| Literature DB >> 25962375 |
Ricardo Costa Petroni1,2, Paolo Jose Cesare Biselli3, Thais Martins de Lima3, Mariana Cardillo Theobaldo3, Elia Tamaso Caldini4, Rosângela Nascimento Pimentel3, Hermes Vieira Barbeiro3, Suely Ariga Kubo3, Irineu Tadeu Velasco3, Francisco Garcia Soriano3.
Abstract
Acute respiratory distress syndrome (ARDS) is the most severe lung inflammatory manifestation and has no effective therapy nowadays. Sepsis is one of the main illnesses among ARDS causes. The use of fluid resuscitation is an important treatment for sepsis, but positive fluid balance may induce pulmonary injury. As an alternative, fluid resuscitation with hypertonic saline ((HS) NaCl 7.5%) has been described as a promising therapeutical agent in sepsis-induced ARDS by the diminished amount of fluid necessary. Thus, we evaluated the effect of hypertonic saline in the treatment of LPS-induced ARDS. We found that hypertonic saline (NaCl 7.5%) treatment in rat model of LPS-induced ARDS avoided pulmonary function worsening and inhibited type I collagen deposition. In addition, hypertonic saline prevented pulmonary injury by decreasing metalloproteinase 9 (MMP-9) activity in tissue. Focal adhesion kinase (FAK) activation was reduced in HS group as well as neutrophil infiltration, NOS2 expression and NO content. Our study shows that fluid resuscitation with hypertonic saline decreases the progression of LPS-induced ARDS due to inhibition of pulmonary remodeling that is observed when regular saline is used.Entities:
Keywords: acute lung injury; fluid resuscitation; focal adhesion kinase; nitric oxide; pulmonary fibrosis
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Year: 2015 PMID: 25962375 DOI: 10.1007/s10753-015-0183-4
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092