| The role of hydroxyl radical in the pathogenetic mechanism of endotoxin-induced acute lung injury in rats. |
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Young Soo Shim, Chul Gyu Yoo, Young Whan Kim, Sung Koo Han, Keun Youl Kim, Yong Chol Han |
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Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea |
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| Abstract |
Background
Although there have been many studies on the pathogenetic mechanism of acute lung injury, it is still elusive. Recently interests have been focused on the role of oxygen free radicals. But the effect of hydroxyl radical on the neutrophil mobilization and the alveolar-capillary permeability is not clear especially in the endotoxin-induced acute lung injury model of rats. This investigation was performed to evaluate the pathogenetic role of hydroxyl radical on the neutrophil accumulation into the lung and the increased alveolar-capillary permeability in the endotoxin-induced acute lung injury in rats.
Methods
Fifty rats were divided into four groups: vehicle control group (n=5, 6hrs; n=5, 24hrs), endotoxin-treated group (n=10, 6hrs; n=10, 24hr)， Dimetþylthiourea (DMTU)-pretreated group (n= 10, 6hrs), and deferoxamine (DFX)- pretreated group (n= 10, 6hrs). Thirty minutes before sacrifice, 125I-tagged bovine serum albumin was injected. Six and twenty four hours after endotoxin injection, the rats were sacrificed, and the radioactivity of lung tissue and peripheral blood was counted. Permeability index was defined as the ratio of radioactivity between lung tissue and peripheral blood. Another set of rats (n=52) were divided into the same four groups as before [vehicle control group (n=5, 6hrs; n=5, 24hrs), endotoxin-treated group (n=7, 6hrs; n=8, 24hrs), DMTU-pretreated group (n=6, 6hrs; n=9 , 24hrs), and DFX-pretreated group (n=5, 6hrs; n=7, 24hrs)] , and were sacrificed 6 and 24 hours after endotoxin injection- In these rats, cell profile of peripheral blood and bronchoalveolar lavage fluid was evaluated, and the pathologic examination of lung tissue was performed.
Results
1) Increased alveolar-capillary permeability was observed 6 hours after endotoxin injection, which was normalized after 24 hours, and this increase was attenuated by pretreatment with DMTU and DFX.
2) Neutrophil sequestration into the lung was observed 24 hours after endotoxin administration, but this was not influenced by DMTU and DFX pretreatment.
Conclusion
These results suggest that hydroxyl radical would not be involved in the sequestration of neutrophils into the lung, but plays an important role in the increase of alveolar-capillary permeability in the endotoxin-induced acute lung injury in rats. |
| Key Words:
Endotoxin, Hydroxyl radical, Acute lung injury, Rats |
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