Objective:To investigate the immune protection and mechanism of naloxone hydrochloride on rats with acute respiratory distress syndrome (ARDS). Methods:Thirty healthy SD rats were randomly divided into control group, model group, and naloxone group,each group had ten rats. Control group:1.15 ml·kg-1 normal saline was administrated by femoral vein injection. Model group:1.0 ml·kg-1 normal saline was administrated by femoral vein injection after 0.15 ml·kg-1 oleic acid was administrated. Naloxone group:1.0 ml·kg-1 naloxone hydrochloride was administrated by femoral vein injection after 0.15 ml·kg-1 oleic acid was administrated. The ratio of left lung wet/dry weight was calculated.β-endorphins and T-lymphocyte subsets in plasma was determined,and the content of TNF-α, IL-1β, IL-6, IL-8 were determined by enzyme linked immunosorbent assay(ELISA).Results:Compared with control group, Left lung wet/dry weight ratio, the level of β-endorphins, CD3+, CD4+, CD4+/CD8+, TNF-α, IL-1β, IL-6, IL-8 of rats in ARDS model group were significantly increased, CD8+ was significantly lower than control group(P<0.05).Compared with model group, Left lung wet/dry weight ratio, the level of β-endorphins,CD8+, TNF-α, IL-1β, IL-6, IL-8 of rats in naloxone group were significantly decreased, CD3+, CD4+ and CD4+/CD8+ were significantly increased (P<0.05).Conclusion:Naloxone hydrochloride can protect body from ARDS by inhibiting plasma β-Endorphins,adjecting T-lymphocyte subsets, reducing body inflammation and alveolar edema. |
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