Emphysema induced by elastase enhances acute inflammatory pulmonary response to intraperitoneal LPS in rats.
Lídia Maria Carneiro da FonsecaMaycon Moura ReboredoLeda Marília Fonseca LucindaThaís Fernanda FazzaMaria Aparecida Esteves RabeloAdenilson Souza FonsecaFlavia de PaoliBruno Valle PinheiroPublished in: International journal of experimental pathology (2016)
Abnormalities in lungs caused by emphysema might alter their response to sepsis and the occurrence of acute lung injury (ALI). This study compared the extension of ALI in response to intraperitoneal lipopolysaccharide (LPS) injection in Wistar rats with and without emphysema induced by elastase. Adult male Wistar rats were randomized into four groups: control, emphysema without sepsis, normal lung with sepsis and emphysema with sepsis. Sepsis was induced, and 24 h later the rats were euthanised. The following analysis was performed: blood gas measurements, bronchoalveolar lavage (BAL), lung permeability and histology. Animals that received LPS showed significant increase in a lung injury scoring system, inflammatory cells in bronchoalveolar lavage (BAL) and IL-6, TNF-α and CXCL2 mRNA expression in lung tissue. Animals with emphysema and sepsis showed increased alveolocapillary membrane permeability, demonstrated by higher BAL/serum albumin ratio. In conclusion, the presence of emphysema induced by elastase increases the inflammatory response in the lungs to a systemic stimulus, represented in this model by the intraperitoneal injection of LPS.
Keyphrases
- inflammatory response
- chronic obstructive pulmonary disease
- septic shock
- lung function
- acute kidney injury
- intensive care unit
- pulmonary fibrosis
- lipopolysaccharide induced
- lps induced
- idiopathic pulmonary fibrosis
- toll like receptor
- anti inflammatory
- oxidative stress
- randomized controlled trial
- risk assessment
- immune response
- air pollution
- cystic fibrosis
- endothelial cells
- placebo controlled
- cell cycle arrest
- cell death
- ionic liquid
- high glucose
- phase iii
- signaling pathway
- diabetic rats
- phase ii
- extracorporeal membrane oxygenation