Hypoxia affects the physiological behavior of rat cortical synaptosomes

被引:7
作者
Aldinucci, Carlo
Carretta, Alessandra
Ciccoli, Lucia
Leoncini, Silvia
Signorini, Cinzia
Buonocore, Giuseppe
Pessina, Gian Paolo [1 ]
机构
[1] Univ Siena, Dept Physiol, I-53100 Siena, Italy
[2] Univ Siena, Dept Pathophysiol Expt Med & Publ Hlth, I-53100 Siena, Italy
[3] Univ Siena, Dept Pediat Obstet & Reprod Med, Siena, Italy
关键词
mitochondrial respiration; mitochondrial membrane potential; lipid peroxidation; free iron release; F2-isoprostanes; free radicals;
D O I
10.1016/j.freeradbiomed.2007.03.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nerve cells, especially synaptosomes, are very susceptible to hypoxia and the subsequent oxidative stress. In this paper, we examined the effects of hypoxia (93% N-2:2% O-2:5% CO2, V/V/V) on rat cortical synaptosomes by evaluating modifications of synaptosomal mitochondrial respiration rate and ATP production, membrane potential, intrasynaptosomal mitochondrial Ca2+ concentration ([Ca2+](i)), and desferoxaminechelatable free iron and esterified F2-isoprostane levels after different periods of hypoxia and after 30 min of reoxygenation. Oxygen consumption decreased significantly during 120 min of hypoxia and was restored after reoxygenation. At the same time, ATP production decreased and remained significantly lower even after reoxygenation. This involved a depolarization of the synaptosomal mitochondrial membrane, although the [Ca2+](i) remained practically unchanged. Indeed, iron and F2-isoprostane levels, representing useful prediction markers for neurodevelopmental outcome, increased significantly after hypoxia, and there was a strong correlation between the two variables. On the whole our results indicate that synaptosomal mitochondria undergo mitoptosis after 2 h of hypoxia. (c) 2007 Published by Elsevier Inc.
引用
收藏
页码:1749 / 1756
页数:8
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