Suppr超能文献

[琥珀酸对大鼠肝线粒体诱导脂质过氧化作用的年龄相关性特点]

[Age-related Peculiarities of Succinate Effect on Induced Lipid Peroxidation in Rat Liver Mitochondria].

作者信息

Grishina E V, Khaustova Ya V, Vasilieva A A, Mayevsky E I

出版信息

Biofizika. 2015 Jul-Aug;60(4):708-15.

Abstract

The antioxidant effect of succinate and 3-hydroxybutyrate oxidation on the kinetics of lipid peroxidation induced by ATP-Fe2+ complex in isolated rat liver mitochondria of old (1.0-1.5 years) and young (3 months) male rats was investigated. The rate of induced lipid peroxidation V(LPO) in rat liver mitochondria and the half-time of oxygen consumption Δt50, which included the lag period and the initiation. phase, was recorded polarographically. Without exogenous oxidative-substrates V(LPO) was slightly higher in mitochondria of old animals, but the onset of lipid peroxidation cascade was significantly earlier than in young animals. Incubation of mitochondria with 5mM succinate for 1 min inhibited V(LPO) by 15% in young animals and by 35% in old animals. However, only in mitochondria of old animals Δt50 increased by 19% as compared to lipid peroxidation without substrates. V(LPO) in mitochondria of young animals did not significantly change during 3-hydroxybutyrate oxidation, while in mitochondria of old animals it was reduced by 19% with a slight increase in Δt50. To simulate age-dependent dysfunction we damaged isolated mitochondria by a series of freeze-thaw cycles, which caused a significant increase of V(LPO) of.both age groups. Succinate oxidation inhibited V(LPO) in damaged mitochondria in all cases by 56%, as compared to V(LPO) without oxidative substrates and extended At50 twofold in mitochondria of young animals. Oxidation of 3-hydroxybutyrate had no effect on V(LPO) in damaged mitochondria regardless of animal, age and extended Δt50 by 48% in mitochondria of young animals. Thus, the antioxidant effect of succinate oxidation can prevent lipid peroxidation damage and may exhibit geroprotective action at the level of aging mitochondria. Therefore, the antioxidant effect is due to the process of substrate oxidation in the respiratory chain but not because of an interaction of their structures with membrane lipids per se.

摘要

研究了琥珀酸和3-羟基丁酸氧化对老年(1.0 - 1.5岁)和幼年(3个月)雄性大鼠离体肝线粒体中ATP-Fe2+复合物诱导的脂质过氧化动力学的抗氧化作用。通过极谱法记录大鼠肝线粒体中诱导脂质过氧化的速率V(LPO)以及耗氧半衰期Δt50,其中包括延迟期和起始阶段。在没有外源性氧化底物的情况下,老年动物线粒体中的V(LPO)略高,但脂质过氧化级联反应的起始明显早于幼年动物。用5mM琥珀酸孵育线粒体1分钟,幼年动物中V(LPO)降低15%,老年动物中降低35%。然而,仅在老年动物的线粒体中,与无底物的脂质过氧化相比,Δt50增加了19%。在3-羟基丁酸氧化过程中,幼年动物线粒体中的V(LPO)没有显著变化,而老年动物线粒体中的V(LPO)降低了19%,同时Δt50略有增加。为了模拟年龄依赖性功能障碍,我们通过一系列冻融循环损伤离体线粒体,这导致两个年龄组的V(LPO)显著增加。与无氧化底物时的V(LPO)相比,琥珀酸氧化在所有情况下均抑制受损线粒体中的V(LPO)达56%,并使幼年动物线粒体中的At50延长两倍。无论动物年龄如何,3-羟基丁酸氧化对受损线粒体中的V(LPO)均无影响,且使幼年动物线粒体中的Δt50延长了48%。因此,琥珀酸氧化的抗氧化作用可以防止脂质过氧化损伤,并可能在衰老线粒体水平上发挥老年保护作用。因此,抗氧化作用是由于呼吸链中底物氧化过程,而不是因为它们的结构与膜脂质本身相互作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验