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Chinese Journal of Applied Physiology ; (6): 293-296, 2019.
Article in Chinese | WPRIM | ID: wpr-776512

ABSTRACT

OBJECTIVE@#To investigate the effects of vitamin E on the respiratory function impairment in rats with chronic obstructive pulmonary disease (COPD) after exposed to high temperature and PM.@*METHODS@#Fifty-four 7-week-old SPF male Wistar rats were randomly divided into 9 experimental groups (n=6). The rat COPD model was established by lipopolysaccharide (LPS) and smoke exposure. After modeled, the rats were tracheal instilled with PM (0 mg/ml, 3.2 mg/ml) and intraperitoneally injected with vitamin E at the dose of 40 mg/kg (20 mg/ml). Part of rats (high temperature groups) were then exposed to high temperature (40℃), once (8 h) a day for three consecutive days. After the last exposure, the lung function of rats was detected. The expression levels of inducible nitric oxide synthase (iNOS), tumor necrosis factor-α (TNF-α) and monocyte chemotactic protein-1 (MCP-1) were detected by corresponding ELISA kits.@*RESULTS@#Compared with the control group, exposure of high temperature and PM could inhibit the lung function of COPD rats significantly (P<0.05); the level of MCP-1 was increased significantly in PM-exposure groups (P<0.05); iNOS was increased significantly in the groups of high temperature (P<0.05). Compared with the single-PM exposure groups, TNF-α in lung was decreased in the normal temperature health group and high temperature COPD group (P<0.05) after treated with vitamin E; MCP-1 was decreased in all vitamin E-treated groups (P<0.05); the decreased iNOS only appeared in the group of high temperature with vitamin E treatment.@*CONCLUSION@#High temperature and PM could aggravate the inflammation of COPD rats. As an antioxidant, vitamin E may protect the lung from the damage effects.


Subject(s)
Animals , Male , Rats , Chemokine CCL2 , Metabolism , Hot Temperature , Lung , Nitric Oxide Synthase Type II , Metabolism , Particulate Matter , Pulmonary Disease, Chronic Obstructive , Drug Therapy , Random Allocation , Rats, Wistar , Tumor Necrosis Factor-alpha , Metabolism , Vitamin E , Pharmacology
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