Abdel-Rahman A, Parks J K, Devereaux M W, Sokol R J, Parker W D, Rosenberg A A
Section of Neonatal Medicine, University of Colorado School of Medicine, Denver 80262, USA.
Proc Soc Exp Biol Med. 1995 Jun;209(2):170-7. doi: 10.3181/00379727-209-43892.
Previously, our laboratory has demonstrated inhibition of mitochondrial state 3 (ADP-dependent) respiration 5 min after resuscitation from an asphyxial insult in lambs less than 3 days of age. Older lambs were resistant to this transient mitochondrial dysfunction. This study was designed to examine if age-related differences in baseline state 3 mitochondrial respiration, electron transport chain activity, or susceptibility to oxygen free radical-mediated lipid peroxidation were related to the previously observed differences in postasphyxial mitochondrial respiration. Mitochondrial respiration was measured in 24 nonasphyxiated control lambs aged 1-10 days using four different substrates. Electron transport chain activity was assessed in 15 of these lambs, and lipid peroxidation measured as conjugated diene production was measured in 11 of these lambs. These lambs were all ventilated to maintain normal blood gases for a time period equal to the length of the hypoxic insult in asphyxiated lambs (see below), after which samples of brain were removed for isolation of mitochondria. A second group of 11 lambs (seven < or = 3 days of age and four > 3 days of age) were asphyxiated. The insult was a 75-to-90-min episode of hypoxia and hypercarbia that resulted in bradycardia and systemic hypotension over the final 15 min of the insult. At the end of asphyxia, the lambs were resuscitated and returned to control ventilator settings. Samples of brain were removed 5 min after resuscitation. Postasphyxia electron transport chain activity and lipid peroxidation were measured. All measurements described above were done in both nonsynaptic (primarily glial in origin) and synaptic mitochondria. State 3 mitochondrial respiration varied significantly with age, decreasing by an average of 41.2% +/- 11.1% (mean +/- SEM) from Day 2 to Day 5-6 and then increasing back to levels similar to Day 2 by Day 8-10 in nonsynaptic mitochondria. State 3 respiration in synaptic mitochondria decreased 60.6% +/- 5.2% from Day 2 to Day 5-6 before returning to levels similar to Day 2 by Day 8-10. Resting (nonADP-dependent) state 4 respiration demonstrated similar developmental patterns. Electron transport chain activities did not vary with age in the nonasphyxiated control animals. In addition, an asphyxial insult did not diminish electron transport chain activities in either lambs < or = 3 days old or those > 3 days of age.(ABSTRACT TRUNCATED AT 400 WORDS)
此前,我们的实验室已证明,出生不到3天的羔羊在窒息性损伤复苏后5分钟,其线粒体状态3(ADP依赖性)呼吸受到抑制。年龄较大的羔羊对这种短暂的线粒体功能障碍具有抗性。本研究旨在探讨基线状态3线粒体呼吸、电子传递链活性或对氧自由基介导的脂质过氧化的敏感性方面与年龄相关的差异,是否与先前观察到的窒息后线粒体呼吸差异有关。使用四种不同底物,对24只1 - 10日龄未窒息的对照羔羊的线粒体呼吸进行了测量。对其中15只羔羊评估了电子传递链活性,对其中11只羔羊测量了以共轭二烯生成量表示的脂质过氧化。这些羔羊均接受通气以维持正常血气,通气时间与窒息羔羊的缺氧损伤时长相等(见下文),之后取出脑样本以分离线粒体。第二组11只羔羊(7只≤3日龄,4只>3日龄)进行了窒息处理。损伤为75至90分钟的缺氧和高碳酸血症发作,在损伤的最后15分钟导致心动过缓和全身性低血压。窒息结束时,羔羊进行复苏并恢复到对照通气设置。复苏后5分钟取出脑样本。测量窒息后电子传递链活性和脂质过氧化。上述所有测量均在非突触(主要起源于神经胶质)和突触线粒体中进行。非突触线粒体中,状态3线粒体呼吸随年龄显著变化,从第2天到第5 - 6天平均下降41.2%±11.1%(平均值±标准误),然后到第8 - 10天回升至与第2天相似的水平。突触线粒体中状态3呼吸从第2天到第5 - 6天下降60.6%±5.2%,然后到第8 - 10天恢复到与第2天相似的水平。静息(非ADP依赖性)状态4呼吸呈现类似的发育模式。在未窒息的对照动物中,电子传递链活性不随年龄变化。此外,窒息性损伤并未降低≤3日龄或>3日龄羔羊的电子传递链活性。(摘要截断于400字)