Abstract

<p>(A) HK-2 cells were pretreated with 10 µM rosiglitazone in the absence or presence of 100 µM GW9662 for 2 hours and then treated with 1 μg/ml LPS for 30 minutes. Equal amounts of nuclear extracts were assayed for binding a biotin-labeled double-stranded NF-κB oligonucleotide as described in 'Material and Methods'. The positions of NF-κB p65 was indicated. The column bar graph shows the means ± SD of values obtained by EMSAs densitometric analysis from three independent experiments. *<i>P</i><0.05 compared to the control group; <sup><i>#</i></sup><i>P</i><0.05 compared to the LPS-treated group; <sup><i>&</i></sup><i>P</i><0.05 compared to LPS + RGL (10 µM)-treated group.</p

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