ea0056gp67 | Cardiovascular | ECE2018
Gomez Juan Fandino
, Estevez Laura Toba
, Vaz Ana Alvarez
, Matias Lucas Carmelo Gonzalez
, Chaves Yolanda Diz
, Ferrer Federico Mallo
Idiopathic pulmonary fibrosis (IPF) is an excessive accumulation of fibrous filaments in the extracellular matrix (ECM), in response to an inflammatory reaction that disrupts normal lung architecture and physiology. Collagen is the most abundant fibrous protein in the ECM. The GLP-1 receptor is highly expressed on lung tissue, where his activation plays an essential role in the synthesis and secretion of surfactant proteins. The objective of this study was to elucidate the eff...