Guglielmo M A, Chan P T, Cortez S, Stopa E G, McMillan P, Johanson C E, Epstein M, Doberstein C E
Department of Neurosurgery, Brown University School of Medicine, Providence, RI, USA.
Neurol Res. 1998 Jun;20(4):283-96. doi: 10.1080/01616412.1998.11740520.
Although neuronal death has been studied in experimental models of ischemia, the precise mechanisms regulating cell death remain unclear. Furthermore, the timing and pattern of neuronal death in human stroke has not been extensively studied. To further our understanding of ischemia-induced neuronal death, we examined the temporal profile of histochemical and morphologic characteristics of hippocampal neuronal death following experimental forebrain ischemia and compared these findings to human brain specimens obtained from subjects suffering cerebral infarction. Transient forebrain ischemia (TFI) was induced in normothermic adult rats by bilateral carotid artery occlusion combined with hypotension. Animals were sacrificed at 6, 12, 18, 24, 48, and 72 h and 7, 14, and 28 days following ischemia (n = 4 at each time point). Experimental tissue was analyzed using light and electron microscopy as well as TUNEL histochemistry. A total of 27 human brain specimens with neuropathological confirmation of ischemic damage and appropriate controls were also examined using light microscopy and TUNEL histochemistry. Dense TUNEL staining in hippocampal CA-1 neurons was present at 48 and 72 h following experimental ischemia. Prior to these times, little or no nuclear staining was noted and after 72 h nuclear staining diminished rapidly. Ultrastructural findings at these time points demonstrated many features similar to those seen in cells undergoing apoptosis, such as cell shrinkage with increased electron density, chromatin condensation with formation of heterochromatin, intact plasma membranes, and intact intracellular organelles. In a similar fashion, human stroke specimens during the subacute period showed dense nuclear TUNEL staining in penumbral neurons, whereas in the acute or chronic stages little or no staining was noted. Our results demonstrate that the timing of morphologic changes and TUNEL histochemistry following human stroke resembles that observed in experimental TFI. Furthermore, neuronal death in both experimental ischemia and human stroke share several features characteristic of apoptotic cell death.
尽管在缺血实验模型中已对神经元死亡进行了研究,但调节细胞死亡的精确机制仍不清楚。此外,人类中风中神经元死亡的时间和模式尚未得到广泛研究。为了进一步了解缺血诱导的神经元死亡,我们检查了实验性前脑缺血后海马神经元死亡的组织化学和形态学特征的时间概况,并将这些发现与从脑梗死患者获得的人脑标本进行了比较。通过双侧颈动脉闭塞联合低血压在常温成年大鼠中诱导短暂性前脑缺血(TFI)。在缺血后6、12、18、24、48和72小时以及7、14和28天处死动物(每个时间点n = 4)。使用光学和电子显微镜以及TUNEL组织化学分析实验组织。还使用光学显微镜和TUNEL组织化学检查了总共27个人脑标本,这些标本经神经病理学证实有缺血损伤并设有适当对照。实验性缺血后48和72小时,海马CA-1神经元出现密集的TUNEL染色。在这些时间之前,几乎没有或没有观察到核染色,而在72小时后核染色迅速减少。这些时间点的超微结构发现显示出许多与凋亡细胞中所见特征相似的特征,例如细胞收缩伴电子密度增加、染色质凝聚形成异染色质、完整的质膜和完整的细胞内细胞器。以类似的方式,亚急性期的人类中风标本在半暗带神经元中显示出密集的核TUNEL染色,而在急性期或慢性期几乎没有或没有观察到染色。我们的结果表明,人类中风后形态学变化和TUNEL组织化学的时间与实验性TFI中观察到的相似。此外,实验性缺血和人类中风中的神经元死亡都具有凋亡细胞死亡的几个特征。