HS-FEN subverts detrimental effects elicited by Hpcf.

Abstract

Cellular expression of OPA-1 (a), Drp-1 (b) and SOD2 (c) genes detected by quantitative PCR performed on RNA extracted from AGS cells cultured for 3 hours with HS-FEN 25 μg mL-1 in presence or absence of Hpcf (1:2) stimulation. GAPDH was used as housekeeping gene to normalize all samples. Data were represented as means ± s.d. of three independent experiments, each performed in triplicate. One-way ANOVA followed by Bonferroni post hoc correction was used to determinate statistically significant differences (*** p <0.0001).</p