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Protective Effect of Hypoxic Preconditioning on Hypoxic-Ischemic Injured Newborn Rats

机译:缺氧预处理对缺氧缺血性新生大鼠的保护作用

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摘要

Brief episodes of cerebral hypoxia-ischemia cause transient ischemic tolerance to subsequent ischemic events that are otherwise lethal. This study was conducted to evaluate the protective effect of hypoxic preconditioning on hypoxic-ischemic injury in the neonatal rat and the persistence of a protective window after hypoxic preconditioning. The rats were preconditioned with hypoxia (8% oxygen, 92% nitrogen) for three hours, subjected to ischemia using ligation of the right common carotid artery, and then exposed to another three hours of hypoxia. Using proton magnetic resonance spectroscopy, terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling (TUNEL) staining, and morphologic scores, this study shows that hypoxic preconditioning 6-hr to 1-day before hypoxic-ischemic injury increases survival rates and has neuroprotective effects against subsequent hypoxic-ischemic injury. The mechanism of the protective effects of hypoxic preconditioning in the newborn rat brain may involve downregulation of apoptotic cell death.
机译:脑缺氧缺血的短暂发作引起对随后的局部缺血事件的短暂的局部缺血耐受,否则这些局部缺血事件是致命的。进行这项研究以评估缺氧预处理对新生大鼠缺氧缺血性损伤的保护作用以及缺氧预处理后保护窗的持久性。用低氧(8%的氧气,92%的氮气)预处理大鼠3个小时,使用右颈总动脉结扎进行缺血,然后再暴露3个小时的缺氧。使用质子磁共振波谱,末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记(TUNEL)染色和形态学评分,该研究表明在缺氧缺血性损伤之前6小时至1天进行缺氧预处理可以提高生存率,并且对随后的缺氧缺血性损伤的神经保护作用。缺氧预处理对新生大鼠脑的保护作用机制可能涉及凋亡细胞死亡的下调。

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