into 4-m-thick sections. Sections were stained first with Mayer’s hematoxylin and then with a 1% eosin alcohol solution. HE PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19713189 staining samples were mounted with malinol and inspected with the aid of a microscope. The histological severity of lung was blindly scored R-roscovitine site followed by previous reports partly modified. Measurement of virus titer Lungs from mice on day 7 after virus infection were collected and homogenized in 2 ml of RPMI 1640 medium. Virus titers were determined by a plaque assay on MDCK cells. MDCK cells were seeded on a 24 well culture plate and cultured until reaching confluency. Cells were washed with PBS, and then 0.1-ml amounts of each dilution were inoculated to cultured cell followed by incubation for 1 h at 34C. DMEM containing 100 U/mL penicillin, 100 g/ml streptomycin and 0.5 g/ml fungizone was added to each well and incubated at 37C for 3 days in a humidified incubator with 5% CO2. The 
cytopathological effect was calculated 4 / 16 Levofloxacin Protects against Influenza Virus-Induced Lung Injury and 50% tissue PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19709857 culture infectious dose was calculated using the formula developed by Reed and Muench. Immunostaining of lung tissue On day 7 after virus infection, the mice were sacrificed and whole lungs were removed under anesthesia with diethyl ether. The removed lungs were fixed in 4% buffered paraformaldehyde and then embedded in paraffin, which were then cut into 4-m-thick sections. After antigen activation with immunosaver, a solution containing 50 mM Tris/HCl + 0.1% Tween-20 was used to solubilize the lung slices, followed by blocking with Block Ace at room temperature for 15 min. The primary antibody reaction was then conducted below 4C overnight. The primary antibody containing 8-hydroxy-2′-deoxygenase and nitrotyrosine was diluted 50 times before use. The lung slices were then washed with 50 mM Tris/HCl and 0.1% Tween-TB, followed by the secondary antibody reaction at 25C for 1.5 h. For the secondary antibody of NO2-Tyr and 8-OH-dG, Alexa Fluor 546 goat anti-mouse IgG and Alexa Fluor 488 goat anti-mouse IgG were diluted 200 times, respectively. After the reaction, the slide was observed by microscopy. Image analyses of the extent and intensity of 8-OH-dG and NO2-Tyr staining were also performed using the imageJ software. d-ROMs test Whole blood was obtained from mice under anesthesia with diethyl ether on day 7 after administration of the influenza virus. Whole blood was centrifuged at 1,000 g for 10 min and the resulting serum was used for the assay. Derivatives of reactive oxidative metabolites were assayed using FREE carpe diem following the manufacturer’s recommended protocols. Measurement of NO and IFN- in BALF The mice were anesthetized with diethyl ether, the chests were opened on day 7 after administration of the influenza virus. BALF was collected by cannulating the trachea with 1 ml of sterile PBS containing heparin. About 1.8 ml of BALF was routinely recovered from each animal after 2 lavages. The BALF was centrifuged at 4,100 g for 5 min at 4C to separate the cells in the BALF from the liquid. The supernatant was used in the assay. Nitrate and nitrite were measured using an EiCOM ENO-20 NOx analyzer. The mobile phase was NOCARA and reaction solution was comprised of Griess reagents. Equal concentrations of a mixture of NaNO2 and NaNO3 were used to prepare a standard curve. Serum IFN- was measured using an ELISA MAX Deluxe Set following the manufacturer’s protocols. Data analysis Data are the mean SD in ea