Deng X, Wang Y, Chou J, Cadet J L
NIH/NIDA-IRP, 5500 Nathan Shock Drive, Baltimore, MD 21224, USA.
Brain Res Mol Brain Res. 2001 Sep 10;93(1):64-9. doi: 10.1016/s0169-328x(01)00184-x.
Terminal deoxynucleotidyl transferase (TdT)-mediated dNTP nick end labeling (TUNEL) histochemistry is a sensitive method to expose DNA strand breaks in apoptotic cells, but it is difficult to conduct on slide-mounted sections. By using a 80 degrees C/0.5% Triton X-100 pretreatment, we have developed a TUNEL histochemical approach with high specificity and sensitivity using sections from ischemic rat brains. Thereafter, methamphetamine (METH)-induced neuronal death was investigated in mice brains. The results showed that a single injection of 40 mg/kg METH caused neuronal death in several brain areas including the striatum, cortex (frontal, parietal, and piriform), indusium griseum, medial habenular nucleus, and hippocampus. These results further confirmed the presence of METH-induced deleterious effects in nondopaminergic neurons. The significance of these findings is also discussed.
末端脱氧核苷酸转移酶(TdT)介导的dNTP缺口末端标记(TUNEL)组织化学是一种用于揭示凋亡细胞中DNA链断裂的灵敏方法,但在载玻片上的切片上进行操作较为困难。通过使用80℃/0.5% Triton X - 100预处理,我们利用缺血大鼠脑切片开发出了一种具有高特异性和灵敏度的TUNEL组织化学方法。此后,研究了甲基苯丙胺(METH)诱导的小鼠脑神经元死亡。结果显示,单次注射40 mg/kg METH会导致包括纹状体、皮质(额叶、顶叶和梨状叶)、灰被、内侧缰核和海马体在内的多个脑区的神经元死亡。这些结果进一步证实了METH对非多巴胺能神经元具有有害作用。还讨论了这些发现的意义。