Change in expression of macrophage migration inhibitory factor mRNA in a rat model of ventilator-induced lung injury
Huijun Dai, Linghui Pan, Fei Lin, Wanyun Ge, Wei Li, Sheng He
Abstract
Huijun Dai, Linghui Pan, Fei Lin, Wanyun Ge, Wei Li, Sheng He
Abstract
Objective To investigate the changes in the expression of macrophage migration inhibitory factor (MIF) mRNA in a rat model of ventilator-induced lung injury. Methods Thirty adult male Sprague-Dawley rats, weighing 235-260 g, were randomly divided into 3 groups ( n = 10 each) using a random number table: con- trol group (group C), small tidal volume (VT ) mechanical ventilation group (group S) and large tidal volume me- chanical ventilation group (group L) . The animals were anesthetized with intraperitoneal ketamine 100 mg/kg, mi- dazolam 0.2 mg/kg and atropine 1.0 mg/kg. The rats were tracheostomized and spontaneous breathing was main- tained in group C, while the rats were tracheostomized and mechanically ventilated for 4 h in groups S and L. The tidal volume was 7 ml/kg (group S) or 40 ml/kg (group L),I: E was 1 : 1, RR was 80 bpm and FiO2 was 100% . At 4 h of spontaneous breathing or mechanical ventilation, broncho-alveolar lung lavage fluid (BALF) was collect- ed for determination of the total protein concentration; white blood cell (WBC) counts and concentrations of MIF, IL-6 and IL-1β (by ELISA). Then the rats were sacrificed and the lungs removed for microscopic examination and for determination of wet to dry lung weight ratio (W/D ratio) and expression of MIF mRNA (by RT-PCR). Results Compared with C and S groups, WBC counts, concentrations of total protein, MIF, IL-6 and IL-1β in BALF, and W/D ratio and expression of MIF mRNA in lung tissues were significantly increased in group L (P 〈 0.05). There was no significant difference in the indexes mentioned above between group C and group S ( P 〉 0.05 ). The pathological changes occurred in group L. Conclusion The up-regulation of MIF mRNA expression in lung tissues may be involved in the development of ventilator-induced lung injury in rats. Key words: Respiration, artificial; Respiratory distress syndrome, adult; Macrophage migration-in-
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Objective To investigate the changes in the expression of macrophage migration inhibitory factor (MIF) mRNA in a rat model of ventilator-induced lung injury. Methods Thirty adult male Sprague-Dawley rats, weighing 235-260 g, were randomly divided into 3 groups ( n = 10 each) using a random number table: con- trol group (group C), small tidal volume (VT ) mechanical ventilation group (group S) and large tidal volume me- chanical ventilation group (group L) . The animals were anesthetized with intraperitoneal ketamine 100 mg/kg, mi- dazolam 0.2 mg/kg and atropine 1.0 mg/kg. The rats were tracheostomized and spontaneous breathing was main- tained in group C, while the rats were tracheostomized and mechanically ventilated for 4 h in groups S and L. The tidal volume was 7 ml/kg (group S) or 40 ml/kg (group L),I: E was 1 : 1, RR was 80 bpm and FiO2 was 100% . At 4 h of spontaneous breathing or mechanical ventilation, broncho-alveolar lung lavage fluid (BALF) was collect- ed for determination of the total protein concentration; white blood cell (WBC) counts and concentrations of MIF, IL-6 and IL-1β (by ELISA). Then the rats were sacrificed and the lungs removed for microscopic examination and for determination of wet to dry lung weight ratio (W/D ratio) and expression of MIF mRNA (by RT-PCR). Results Compared with C and S groups, WBC counts, concentrations of total protein, MIF, IL-6 and IL-1β in BALF, and W/D ratio and expression of MIF mRNA in lung tissues were significantly increased in group L (P 〈 0.05). There was no significant difference in the indexes mentioned above between group C and group S ( P 〉 0.05 ). The pathological changes occurred in group L. Conclusion The up-regulation of MIF mRNA expression in lung tissues may be involved in the development of ventilator-induced lung injury in rats. Key words: Respiration, artificial; Respiratory distress syndrome, adult; Macrophage migration-in-
Key concepts: Tidal volume, Macrophage migration inhibitory factor, Lung, Ventilation (architecture), Mechanical ventilation, Andrology, Anesthesia, Intraperitoneal injection