Effect of Tiotropium Bromide on Airway Inflammation and Programmed Cell Death 5 in a Mouse Model of Ovalbumin-Induced Allergic Asthma

噻托溴铵对卵清蛋白诱发的过敏性哮喘小鼠模型中气道炎症和程序性细胞死亡 5 的影响

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作者:Juan Wang, Xiaolin Diao, Hong Zhu, Bei He

Conclusions

Tiotropium treatment may alleviate the pathological changes with asthma by regulating apoptosis.

Methods

We divided 12 female mice into 2 groups: untreated asthma (n = 6) and tiotropium-treated asthma (n = 6). The impact of tiotropium was assessed by histology of lung tissue and morphometry. Pulmonary function was tested by using pressure sensors. The number of cells in bronchoalveolar lavage fluid (BALF) was detected. Levels of PDCD5, active caspase-3, and muscarinic acetylcholine receptors M2 (ChRM2) and M3 (ChRM3) were examined.

Objective

To explore the role of tiotropium and its effect on PDCD5 level in a mouse model of chronic asthma.

Results

Tiotropium treatment significantly reduced airway inflammation and remodeling in asthmatic mice and intensified the lung function. PDCD5 level was reduced with tiotropium (p < 0.05). Moreover, active caspase-3 level was decreased with tiotropium (p < 0.001), and ChRM3 level was increased. Conclusions: Tiotropium treatment may alleviate the pathological changes with asthma by regulating apoptosis.

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