Ischemic intensity influences the distribution of delayed infarction and apoptotic cell death following transient focal cerebral ischemia in rats

• Published in: Brain research 2002-11, Vol.956 (1), p.14-23
• Main Authors: Lee, Seung-Hoon, Kim, Manho, Kim, Young-Ju, Kim, Young-A, Chi, Je-Geun, Roh, Jae-Kyu, Yoon, Byung-Woo
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Apoptosis - physiology; Benzimidazoles; Biological and medical sciences; Caspase 3; Caspases - metabolism; Cerebral Cortex - metabolism; Cerebral Cortex - pathology; Cerebral Cortex - ultrastructure; Focal cerebral ischemia; In Situ Nick-End Labeling; Ischemic Attack, Transient - metabolism; Ischemic Attack, Transient - pathology; Male; Medical sciences; Microscopy, Electron; Middle Cerebral Artery - pathology; Neurology; Rats; Rats, Sprague-Dawley; Regional distribution; Reperfusion; Staining and Labeling; Time Factors; Vascular diseases and vascular malformations of the nervous system
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/S0006-8993(02)03197-9

The aim of this study was to investigate whether the apoptotic process contributes to the delayed infarction that follows a middle cerebral artery (MCA) occlusion of 20 min (mild ischemia group) and to compare this with the delayed component of infarct following 2 h of MCA occlusion (severe ischemia group). Adult male Sprague–Dawley rats underwent left MCA occlusion for either 20 min or 2 h and were reperfused for 12, 24 and 72 h. On 2,3,5-triphenyltetrazolium chloride-stained coronal sections, delayed infarction was observed to develop in the whole MCA territory after mild ischemia, and also in the frontoparietal cortex after severe ischemia. At 24 h after 20 min of MCA occlusion, characteristic apoptotic features, including chromatin condensation and apoptotic bodies were frequently observed by electron microscopy. In both ischemic groups, Hoechst 33342 staining showed typically condensed and fragmented nuclei in the area showing delayed infarction, where TdT–dUTP nick end labeling (TUNEL)-positive cells were also significantly increased. Caspase-3 activity was also found to be elevated 24 and 72 h after reperfusion and this peaked at 24 h in both groups. These findings suggest that ischemic severity may influence the distribution of delayed infarction, and that apoptosis is the underlying pathophysiologic mechanism.