LIU Qing-hui, YU Sen-yang. Protective effects of dexamethasone on ventilator-induced lung injury in an rat modelJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2003, 24(1): 16-18.
Citation: LIU Qing-hui, YU Sen-yang. Protective effects of dexamethasone on ventilator-induced lung injury in an rat modelJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2003, 24(1): 16-18.

Protective effects of dexamethasone on ventilator-induced lung injury in an rat model

  • Objective:To investigate the protective effects of dexamethasone on ventilator-induced lung injury(VILI)in an rat model. Methods:We established an rat model of VILI with a large tidal volume of 40m/l kg.After anesthesia was administered and tracheotomy was performed,30healthy male Sprague-Dawley rats were randomly divided into three groups to receive two ventilation protocols for 4h: group A was served as control groups (n=10,VT =8m/l kg),group B received large tidal volume ventilation (n=10,VT =40m/l kg),group C(n=10) received the same tidal volume as group B with pre-treatment of dexamethasone.Arterial blood gases were measured every one hour.Total white blood cells (WBCs) in BALF were counted.Wet to dry right lung weight ratio (W/D),the concentrations of total protein in bronchoalveolar lavage fluid (BALF),TNF-α,IL-1βlevels in BALF and blood.Lung histopathology was assessed among three groups.Results:After 4hrs mechanical ventilation,arterial oxygen pressure(PaO2) was significantly lower in group B than A and C.A large guantity of WBCs were found in BALF of group B.The total protein contents in BALF,W/D of right lung were significantly higher in group B than A and C.The levels of TNF-α,IL-1β in BALF were increased in group B,while decreased in group C.Histopathologic findings demonstrated more infiltrating WBCs ,destructive change of the alveolar wall in group B than other groups.Conclusions: These results suggest that a series of proinflammatory,inflammatory reactions may be involved in the course of VILI.Dexamethasone has obvious protective effects on VILI through its ant-i inflammation potents.
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