The Neuroprotective Potential of Phase II Enzyme Inducer on Motor Neuron Survival in Traumatic Spinal Cord Injury In vitro

被引:0
作者
Xiao-Yun Liu
Chun-Yan Li
Hui Bu
Zhe Li
Bin Li
Meng-Meng Sun
Yan-Su Guo
Li Zhang
Wen-Bo Ren
Zhi-Liang Fan
Dong-Xia Wu
Shu-Yu Wu
机构
[1] The Second Hospital of Hebei Medical University,Department of Neurology
[2] Institute of Cardiocerebrovascular Disease,undefined
来源
Cellular and Molecular Neurobiology | 2008年 / 28卷
关键词
Phase II enzyme inducer; Motor neuron; Spinal cord; Nuclear factor erythroid 2-related factor 2 (Nrf2); Heme oxygenase-1(HO-1);
D O I
暂无
中图分类号
学科分类号
摘要
(1) Phase II enzyme inducer is a kind of compound which can promote the expression of antioxidative enzymes through nuclear factor erythroid 2-related factor 2 (Nrf2) activation. Recently, it has been reported that these compounds show neuroprotective effect via combating oxidative stress. The purpose of this study is to determine whether phase II enzyme inducers have neuroprotective effects on traumatic spinal cord injury. (2) An organotypic spinal cord culture system was used, Phase II enzyme inducers were added to culture medium for 1 week, motor neurons were counted by SMI-32 staining, glutamate, Nrf2, and Heme oxygenase-1(HO-1) mRNA were tested. (3) This study showed motor neuron loss within 1 week in culture. After 1 week in culture, the system was stable. Moreover, Glutamate was increased when in culture 48 h and decreased after 1 week in culture. There was no significant change between 1 and 4 weeks in culture. Necrotic motor neuron and damaged mitochondrial were observed in culture 48 h. Furthermore, phase II enzyme inducers: tert-butyhydroquinone (t-BHQ), 3H-1,2-dithiole-3-thione (D3T), and 5,6-dihydrocyclopenta-1,2-dithiole-3-thione (CPDT) were shown to promote motor neuron survival after dissection, it was due to increasing Nrf2 and HO-1 mRNA expression and protecting mitochondrial not due to decreasing glutamate level. (4) The loss of motor neuron due to dissection can mimic severe traumatic spinal cord injury. These results demonstrate that glutamate excitotoxicity and the damage of mitochondrial is possibly involve in motor neuron death after traumatic spinal cord injury and phase II enzyme inducers show neuroprotective potential on motor neuron survival in traumatic spinal cord injury in vitro.
引用
收藏
页码:769 / 779
页数:10
相关论文
共 116 条
  • [11] Hallur S(2001)Protein and DNA oxidation in spinal injury: neurofilaments—an oxidation target Free Radic Biol Med 30 613-624
  • [12] Qiu HZ(2006)Structure-activity relationships in the induction of Phase II enzymes by derivatives of 3H-1, 2-dithiole-3-thione in rats Chem Biol Interact 160 115-122
  • [13] Peng X(1996)Excitotoxicity and excitoprotection in vitro Adv Neurol 71 1-37
  • [14] Li Y(1998)Induction of heme oxygenase-1 (HO-1) in the contused spinal cord of the rat Brain Res 795 17-24
  • [15] Dykens JA(2000)Co-induction of HSP70 and heme oxygenase-1 in macrophages and glia after spinal cord contusion in the rat Brain Res 883 233-237
  • [16] Stern A(2002)Enhanced expression of the transcription factor Nrf2 by cancer chemopreventive agents: role of antioxidant response element-like sequences in the nrf2 promotor. Mol Cell Biol 22 2883-2892
  • [17] Trenkner E(2003)Modulation of gene expression by cancer chemopreventive dithiolethiones through the Keap1-Nrf2 pathway. J Biol Chem 278 8135-8145
  • [18] Fahey JW(2002)NBQX treatment improves mitochondrial function and reduces oxidative events after spinal cord injury J Neurotrauma 19 917-927
  • [19] Talalay P(1994)Late-onset selective neuronal damage in the rat spinal cord induced by continuous intrathecal administration of AMPA Brain Res 654 279-285
  • [20] Hall ED(2003)Disruption of glial glutamate transport by reactive oxygen species produced in motor neurons J Neurosci 23 2627-2633