Modulation of Gene-Expression Profiles Associated with Sodium Arsenite-Induced Cardiotoxicity by p-Coumaric Acid, a Common Dietary Polyphenol

被引:12
作者
Prasanna, Nagalakshmi [1 ]
Rasool, Mahaboobkhan [1 ]
机构
[1] VIT Univ, Sch Bio Sci & Technol, Immunopathol Lab, Vellore 632014, Tamil Nadu, India
关键词
p-Coumaric Acid; Sodium Arsenite-Induced Cardiotoxicity; Inflammatory Mediators; Transcription Factors; Apoptotic proteins; OXIDATIVE STRESS; CANCER CELLS; COLON-CANCER; EXPOSURE; APOPTOSIS; PATHWAY; BCL-2; ATHEROSCLEROSIS; MITOCHONDRIA; BREAST;
D O I
10.1002/jbt.21550
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, the purpose was to investigate the effect of p-coumaric acid on the mRNA-expression levels of inflammatory cytokines, transcription factor, MAP kinases, and apoptotic proteins by real time reverse transcription polymerase chain reaction in the cardiac tissue of sodium arsenite exposed rats. Sodium arsenite administration (5 mg/kg/b.wt, once daily for 30 days) upregulated the mRNA-expression levels of inflammatory cytokines (interleukin-1 beta, interleukin-6, tumor necrosis factor-alpha, and tumor growth factor-beta), transcription factor (NF-Kb-Rel A), protein kinases (Janus kinase and p38), caspase 3, and proapoptotic protein Bax in the cardiac tissue of rats, but the antiapoptotic protein Bcl-2 mRNA expression was found be downregulated. However, p-coumaric acid (75, 100 mg/kg/b. wt. oral) pretreatment daily before the sodium arsenite exposure protected the changes in the above mRNA-expression profiles observed in the cardiac tissues. In conclusion, this study confirmed that p-coumaric acid could be a promising dietary agent for protecting against the sodium arsenite-induced cardiotoxicity.
引用
收藏
页码:174 / 180
页数:7
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