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氟替卡松/沙美特罗可减少严重马气喘的重塑和中性粒细胞炎症。

Fluticasone/salmeterol reduces remodelling and neutrophilic inflammation in severe equine asthma.

机构信息

Université de Montréal, Faculty of Veterinary Medicine, Department of Clinical Sciences, 3200 rue Sicotte, St-Hyacinthe, J2S 2M2, Quebec, Canada.

University of Edinburgh, Royal (Dick) School of Veterinary Studies, Easter Bush Campus, EH25 9RG, United Kingdom.

出版信息

Sci Rep. 2017 Aug 18;7(1):8843. doi: 10.1038/s41598-017-09414-8.

Abstract

Asthmatic airways are inflamed and undergo remodelling. Inhaled corticosteroids and long-acting β2-agonist combinations are more effective than inhaled corticosteroid monotherapy in controlling disease exacerbations, but their effect on airway remodelling and inflammation remains ill-defined. This study evaluates the contribution of inhaled fluticasone and salmeterol, alone or combined, to the reversal of bronchial remodelling and inflammation. Severely asthmatic horses (6 horses/group) were treated with fluticasone, salmeterol, fluticasone/salmeterol, or with antigen avoidance for 12 weeks. Lung function, central and peripheral airway remodelling, and bronchoalveolar inflammation were assessed. Fluticasone/salmeterol and fluticasone monotherapy decreased peripheral airway smooth muscle remodelling after 12 weeks (p = 0.007 and p = 0.02, respectively). On average, a 30% decrease was observed with both treatments. In central airways, fluticasone/salmeterol reversed extracellular matrix remodelling after 12 weeks, both within the lamina propria (decreased thickness, p = 0.005) and within the smooth muscle layer (p = 0.004). Only fluticasone/salmeterol decreased bronchoalveolar neutrophilia (p = 0.03) to the same extent as antigen avoidance already after 8 weeks. In conclusion, this study shows that fluticasone/salmeterol combination decreases extracellular matrix remodelling in central airways and intraluminal neutrophilia. Fluticasone/salmeterol and fluticasone monotherapy equally reverse peripheral airway smooth muscle remodelling.

摘要

哮喘气道会发生炎症和重塑。与吸入性皮质类固醇单药治疗相比,吸入皮质类固醇和长效β2-激动剂联合治疗更能有效控制疾病恶化,但它们对气道重塑和炎症的影响仍不明确。本研究评估了单独使用或联合使用吸入性氟替卡松和沙美特罗对逆转支气管重塑和炎症的作用。6 匹严重哮喘马(每组 6 匹)接受氟替卡松、沙美特罗、氟替卡松/沙美特罗或抗原回避治疗 12 周。评估肺功能、中央和外周气道重塑以及支气管肺泡炎症。氟替卡松/沙美特罗和氟替卡松单药治疗 12 周后均可减少外周气道平滑肌重塑(p=0.007 和 p=0.02)。平均而言,两种治疗方法均可使气道平滑肌减少 30%。在中央气道中,氟替卡松/沙美特罗在 12 周时逆转了细胞外基质重塑,无论是在固有层内(厚度减少,p=0.005)还是在平滑肌层内(p=0.004)。仅氟替卡松/沙美特罗在 8 周后即可使支气管肺泡嗜中性粒细胞减少(p=0.03),与抗原回避的效果相同。总之,本研究表明,氟替卡松/沙美特罗联合治疗可减少中央气道中的细胞外基质重塑和管腔内嗜中性粒细胞。氟替卡松/沙美特罗和氟替卡松单药治疗同样可逆转外周气道平滑肌重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b5b/5562887/aef2d4065045/41598_2017_9414_Fig1_HTML.jpg

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