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N-乙酰半胱氨酸对气道黏液高分泌的影响:系统评价。

Impact of N-Acetylcysteine on Mucus Hypersecretion in the Airways: A Systematic Review.

机构信息

Unit of Respiratory Medicine, Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.

Respiratory Disease and Lung Function Unit, Department of Medicine and Surgery, University of Parma, Parma, Italy.

出版信息

Int J Chron Obstruct Pulmon Dis. 2024 Oct 29;19:2347-2360. doi: 10.2147/COPD.S474512. eCollection 2024.

Abstract

Mucus clearance is crucial for airway protection, and its dysfunction leads to chronic obstructive pulmonary disease (COPD) characterized by mucus hypersecretion (MHS) and impaired clearance. MUC5AC and MUC5B mucin proteins are key components of airway mucus, with MUC5AC being particularly responsive to environmental stimuli, making it a potential COPD biomarker. N-acetylcysteine (NAC) is a mucolytic agent with known effects on mucus viscosity and clearance, but its precise mechanisms in COPD remain unclear. This systematic review evaluated the impact of NAC on MHS in the airways, reporting significant inhibitory effects on MUC5AC and MUC5B gene and protein expression, as well as a reduction in the number of goblet cells. NAC has demonstrated efficacy in vitro and in animal models of MHS, including COPD models, but data on human bronchial tissue are lacking. This systematic review suggests that NAC acts as a mucolytic and a mucoregulator, directly inhibiting mucus secretion and goblet cell hyperplasia. Given the critical role of MHS in COPD progression, exacerbations, and mortality, these findings highlight the potential of NAC as a targeted therapy for hypersecretion COPD phenotypes. However, further studies are needed to confirm the results of this systematic review, even in human bronchial tissue, to provide translatable evidence in clinical settings. Understanding the intimate mechanism of NAC MHS regulation may pave the way for more effective treatments targeting airway mucus dysfunction in COPD, ultimately improving patient outcomes and reducing morbidity and mortality associated with chronic mucus hypersecretion.

摘要

黏液清除对于气道保护至关重要,其功能障碍导致慢性阻塞性肺疾病(COPD),其特征为黏液高分泌(MHS)和清除受损。黏蛋白 MUC5AC 和 MUC5B 是气道黏液的关键成分,其中 MUC5AC 对环境刺激特别敏感,使其成为潜在的 COPD 生物标志物。N-乙酰半胱氨酸(NAC)是一种黏液溶解剂,已知对黏液粘度和清除有影响,但在 COPD 中的确切机制尚不清楚。本系统评价评估了 NAC 对气道 MHS 的影响,报告称其对 MUC5AC 和 MUC5B 基因和蛋白表达具有显著抑制作用,并减少了杯状细胞的数量。NAC 已在体外和 MHS 的动物模型中显示出疗效,包括 COPD 模型,但缺乏人类支气管组织的数据。本系统评价表明,NAC 作为黏液溶解剂和黏液调节剂发挥作用,直接抑制黏液分泌和杯状细胞增生。鉴于 MHS 在 COPD 进展、加重和死亡率中的关键作用,这些发现强调了 NAC 作为针对高分泌 COPD 表型的靶向治疗的潜力。然而,需要进一步的研究来证实本系统评价的结果,即使在人类支气管组织中也是如此,以在临床环境中提供可转化的证据。了解 NAC 调节 MHS 的内在机制可能为靶向治疗 COPD 气道黏液功能障碍铺平道路,最终改善患者结局并降低与慢性黏液高分泌相关的发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3d7/11531296/4d0d16ef677c/COPD-19-2347-g0001.jpg

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