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Received December 19, 2011
Accepted March 20, 2012
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Effect of antioxidant in an acute lung injury animal model

Department of Pharmacology, College of Veterinary Medicine, Korea Zoonosis Research Institute, Chonbuk National University, 664-14 1-Ga Dukjin-dong, Dukjin-gu, Jeonju, Jeonbuk 561-756, Korea 1Division of Chemical Engineering, Chonbuk National University, 664-14 1-Ga Dukjin-dong, Dukjin-gu, Jeonju, Jeonbuk 561-756, Korea
kgb70@jbnu.ac.kr
Korean Journal of Chemical Engineering, November 2012, 29(11), 1591-1596(6), 10.1007/s11814-012-0041-0
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Abstract

The objective of this study was to scrutinize the involvement of nitric oxide (NO) and the diagnosis of blood in ARDS in a rat model determined by the sequential exposure to lipopolysaccharide (LPS). Also, the present study was designed to evaluate the effects of taurine and dexamethasone on ARDS induced by LPS. Measurements of nitrite/nitrate were elevated in BAL of LPS challenged rats, indicative of an induction of the NO synthase. Taurine and dexamethasone abrogated the extent of endotoxin-induced ARDS, as evidenced by the decreases BAL nitrate/nitrite, BALF protein and lung pathology. T+L+D-group had higher PaO2 and lower PaCO2 values than L-group and T+Lgroup. But, ionized Ca2+ and Mg2+ both were not shown significant change. Also, T+L and T+L+D-group showed significant increase compared with L-group, but for the other side no significant difference was seen between T+L and T+L+D group. We suggest that taurine and dexamethasone may be a drug of choice for preventing ARDS.

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