Protective effect of 3-butyl-6-bromo-1(3H)-isobenzofuranone on hydrogen peroxide-induced damage in PC12 cells

被引:26
作者
Gao, Yuan [1 ]
Zhang, Hong-Wei [1 ]
Qiao, Hai-Ling [1 ]
Wang, Wei [1 ]
Chang, Jun-Biao [1 ]
机构
[1] Zhengzhou Univ, Sch Med, Dept Clin Pharmacol, Zhengzhou 450052, Henan, Peoples R China
关键词
3-butyl-6-bromo-1(3H)-isobenzofuranone; Oxidative stress; ROS; MMP; Ca2(+)](i); Apoptosis; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; APOPTOSIS; BRAIN; PEROXYNITRITE; DEPRIVATION; GLUTATHIONE; SUPEROXIDE; MECHANISM; DOPAMINE;
D O I
10.1016/j.brainres.2010.08.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative stress, an imbalance toward the prooxidant side of the prooxidant/antioxidant homeostasis, occurs in several brain neurodegenerative disorders. The protective effect of 3butyl-6-bromo-1(3H)-isobenzofuranone (Br-NBP), a derivative compound of 1-3-n-butylphthalide (NBP), on the hydrogen peroxide(H2O2)- induced oxidative damage was investigated in PC12 cells. Following exposure of the cells to H2O2, there was a significant reduction in cell survival,activities of glutathione peroxidase (GSH-px) and mitochondria membrane potential(MMP), in contrast, the increased levels in the leakage of lactate dehydrogenase (LDH), malondialdehyde (MDA) contents, nitric oxide (NO) productions, intracellular reactive oxygen species (ROS), intracellular Ca2+. concentration ([Ca2+](i)), as well as cell apoptosis were observed. However, pretreatment of cells with Br-NBP prior to H2O2 exposure attenuated all the changes mentioned above in a concentration-dependent manner except no effect on activities of GSH-px. Br-NBP exhibited the protective effect against H2O2-induced cytotoxicity in PC12 cells, suggesting that the compound may be a potential therapeutic agent for diseases induced by oxidative damage. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 247
页数:9
相关论文
共 35 条
  • [1] Nitric oxide and promotion of cardiac myocyte apoptosis
    Andréka, P
    Tran, T
    Webster, KA
    Bishopric, NH
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 263 (01) : 35 - 53
  • [2] Bishopric Nanette H., 2001, Current Opinion in Pharmacology, V1, P141, DOI 10.1016/S1471-4892(01)00032-7
  • [3] Pathological apoptosis in the developing brain
    Blomgren, Klas
    Leist, Marcel
    Groc, Laurent
    [J]. APOPTOSIS, 2007, 12 (05) : 993 - 1010
  • [4] APOPTOSIS AND NECROSIS - 2 DISTINCT EVENTS INDUCED, RESPECTIVELY, BY MILD AND INTENSE INSULTS WITH N-METHYL-D-ASPARTATE OR NITRIC-OXIDE SUPEROXIDE IN CORTICAL CELL-CULTURES
    BONFOCO, E
    KRAINC, D
    ANKARCRONA, M
    NICOTERA, P
    LIPTON, SA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7162 - 7166
  • [5] Free radicals and the pathobiology of brain dopamine systems
    Cadet, JL
    Brannock, C
    [J]. NEUROCHEMISTRY INTERNATIONAL, 1998, 32 (02) : 117 - 131
  • [6] Chang Q, 2003, ACTA PHARMACOL SIN, V24, P796
  • [7] NITRIC-OXIDE MODULATES AGONIST-EVOKED CA2+ RELEASE AND INFLUX RESPONSES IN PC12-64 CELLS
    CLEMENTI, E
    VECCHIO, I
    CORASANITI, MT
    NISTICO, G
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 289 (01): : 113 - 123
  • [8] Estévez AG, 1998, J NEUROSCI, V18, P923
  • [9] ESTEVEZ AG, 1995, J NEUROCHEM, V65, P1543
  • [10] FLOHE L, 1984, METHOD ENZYMOL, V105, P114