Kazahari S, Takizawa S, Ogawa S, Habu S, Shinohara Y
Department of Neurology, School of Medicine, Tokai University, Kanagawa, Japan.
Rinsho Shinkeigaku. 1996 Mar;36(3):451-5.
To clarify whether programmed cell death plays an important role in the delayed neuronal death after forebrain transient ischemia, we investigated the relationship between pathological changes visualized by HE staining and intranuclear DNA fragmentation evaluated by the TUNEL method in rat hippocampal CA1 pyramidal neurons at early times after the onset of transient forebrain ischemia. The investigations were carried out in male Wistar rats (N = 22) subjected to 20 minutes of transient forebrain ischemia by Pulsinelli's method. No morphological changes or TUNEL staining were observed at 1 hour after forebrain ischemia. HE staining revealed morphological changes in 8 +/- 4%, 10 +/- 4% and 88 +/- 9% of neurons in hippocampus CA1 at 3, 6 and 24 hours after forebrain ischemia, respectively at which times 0%, 74 +/- 1% and 68 +/- 11% of the neurons showed marked labeling with the TUNEL method. We therefore conclude that DNA fragmentation as evaluated by the TUNEL method is not involved in neuronal death, and no DNA fragmentation was detectable prior to morphological changes in the early stage of forebrain ischemia.
为了阐明程序性细胞死亡在前脑短暂性缺血后延迟性神经元死亡中是否起重要作用,我们研究了在前脑短暂性缺血发作后的早期,通过苏木精-伊红(HE)染色观察到的病理变化与通过末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)法评估的核内DNA片段化之间的关系。研究在采用普尔西内利方法进行20分钟前脑短暂性缺血的雄性Wistar大鼠(N = 22)中进行。在前脑缺血后1小时未观察到形态学变化或TUNEL染色。HE染色显示,在前脑缺血后3、6和24小时,海马CA1区分别有8±4%、10±4%和88±9%的神经元出现形态学变化,而在这些时间点,采用TUNEL法检测到分别有0%、74±1%和68±11%的神经元呈现明显标记。因此,我们得出结论,通过TUNEL法评估的DNA片段化与神经元死亡无关,并且在前脑缺血早期形态学变化之前未检测到DNA片段化。