首页> 外文期刊>Disease models & mechanisms: DMM >Long-term nose-only cigarette smoke exposure induces emphysema and mild skeletal muscle dysfunction in mice
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Long-term nose-only cigarette smoke exposure induces emphysema and mild skeletal muscle dysfunction in mice

机译:长期仅鼻子抽烟会引起小鼠肺气肿和轻度骨骼肌功能障碍

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Mouse models of chronic obstructive pulmonary disease (COPD) focus on airway inflammation and lung histology, but their use has been hampered by the lack of pulmonary function data in their assessment. Systemic effects such as muscle dysfunction are also poorly modeled in emphysematous mice. We aimed to develop a cigarette-smoke-induced emphysema mouse model in which serial lung function and muscular dysfunction could be assessed, allowing the disease to be monitored more appropriately. C57Bl6 mice were nose-only exposed to cigarette smoke or filtered air for 3–6 months. Lung function tests were repeated in the same mice after 3 and 6 months of cigarette smoke or air exposure and compared with lung histological changes. Contractile properties of skeletal muscles and muscle histology were also determined at similar time points in separate groups of mice. Serial lung function measurements documented hyperinflation after 3 and 6 months of cigarette smoke exposure, with a significant 31–37% increase in total lung capacity (TLC) and a significant 26–35% increase in compliance (Cchord) when compared with animals exposed to filtered air only ( P 0.001 after 3 and after 6 months). These functional changes preceded the changes in mean linear intercept, which became only significant after 6 months of cigarette smoke exposure and which correlated very well with TLC ( r =0.74, P =0.004) and Cchord ( r =0.79, P =0.001). After 6 months of cigarette smoke exposure, a significant fiber-type shift from IIa to IIx/b was also observed in the soleus muscle ( P 0.05), whereas a 20% reduction of force was present at high stimulation frequencies (80 Hz; P =0.09). The extensor digitorum longus (EDL) muscle was not affected by cigarette smoke exposure. These serial pulmonary function variables are sensitive outcomes to detect emphysema progression in a nose-only cigarette-smoke-exposed animal model of COPD. In this model, muscular changes became apparent only after 6 months, particularly in muscles with a mixed fiber-type composition.
机译:慢性阻塞性肺疾病(COPD)的小鼠模型侧重于气道炎症和肺组织学,但由于评估中缺少肺功能数据而受到阻碍。在气肿性小鼠中,诸如肌肉功能障碍之类的全身效应也很难建模。我们旨在开发一种香烟烟雾诱发的肺气肿小鼠模型,在该模型中可以评估一系列的肺功能和肌肉功能障碍,从而可以更适当地监测疾病。 C57Bl6小鼠仅鼻子接触香烟烟雾或过滤空气3-6个月。在吸烟和接触空气3个月和6个月后,在同一只小鼠中重复进行肺功能测试,并将其与肺组织学变化进行比较。在相似的时间点,在单独的小鼠组中还确定了骨骼肌的收缩特性和肌肉组织学。连续的肺功能测量结果表明,接触香烟的3个月和6个月后恶性通气,与暴露于动物的动物相比,总肺活量(TLC)显着增加31–37%,顺应性(Cchord)显着增加26–35%仅过滤空气(3个月后和6个月后P <0.001)。这些功能性变化发生在平均线性截距变化之前,平均线性截距变化仅在接触香烟烟雾六个月后才变得显着,并且与TLC(r = 0.74,P = 0.004)和Cchord(r = 0.79,P = 0.001)密切相关。接触香烟烟雾6个月后,在比目鱼肌中也观察到了从IIa到IIx / b的明显纤维类型转变(P <0.05),而在高刺激频率(80 Hz; 80 Hz; 20 Hz)下力量降低了20%。 P = 0.09)。指伸伸肌(EDL)肌肉不受香烟烟雾暴露的影响。这些连续的肺功能变量是敏感的结果,可用于在仅鼻烟暴露的COPD动物模型中检测肺气肿的进展。在该模型中,肌肉变化仅在6个月后才变得明显,特别是在混合纤维类型成分的肌肉中。

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