Effects of dexmedetomidine hydrochloride on ERK1/2 activation in a rat model of ventilator-induced lung injury.
- Author:
Xin-gang HU
1
;
Xiang-cai RUAN
;
Lin YU
;
Ning DING
;
Shou-zhang SHE
;
Yu-lin LIAO
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Dexmedetomidine; therapeutic use; Extracellular Signal-Regulated MAP Kinases; metabolism; Male; Rats; Rats, Sprague-Dawley; Tumor Necrosis Factor-alpha; metabolism; Ventilator-Induced Lung Injury; drug therapy; enzymology
- From: Journal of Southern Medical University 2011;31(7):1252-1255
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effect of dexmedetomidine hydrochloride on inflammatory lung injury and phosphorylation of extracellular regulated protein (ERK1/2) in a rat model of ventilator-induced lung injury (VILI).
METHODSThirty-six adult male SD rats were randomized into 3 groups (n=12) to receive a 4-h standard ventilation (group C, with tidal volume of 8 ml/kg and respiratory rate of 90/min), high-tidal volume ventilation (group H, with tidal volume of 20 ml/kg and respiratory rate of 50 /min), and high-tidal volume ventilation plus 0.5 µg·kg(-1)·h(-1) dexmedetomidine infusion (group D), with the maintenance of a positive end expiratory pressure (PEEP) of 0 cmH(2)O. After mechanical ventilation the rats were sacrificed to collect the lung lavage liquid and lung tissue to examine the pulmonary inflammatory changes and tumor necrosis factor-α (TNF-α) expression as well as the expressions of ERK1/2 and p-ERK1/2.
RESULTSGroups H and D showed obvious lung injury and significant elevations of the total protein, WBC, MPO, TNF-α, and ERK1/2 phosphorylation as compared with those of group C. The rats in group D showed milder lung pathologies with significantly lower levels of phosphorylation of ERK1/2 and TNF-α compared with those in group H.
CONCLUSIONDexmedetomidine can significantly attenuate VILI, decrease the production of the inflammatory molecules, and inhibit the activation of ERK1/2, demonstrating a protective effect against VILI.