Deciphering the the role of ferulic acid against streptozotocin-induced cellular stress in the cardiac tissue of diabetic rats

被引:89
作者
Chowdhury, Sayantani [1 ]
Ghosh, Sumit [1 ]
Rashid, Kahkashan [1 ]
Sil, Parames C. [1 ]
机构
[1] Bose Inst, Div Mol Med, P-1-12,CIT Scheme 7 M, Kolkata 700054, W Bengal, India
关键词
STZ-induced diabetes; Cardiac dysfunction; Hyperglycemia; Oxidative and ER stress; Apoptosis; Ferulic acid; ENDOPLASMIC-RETICULUM STRESS; NF-KAPPA-B; RED-BLOOD-CELLS; OXIDATIVE STRESS; PROTECTIVE ROLE; ORGAN PATHOPHYSIOLOGY; LIPID-PEROXIDATION; ARJUNOLIC ACID; SHORT-TERM; INSULIN-RESISTANCE;
D O I
10.1016/j.fct.2016.09.011
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The cardiomyocytes are one of the major sources of hyperglycemia induced ROS generation. The present study focuses on the ameliorative role of ferulic acid in combating cardiac complications in diabetic rats. Induction of diabetes by STZ in male Wistar rats (at a dose of 50 mg kg(-1) body wt, i.p.) reduced body weight and plasma insulin level, enhanced blood glucose, disturbed the intra-cellular antioxidant machineries and disintegrated the normal radiation pattern of cardiac muscle fibers. Induction of ER stress (up-regulation in the levels of CHOP, GRP78, elF2 alpha signaling, increased calpain-1 expression), caspase-3 activation, PARP cleavage and DNA fragmentation were evidenced from immunoblot analyses and DNA fragmentation assay. However, ferulic acid administration, (at a dose of 50 mg kg(-1) body wt, orally for eight weeks) in post-hyperglycemia could reverse such adverse effects. Also, the molecule increased GLUT-4 translocation to the cardiac membrane by enhanced phosphorylation of PI3Kinase, AKT and inactivation of GSK-3 beta thereby altering the hyperglycemic condition in the cardiac tissue of diabetic rats. Therefore, as a potential therapeutic, ferulic acid, exhibiting antioxidant and hypoglycemic effects, may hold promise in circumventing stress mediated diabetic cardiomyopathy in rats. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:187 / 198
页数:12
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