Pioglitazone Inhibits the Expressions of p22phox and p47phox in Rat Mesangial Cells In Vitro. (3rd February 2014)

• Record Type: Journal Article
• Authors: Wang, Shan; Ye, Shan-dong; Sun, Wen-jia; Hu, Yuan-yuan
• Other Names: Chan W. B. Academic Editor.; Fürnsinn C. Academic Editor.
• Is Part Of: ISRN endocrinology. Volume 2014(2014)
• Publication Date: 2014-02-03
• Subjects: Endocrinology -- Periodicals; Endocrine System Diseases; Endocrinology; Endocrinology; Electronic journals; Periodical; Fulltext; Internet Resources; Periodicals; Periodicals; 616.4
• DOI: 10.1155/2014/601352
• Languages: English
• ISSNs: 2090-4630

Abstract

Abstract : Aim . The purpose of this study was to investigate the effects of pioglitazone on oxidative stress and the expressions of p22 phox and p47 phox, subunits of NADPH oxidase, in mesangial cells (MCs). Method . Rat mesangial cells were cultured and randomly divided into normal glucose (NG) group, high glucose (HG) group, and pioglitazone group. After 48 h exposure, the supernatants and cells were collected. The expressions of p22 phox and p47 phox in MCs were detected by RT-PCR and western blot. The levels of intracellular ROS were determined by flow cytometry. Coloimetry method was used to detect malondialdehyde (MDA) concentrations and superoxide dismutase (SOD) activities. Results . Compared with the NG group, the expression levels of p22 phox, p47 phox and ROS significantly increased, the activity of SOD decreased in HG group, while the concentration of MDA greatly increased (P < 0.01 ). Pioglitazone significantly suppressed HG-induced p22 phox and p47 phox expressions and oxidative stress. The protein and gene expressions of p22 phox and p47 phox were markedly reduced after pioglitazone treatment, so did the ROS generation. The activities of SOD in MCs increased, while the concentrations of MDA in the supernatant decreased greatly by pioglitazone. Conclusions . Pioglitazone can inhibit HG-induced oxidative stress in MCs through suppressing p22 phox and p47 phox expressions.