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Differential effects of Nintedanib and Pirfenidone on lung alveolar epithelial cell function in ex vivo murine and human lung tissue cultures of pulmonary fibrosis.
Author: AlsafadiHani N, BehrJürgen, BuhlLara, HermannSarah, HilgendorffAnne, KleeStephan, KönigshoffMelanie, LehmannMareike, LindnerMichael, MutzeKathrin, OtaChiharu, WagnerDarcy E
Original Abstract of the Article :
Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease. Repetitive injury and reprogramming of the lung epithelium are thought to be critical drivers of disease progression, contributing to fibroblast activation, extracellular matrix remodeling, and subsequently loss of lung archit...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138909/
データ提供:米国国立医学図書館(NLM)
Nintedanib and Pirfenidone: Differential Effects on Lung Epithelial Cells in Pulmonary Fibrosis
The study of pulmonary fibrosis, a debilitating lung disease, is a challenging journey through a desert of unanswered questions. This research explores the effects of two approved drugs, nintedanib and pirfenidone, on lung alveolar epithelial cell function in ex vivo murine and human lung tissue cultures. The researchers found that both drugs have distinct effects on lung epithelial cell function. While both drugs are approved for treating pulmonary fibrosis, their mechanisms of action are distinct. This research provides valuable insights into the complex interplay between these drugs and the lung epithelium.
Nintedanib and Pirfenidone: Distinct Mechanisms in Pulmonary Fibrosis
The study highlights the distinct mechanisms of action of nintedanib and pirfenidone on lung epithelial cells. This finding suggests that these drugs might have different therapeutic effects and could be used in combination to optimize treatment outcomes.
Pulmonary Fibrosis: A Complex and Challenging Disorder
Pulmonary fibrosis is a complex and challenging disorder. The quest for effective treatments continues, with ongoing research exploring a wide range of potential therapies. This research provides valuable insights into the potential of targeting lung epithelial cell function as a strategy for treating this debilitating disease.
Dr.Camel's Conclusion
The desert of pulmonary fibrosis research is vast and demanding. This study sheds light on the complex interplay between two approved drugs, nintedanib and pirfenidone, and their differential effects on lung epithelial cells. This research highlights the need for continued research into new and effective therapies for this challenging disease.
Date :
- Date Completed 2018-12-11
- Date Revised 2018-12-11
Further Info :
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