基础医学与临床 ›› 2007, Vol. 27 ›› Issue (1): 44-48.

• 研究论文 • 上一篇    下一篇

II相酶诱导剂对选择性运动神经元损伤的保护作用

李哲(河北) 卜晖 刘晓云 李彬 孙萌萌 李春岩   

  1. 河北医科大学第二医院神经内科 河北医科大学第二医院神经内科 河北医科大学第二医院神经内科 河北医科大学第二医院神经内科
  • 收稿日期:2006-04-25 修回日期:2006-10-08 出版日期:2007-01-25 发布日期:2007-01-25
  • 通讯作者: 李哲(河北)

Involvement of COX-2 in effect of heme oxygenase-1 on cardioprotection from anocia/reoxygenation induced injury

  

  • Received:2006-04-25 Revised:2006-10-08 Online:2007-01-25 Published:2007-01-25

摘要: 目的 在选择性运动神经元损伤的脊髓片培养模型上,探讨Ⅱ相酶诱导剂CPDT(5,6-二氢环戊烯并1,2-二硫杂环戊烯-3-硫酮)对运动神经元的保护作用及机制。方法 乳大鼠脊髓片分为正常对照组、模型组(100μmol/L苏-羟天冬氨酸;THA)和Ⅱ相酶诱导剂CPDT(5、15和30μmol/L)干预组。以神经元特异性抗体SMI-32组化染色,对脊髓腹角α运动神经元进行鉴定、计数,并测定不同时间点培养液中乳酸脱氢酶(LDH)及丙二醛(MDA)含量。结果 THA使脊髓片腹角α运动神经元数目明显减少(P<0.01),培养液中LDH、MDA含量明显升高。与模型组相比,CPDT提前干预(15和30μmol/ L)可使α运动神经元数目明显增多(P<0.05),突起也较为丰富,培养液中LDH、MDA含量明显下降(P<0.05)。结论 Ⅱ相酶诱导剂CPDT可能通过抑制脂质过氧化物或清除自由基来抑制脊髓选择性运动神经元损伤。

Abstract: Objective To investigate the protection effect and mechanism of PhaseⅡenzyme inducer CPDT (5,6-dihydrocyclopenta[C]- 1, 2-dithiole-3-thione) against threo-hydroxyaspartate-induced injury of motor neuron in the cultured spinal cord slices of rats. Methods Organotypic spinal cord slices of rat pup was divided into normal control group, model group(THA 100μmol/L) and PhaseⅡenzyme inducer CPDT(5, 15, 30μmol/ L) treated groups. The morphology change of spinal cord slices was observed with inverted microscope. Ventralαmotor neurons' survivals were evaluated by immunohistochemical staining with monoclonal antibody SMI32, a nonphosphorylated neurofilament marker. Lactate dehydrogenase (LDH) and malonaldehyde (MDA) levels in culture medium were also measured. Results The slices of THA group showed that the number of Ventralαmotor neurons significantly decreased, but LDH enzyme activity and MDA level in culture medium increased. After CPDT(15, 30μmol/L) pretreatment, the spinal cord slices in vitro grew well and showed the similar change with the slices of normal control group. The number ofαmotor neurons significantly increased with intervention of CPDT, compared with model group. LDH and MDA level in culture medium also decreased. Conclusion PhaseⅡenzyme inducer, CPDT may inhibit THA-induced motor neuron injury by inhibiting lipid superoxide and scavenging free radical.