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大鼠脑突触体中过氧化氢生成及生物能量学的年龄相关变化。

Age-related changes in H2O2 production and bioenergetics in rat brain synaptosomes.

作者信息

Kilbride Seán M, Telford Jayne E, Davey Gavin P

机构信息

School of Biochemistry and Immunology and Trinity College Institute of Neuroscience, Trinity College Dublin, Ireland.

出版信息

Biochim Biophys Acta. 2008 Jul-Aug;1777(7-8):783-8. doi: 10.1016/j.bbabio.2008.05.445. Epub 2008 Jun 2.

Abstract

Detrimental changes to mitochondrial function have been shown to occur with age. In this study we examined the levels of H(2)O(2) production, in situ mitochondrial membrane potential (Deltapsi(m)), oxygen consumption (JO(2)) and electron transport chain (ETC) enzyme activities in synaptosomes isolated from rats of two age groups, 6 and 18 months. The rate of H(2)O(2) production in synaptosomes was found to be higher in the 18-month old group compared to that of 6-month old. Deltapsi(m) was found to be significantly lower in synaptosomes from the older rats, which also correlated with a reduction in JO(2). Measurement of the individual electron transport chain enzyme activities revealed that reduced complex II/III and complex IV activities were the possible contributors to the reduced bioenergetic function in synaptosomes from the older rats. These data suggest that ageing may lead to increased nerve terminal H(2)O(2) production while simultaneous deleterious effects on bioenergetic function occur in in situ synaptosomal mitochondria. In addition, Ca(2+)-independent glutamate release was found to be increased at lower levels of complex I inhibition in the synaptosomes from older rats, suggesting that reduction of mitochondrial function may potentiate excitotoxic conditions in the ageing brain.

摘要

线粒体功能的有害变化已被证明会随着年龄的增长而发生。在本研究中,我们检测了从6个月和18个月两个年龄组的大鼠分离出的突触体中H₂O₂的产生水平、原位线粒体膜电位(Δψm)、氧消耗(JO₂)以及电子传递链(ETC)酶活性。结果发现,18月龄组突触体中H₂O₂的产生速率高于6月龄组。老年大鼠突触体中的Δψm显著降低,这也与JO₂的降低相关。对各个电子传递链酶活性的测量表明,复合物II/III和复合物IV活性降低可能是老年大鼠突触体生物能量功能降低的原因。这些数据表明,衰老可能导致神经末梢H₂O₂产生增加,同时原位突触体线粒体的生物能量功能会受到有害影响。此外,发现老年大鼠突触体中在较低水平的复合物I抑制下,不依赖Ca²⁺的谷氨酸释放增加,这表明线粒体功能的降低可能会增强衰老大脑中的兴奋性毒性状况。

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