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
相关论文
共 44 条
[21]  
Korsmeyer SJ, 1999, CANCER RES, V59, p1693S
[22]   ALS-linked Cu/Zn-SOD mutation increases vulnerability of motor neurons to excitotoxicity by a mechanism involving increased oxidative stress and perturbed calcium homeostasis [J].
Kruman, II ;
Pedersen, WA ;
Springer, JE ;
Mattson, MP .
EXPERIMENTAL NEUROLOGY, 1999, 160 (01) :28-39
[23]   Heme oxygenase-1 mediates the anti-inflammatory effect of interleukin-10 in mice [J].
Lee, TS ;
Chau, LY .
NATURE MEDICINE, 2002, 8 (03) :240-246
[24]   Myocardial ischemic preconditioning in rodents is dependent on poly (ADP-ribose) synthetase [J].
Liaudet, L ;
Yang, ZQ ;
Al-Affar, EB ;
Szabó, C .
MOLECULAR MEDICINE, 2001, 7 (06) :406-417
[25]   Decrease in manganese superoxide dismutase leads to reduced root growth and affects tricarboxylic acid cycle flux and mitochondrial redox homeostasis [J].
Morgan, Megan J. ;
Lehmann, Martin ;
Schwarzlaender, Markus ;
Baxter, Charles J. ;
Sienkiewicz-Porzucek, Agata ;
Williams, Thomas C. R. ;
Schauer, Nicolas ;
Fernie, Alisdair R. ;
Fricker, Mark D. ;
Ratcliffe, R. George ;
Sweetlove, Lee J. ;
Finkemeier, Iris .
PLANT PHYSIOLOGY, 2008, 147 (01) :101-114
[26]   MAPK signalling in cardiovascular health and disease: molecular mechanisms and therapeutic targets [J].
Muslin, Anthony J. .
CLINICAL SCIENCE, 2008, 115 (7-8) :203-218
[27]   Oxidation of biological systems: Oxidative stress phenomena, antioxidants, redox reactions, and methods for their quantification [J].
Nyska, A ;
Kohen, R .
TOXICOLOGIC PATHOLOGY, 2002, 30 (06) :620-650
[28]  
Pacher P, 2006, INT J MOL MED, V17, P369
[29]   Cardioprotective effects of rhamnetin in H9c2 cardiomyoblast cells under H2O2-induced apoptosis [J].
Park, Eun-Seok ;
Kang, Jun Chul ;
Jang, Yong Chang ;
Park, Jong Seok ;
Jang, Shin Yi ;
Kim, Dae-Eun ;
Kim, Bokyung ;
Shin, Hwa-Sup .
JOURNAL OF ETHNOPHARMACOLOGY, 2014, 153 (03) :552-560
[30]   Protective effect of the poly(ADP-ribose) polymerase inhibitor PJ34 on mitochondrial depolarization-mediated cell death in hepatocellular carcinoma cells involves attenuation of c-Jun N-terminal kinase-2 and protein kinase B/Akt activation [J].
Radnai, Balazs ;
Antus, Csenge ;
Racz, Boglarka ;
Engelmann, Peter ;
Priber, Janos Krisztian ;
Tucsek, Zsuzsanna ;
Veres, Balazs ;
Turi, Zsuzsanna ;
Lorand, Tamas ;
Sumegi, Balazs ;
Gallyas, Ferenc, Jr. .
MOLECULAR CANCER, 2012, 11