Babu G Nagesh, Sailor Kurt A, Beck Joseph, Sun Dandan, Dempsey Robert J
Department of Neurology, SGPG Institute of Medical Sciences, Lucknow, UP, 226014, India.
Neurochem Res. 2003 Dec;28(12):1851-7. doi: 10.1023/a:1026123809033.
Ornithine decarboxylase (ODC) is considered the rate-limiting enzyme in polyamine biosynthesis, and an increase in putrescine after central nervous system (CNS) injury appears to be involved in neuronal death. Cerebral ischemia and reperfusion trigger an active series of metabolic events, which eventually lead to neuronal death. In the present study, ODC activity was evaluated following transient focal cerebral ischemia and reperfusion in rat. The middle cerebral artery (MCA) was occluded for 2 h in male rats with an intraluminal suture technique. Animals were sacrificed between 3 and 48 h of reperfusion following MCA occlusion, and ODC activity was assayed in cortex and striatum. ODC activity was also estimated in an in vitro ischemia model using primary rat cortical neuron cultures, at 6-24 h reoxygenation following 1 h oxygen-glucose deprivation (OGD). In cortex, following ischemia, ODC activity was increased at 3 h (P < .05), reached peak levels by 6-9 h (P < .001) and returned to sham levels by 48 h reperfusion. In striatum the ODC activity followed a similar time course, but returned to basal levels by 24 h. This suggests that ODC activity is upregulated in rat CNS following transient focal ischemia and its time course of activation is region specific. In vitro, ODC activity showed a significant rise only at 24 h reoxygenation following ischemic insult. The release of lactate dehydrogenase (LDH), an indicator for cell damage, was also significantly elevated after OGD. 0.25 mM alpha-difluoromethylornithine (DFMO) inhibited ischemia-induced ODC activity, whereas a 10-mM dose of DFMO appears to provide some neuroprotection by suppressing both ODC activity and LDH release in neuronal cultures, suggesting the involvement of polyamines in the development of neuronal cell death.
鸟氨酸脱羧酶(ODC)被认为是多胺生物合成中的限速酶,中枢神经系统(CNS)损伤后腐胺增加似乎与神经元死亡有关。脑缺血再灌注引发一系列活跃的代谢事件,最终导致神经元死亡。在本研究中,对大鼠短暂局灶性脑缺血再灌注后的ODC活性进行了评估。采用腔内缝合技术将雄性大鼠大脑中动脉(MCA)闭塞2小时。在MCA闭塞后再灌注3至48小时之间处死动物,并在皮质和纹状体中测定ODC活性。还使用原代大鼠皮质神经元培养物在体外缺血模型中,于1小时氧糖剥夺(OGD)后复氧6至24小时时估计ODC活性。在皮质中,缺血后ODC活性在3小时时增加(P <.05),在6至9小时达到峰值水平(P <.001),并在再灌注48小时时恢复到假手术水平。在纹状体中,ODC活性遵循相似的时间进程,但在24小时时恢复到基础水平。这表明短暂局灶性缺血后大鼠中枢神经系统中ODC活性上调,其激活的时间进程具有区域特异性。在体外,缺血损伤后仅在复氧24小时时ODC活性显著升高。细胞损伤指标乳酸脱氢酶(LDH)的释放,在OGD后也显著升高。0.25 mMα-二氟甲基鸟氨酸(DFMO)抑制缺血诱导的ODC活性,而10 mM剂量的DFMO似乎通过抑制神经元培养物中的ODC活性和LDH释放提供一些神经保护作用,表明多胺参与神经元细胞死亡的发生。