All samples were measured for their individual levels, and each sample was analyzed in triplicate manner, taking the mean of the three determinations. For PAS staining, histochemical staining of glycoconjugates was carried out as per the method of Pandurangan et al.,[14] using 2% PAS’ reagent

in dark for 20 min. Apoptotic cells in the mTOR inhibitor gastric mucosa were detected using the In Situ Cell Apoptosis Detection kit (Promega, Madison, WI, USA), with at least three replicates for each group. Immunohistochemistry was performed on replicate sections of mouse colon tissues. Sections fixed in 10% buffered formalin and embedded in paraffin were deparaffinized, rehydrated, and boiled three times in 100 mM Tris-buffered saline (pH 7.6) with 5% urea in an 850 W microwave oven for 5 min each. Sections were also incubated with F4/80 and CD31 antibody in the presence of 1.0% bovine serum albumin and finally incubated for 16 h at 4°C. The sections were counterstained with hematoxylin. Various concentrations of SAC were added to a Navitoclax molecular weight total volume of 200 μl containing 0.05 mM FeSO4, 1 mM H2O2, 1 mM 5,5-dimethylpyrroline-N-oxide (DMPO, Sigma), 5-tert-Butoxycarbonyl-5-methyl-1-pyrroline-N-oxide(BMPO, Enzo, Plymouth Meeting, PA, USA), and 50 mM, sodium phosphate at pH 7.4 at room temperature. Reactions were initiated by adding H2O2.

After incubation for 1 min, aliquots of the reactions were transferred to a quartz cell, and the spectrum of DMPO-OH and BMPO-OH was examined using an ESR spectrophotometer

(JES-TE300, JEOL, Tokyo, Japan), under the following conditions: magnetic field, 338.0 ± 5.0 mT; microwave power, 4.95 mW; frequency, 9.421700 GHz; modulation amplitude, 5 mT; sweep time, 0.5 min; and time constant, 0.03 s. The rat gastric mucosal cells, RGM1, were kindly given by Prof. Hirofumi Matsui (University of Tsukuba, Japan) and were maintained at 37°C in 上海皓元医药股份有限公司 a humidified atmosphere containing 5% CO2 and cultured in Dulbecco’s modified Eagle’s medium containing 10% (v/v) fetal bovine serum and 100 U/mL penicillin. RGM1 cells were seeded in a 100-mm dish and grown to 80% confluence in the complete growth medium. The cells were treated with SAC. After 6 h, the cells were further treated with TNF-α for 3 h (nuclear extracts), 6 h (RNA), and 24 h (whole cell lysates). The cells were then washed with PBS and lysed, and the cells were treated with several inhibitors. After 1 h, the cells were further treated with TNF-α for 1 h and for 24 h. The cells were then washed with PBS and lysed. After incubation, media was removed by suction and cells were washed with PBS twice. RiboEX (500 μL; GeneAll, Seoul, Korea) was added to plates, which were then incubated for 10 min at 4°C. RiboEX was harvested and placed in a 1.5-mL tube, and 100 μL of chloroform was added and gently mixed. After incubation for 10 min in ice, samples were centrifuged at 10 000 × g for 30 min.