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Effect of aging on airway remodeling and muscarinic receptors in a murine acute asthma model

机译:衰老对小鼠急性哮喘模型气道重塑和毒蕈碱受体的影响

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Background and objectives: The influence of aging on the development of asthma has not been studied thoroughly. The aim of this study was to investigate age-related airway responses involving lung histology and expression of muscarinic receptors in a murine model of acute asthma. Methods: Female BALB/c mice at the ages of 6 weeks and 6, 9, and 12 months were sensitized and challenged with ovalbumin (OVA) for 1 month (n = 8–12 per group). We analyzed inflammatory cells and T-helper (Th)2 cytokines in bronchoalveolar lavage (BAL) fluid and parameters of airway remodeling and expression of muscarinic receptors in lung tissue. Results: Among the OVA groups, total cell and eosinophil numbers in BAL fluid were significantly higher in the older (6-, 9-, and 12-month-old) mice than in the young (6-week-old) mice. Interleukin (IL) 4 (IL-4) concentration increased, but IL-5 and IL-13 concentrations showed a decreased tendency, with age. IL-17 concentration tended to increase with age, which did not reach statistical significance. periodic acid-Schiff (PAS) staining area, peribronchial collagen deposition, and area of α-smooth muscle staining were significantly higher in the 6-month older OVA group than in the young OVA group. The expression of the M3 and M2 muscarinic receptors tended to increase and decrease, respectively, with age. Conclusion: The aged mice showed an active and unique pattern not only on airway inflammation, but also on airway remodeling and expression of the muscarinic receptors during the development of acute asthma compared with the young mice. These findings suggest that the aging process affects the pathogenesis of acute asthma and age-specific approach might be more appropriate for better asthma control in a clinical practice.
机译:背景与目的:衰老对哮喘发展的影响尚未得到充分研究。这项研究的目的是调查急性哮喘小鼠模型中涉及肺组织学和毒蕈碱受体表达的年龄相关气道反应。方法:对6周龄,6、9、9和12个月大的BALB / c雌性小鼠进行敏化并用卵清蛋白(OVA)攻击1个月(每组n = 8–12)。我们分析了支气管肺泡灌洗(BAL)液中的炎症细胞和T辅助(Th)2细胞因子,以及肺组织中气道重塑和毒蕈碱受体表达的参数。结果:在OVA组中,老年(6、9和12个月大)小鼠的BAL液中的总细胞和嗜酸性粒细胞数量显着高于年轻(6周龄)的小鼠。白介素(IL)4(IL-4)浓度增加,但IL-5和IL-13浓度随年龄增长而降低。 IL-17浓度随年龄增长而增加,但没有统计学意义。 6个月大的OVA组中高碘酸-希夫(PAS)染色面积,支气管周胶原沉积和α平滑肌染色面积显着高于年轻的OVA组。 M3和M2毒蕈碱受体的表达会随着年龄的增长而分别增加和减少。结论:与年轻小鼠相比,衰老小鼠在急性哮喘发展过程中不仅在气道炎症,而且在气道重塑和毒蕈碱受体表达上都表现出活跃而独特的模式。这些发现表明,衰老过程会影响急性哮喘的发病机理,在临床实践中,针对年龄的方法可能更适合于更好地控制哮喘。

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