Losartan regulates oxidative stress via caveolin-1 and NOX4 in mice with ventilator- induced lung injury.
- Author:
Xuguang LING
1
;
Anni LOU
;
Yang LI
;
Renqiang YANG
;
Zuowei NING
;
Xu LI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Caveolin 1; metabolism; Losartan; pharmacology; Lung; metabolism; physiopathology; Male; Mice; Mice, Inbred C57BL; NADPH Oxidase 4; NADPH Oxidases; metabolism; Oxidative Stress; Respiration, Artificial; Ventilator-Induced Lung Injury; drug therapy; metabolism
- From: Journal of Southern Medical University 2015;35(12):1739-1744
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effect of losartan in regulating oxidative stress and the underlying mechanism in mice with ventilator-induced lung injury.
METHODSThirty-six male C57 mice were randomly divided into control group, losartan treatment group, mechanical ventilation model group, and ventilation plus losartan treatment group. After the corresponding treatments, the lung injuries in each group were examined and the expressions of caveolin-1 and NOX4 in the lung tissues were detected.
RESULTSThe mean Smith score of lung injury was significantly higher in mechanical ventilation model group (3.3) than in the control group (0.4), and losartan treatment group (0.3); the mean score was significantly lowered in ventilation plus losartan treatment group (2.3) compared with that in the model group (P<0.05). The expressions of caveolin-1 and NOX4 were significantly higher in the model group than in the control and losartan treatment groups (P<0.05) but was obviously lowered after losartan treatment (P<0.05). Co-expression of caveolin-1 and NOX4 in the lungs was observed in the model group, and was significantly decreased after losartan treatment.
CONCLUSIONLosartan can alleviate ventilator-induced lung injury in mice and inhibit the expression of caveolin-1 and NOX4 and their interaction in the lungs.
