Abe K, Kawagoe J, Kogure K
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Neurosci Lett. 1993 Apr 30;153(2):173-6. doi: 10.1016/0304-3940(93)90315-c.
The level of mRNA for cytochrome c oxidase subunit I (COX-I), which is encoded by mitochondrial DNA (mtDNA), progressively decreased in the hippocampal CA1 neurons of gerbils from 1-3 h of the reperfusion after 3.5 min of transient forebrain ischemia, and completely disappeared at 7 days. The activity of cytochrome c oxidase (COX) protein also showed the early decrease in the CA1 cells, and was followed by the reduction of the level of COX-I DNA after 2 days. However, the activity of succinic dehydrogenase (SDH), a mitochondrial enzyme that is encoded by nuclear DNA, maintained normal activity until 1 day in the CA1 cells, and significantly decreased at 7 days. These results suggest that the early onset and the progressive disturbance of a mitochondrial DNA expression found selectively in the CA1 neurons could cause progressive failure of energy production of the cells that eventually results in the neuronal cell death.
细胞色素c氧化酶亚基I(COX-I)的mRNA水平由线粒体DNA(mtDNA)编码,在短暂性前脑缺血3.5分钟后再灌注1至3小时的沙鼠海马CA1神经元中逐渐降低,并在7天时完全消失。细胞色素c氧化酶(COX)蛋白的活性在CA1细胞中也显示出早期降低,随后在2天后COX-I DNA水平降低。然而,琥珀酸脱氢酶(SDH)是一种由核DNA编码的线粒体酶,其活性在CA1细胞中直到1天都保持正常,在7天时显著降低。这些结果表明,选择性地在CA1神经元中发现的线粒体DNA表达的早期发生和进行性紊乱可能导致细胞能量产生的进行性衰竭,最终导致神经元细胞死亡。