دورية أكاديمية

Combination Therapy With Polydeoxyribonucleotide and Pirfenidone Alleviates Symptoms of Acute Respiratory Distress Syndrome in Human Lung Epithelial A549 Cells

التفاصيل البيبلوغرافية
العنوان: Combination Therapy With Polydeoxyribonucleotide and Pirfenidone Alleviates Symptoms of Acute Respiratory Distress Syndrome in Human Lung Epithelial A549 Cells
المؤلفون: Jae-Joon Hwang, Il-Gyu Ko, Jun-Jang Jin, Lakkyong Hwang, Sang-Hoon Kim, Jung Won Jeon, Seung Sook Paik, Bok Soon Chang, Cheon Woong Choi
المصدر: International Neurourology Journal, Vol 24, Iss Suppl 1, Pp S56-64 (2020)
بيانات النشر: Korean Continence Society, 2020.
سنة النشر: 2020
المجموعة: LCC:Diseases of the genitourinary system. Urology
مصطلحات موضوعية: acute respiratory distress syndrome, polydeoxyribonucleotide, pirfenidone, combination therapy, Diseases of the genitourinary system. Urology, RC870-923
الوصف: Purpose Acute respiratory distress syndrome (ARDS) is characterized by its acute onset of symptoms such as bilateral pulmonary infiltrates, severe hypoxemia, and pulmonary edema. Many patients with ARDS survive in the acute phase, but then die from significant lung fibrosis. Methods The effect of combination therapy with polydeoxyribonucleotide (PDRN) and pirfenidone on ARDS was investigated using human lung epithelial A549 cells. ARDS environment was induced by treatment with lipopolysaccharide and transforming growth factor (TGF)-β. Enzyme-linked immunoassay for connective tissue growth factor (CTGF) and hydroxyproline were conducted. Western blot for collagen type I, fibroblast growth factor (FGF), tumor necrosis factor (TNF)-α, and interleukin (IL)-6 was performed. Results In this study, 8-μg/mL PDRN enhanced cell viability. Combination therapy with PDRN and pirfenidone and pirfenidone monotherapy suppressed expressions of CTGF and hydroxyproline and inhibited expressions of collagen type I and FGF. Combination therapy with PDRN and pirfenidone and PDRN monotherapy suppressed expression of TNF-α and IL-1β. Conclusions The combination therapy with PDRN and pirfenidone exerted stronger therapeutic effect against lipopolysaccharide and TGF-β-induced ARDS environment compared to the PDRN monotherapy or pirfenidone monotherapy. The excellent therapeutic effect of combination therapy with PDRN and pirfenidone on ARDS was shown by promoting the rapid anti-inflammatory effect and inhibiting the fibrotic processes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2093-4777
2093-6931
Relation: http://www.einj.org/upload/pdf/inj-2040152-076.pdf; https://doaj.org/toc/2093-4777; https://doaj.org/toc/2093-6931
DOI: 10.5213/inj.2040152.076
URL الوصول: https://doaj.org/article/b730ca266c8341c180b8092b4275f814
رقم الأكسشن: edsdoj.b730ca266c8341c180b8092b4275f814
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20934777
20936931
DOI:10.5213/inj.2040152.076