DNA damage and repair in human spinal cord following ischemia–reperfusion injury

Glen Roseborough , Ruxian Lin , Daqing Gao, Amy McHale, Lei Chen, G. Melville Williams, Chiming Wei
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Abstract

Spinal cord ischemia leading to paraplegia is a rare, sporadic, but devastating complication of surgery on the thoracoabdominal aorta. Our patient, a 69-year-old man, succumbed from a stroke on the third hospital day following surgical repair. He also had bilateral leg paralysis. At autopsy done 4 h after death there were remarkable differences between the thoracic or normally perfused spinal cord and the lumbar potentially ischemia or reperfused spinal cord. The measurements of injury were small in the thoracic spinal cord and extensive in the lumbar spinal cord DNA D/R. Apoptotic cell numbers and apoptosis-related enzymes such as caspase-3 were increased in the lumbar spinal cord. These findings duplicated those we reported in the rabbit subjected to 30 min of aortic occlusion and reperfusion injury. This is the first report in humans documenting DNA oxidative injury and apoptosis in ischemia–reperfusion injury of the spinal cord.

人脊髓缺血再灌注损伤后DNA损伤与修复
脊髓缺血导致截瘫是胸腹主动脉手术中一种罕见、偶发但具有破坏性的并发症。我们的患者是一名69岁的男子,在手术修复后的第三天住院时死于中风。他还患有双侧腿部瘫痪。在死亡后4小时进行的尸检中,胸椎或正常灌注的脊髓与腰椎潜在缺血或再灌注的脊髓之间存在显著差异。损伤的测量在胸脊髓中很小,在腰脊髓DNA D/R中很广泛。腰髓中凋亡细胞数量和凋亡相关酶如胱天蛋白酶-3增加。这些发现与我们在遭受30分钟主动脉闭塞和再灌注损伤的兔子中报道的结果重复。这是人类首次记录脊髓缺血再灌注损伤中DNA氧化损伤和细胞凋亡的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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