著影响,这表明宏观僵硬度的显著增加主要由3D结构ECM重塑介导。