Allium sativum nanovesicles exhibit anti-inflammatory and antifibrotic activity in a bleomycin-induced lung fibrosis model

Background Idiopathic pulmonary fibrosis (IPF) is a chronic and highly fatal disease characterized by excessive accumulation of extracellular matrix (ECM), foci of myofibroblasts, and a usual pattern of interstitial pneumonia. As suggested by international guidelines, the treatment for this disease...

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Veröffentlicht in:Molecular biology reports 2024-12, Vol.51 (1), p.1166, Article 1166
Hauptverfasser: Santos-Álvarez, Jovito Cesar, Velázquez-Enríquez, Juan Manuel, Reyes-Jiménez, Edilburga, Ramírez-Hernández, Alma Aurora, Iñiguez-Palomares, Ramon, Rodríguez-Beas, César, Canseco, Socorro Pina, Aguilar-Ruiz, Sergio Roberto, Castro-Sánchez, Luis, Vásquez-Garzón, Verónica Rocío, Baltiérrez-Hoyos, Rafael
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Sprache:eng
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Zusammenfassung:Background Idiopathic pulmonary fibrosis (IPF) is a chronic and highly fatal disease characterized by excessive accumulation of extracellular matrix (ECM), foci of myofibroblasts, and a usual pattern of interstitial pneumonia. As suggested by international guidelines, the treatment for this disease involves supportive therapies, as there is currently no effective treatment. Plant-derived nanovesicles have emerged as a new treatment for various diseases and have been tested in cellular and murine models. Methods and results This research aimed to test the use of Allium sativum nanovesicles (AS-NV) in a murine model of IPF induced by bleomycin. AS-NV reduced the amount of collagen and restored lung architecture in the mouse model. AS-NV was tested on human lung fibroblasts, which do not affect the viability of healthy cells. AS-NV treatment decreases the mRNA levels of genes related to fibrosis, inflammation, and ECM deposition ( Mmp2 , Timp-2 , Vegf , Pcna , Col1a1 , Tgf-β , α-Sma , IL-1β , and Hif1a ) in bleomycin-induced idiopathic pulmonary fibrosis. Conclusions This research highlights the anti-inflammatory and antifibrotic activity of AS-NV, which contributes to plant nanovesicle mechanisms in IPF; however, more AS-NV studies are needed to identify alternative treatments for idiopathic pulmonary fibrosis.
ISSN:0301-4851
1573-4978
1573-4978
DOI:10.1007/s11033-024-10104-8