The Protective Effect of INH2BP, a Novel PARP Inhibitor 5-lodo-6-Amino-1,2-Benzopyrone, Against Hydrogen Peroxide-Induced Apoptosis Through ERK and p38 MAPK in H9c2 Cells

被引:8
|
作者
Back, Oun-Cheol [1 ,2 ]
Jang, Hyung-Seok [2 ]
Lee, Ji-Sook [3 ]
Kim, Dae-Eun [4 ]
Lee, Young [5 ]
Park, Eun-Seok [4 ]
Kim, In Sik [1 ,6 ]
机构
[1] Eulji Univ, Sch Med, Dept Biomed Lab Sci, Daejeon 301746, South Korea
[2] Hanyang Univ, Guri Hosp, Dept Pathol, Guri, Gyeonggi Do, South Korea
[3] Wonkwang Hlth Sci Univ, Dept Clin Lab Sci, Iksan, Jeollabuk Do, South Korea
[4] Kyungbok Univ, Dept Biomed Lab Sci, Pochen, South Korea
[5] Chungbuk Natl Univ, Dept Anim Sci, Cheongju, South Korea
[6] Eulji Univ, Grad Sch, Plus Program BK21, Dept Senior Healthcare, Daejeon 301746, South Korea
关键词
INH2BP; Reactive oxygen species; Apoptosis; POLY(ADP-RIBOSE) POLYMERASE INHIBITOR; OXIDATIVE STRESS; SUPEROXIDE-DISMUTASE; NAD(+) DEPLETION; HEME OXYGENASE-1; ACTIVATION; DEATH; SYNTHETASE; PATHWAY; KINASE;
D O I
10.1159/000439572
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
INH2BP (5-iodo-6-amino-1,2-benzopyrone), a poly-ADP ribose polymerase inhibitor, has been shown to possess anticancer, anti-viral, and anti-inflammation properties. The aim of this study was to investigate the protective effect of INH2BP against oxidative stress-induced apoptosis in H9c2 cardiomyoblast cells. While the treatment of H9c2 cardio-myoblasts cells with hydrogen peroxide (H2O2) caused a loss of cell viability and an increase in the number of apoptotic cells, INH2BP significantly protected the cells against H2O2-induced cell death without any cytotoxicity. Our data also shows that INH2BP significantly scavenged intracellular reactive oxygen species (ROS), and markedly enhanced the expression of antioxidant enzymes such as Mn-SOD (superoxide) and Cu/Zn-SOD, and heme oxygenase-1, which was accompanied by the concomitant activation of extracellular regulated kinase 1/2 (ERK1/2) and p38 mitogen-activated protein kinase (MAPK) phosphorylation in H9c2 cells. The effects of INH2BP on ERK1/2 and p38 MAPK phosphorylation were abrogated by PD98059, an ERK1/2 inhibitor, and 58203580, a p38 inhibitor. In addition, inhibition of ERK1/2 and p38 MAPK by these inhibitors significantly attenuated INH2BP-mediated H9c2 viability as well as cleaved caspases-3, Box, and Bcl-2 activation. Taken together, these results demonstrate that INH2BP prevents H2O2-induced apoptosis in H9c2 cells by reducing the production of intracellular ROS, regulating apoptotic-related proteins, and the activation of the ERK1/2 and p38 MAPK. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:259 / 270
页数:12
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