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Age-related oxidative decline of mitochondrial functions in rat brain is prevented by long term oral antioxidant supplementation

机译:长期口服抗氧化剂可预防大鼠脑线粒体功能与年龄相关的氧化性下降

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摘要

A combination of antioxidants (N-acetyl cysteine, α-lipoic acid, and α-tocopherol) was selected for long term oral supplementation study in rats for protective effects on age-related mitochondrial alterations in the brain. Four groups of rats were chosen: young control (6-7 months); aged rats (22-24 months); aged rats (22-24 months) on daily antioxidant supplementation from 18 month onwards and young rats (6-7 months) on daily antioxidant supplementation from 2 month onwards. The brain mitochondrial functional parameters, status of antioxidant enzymes and accumulation of oxidative damage markers were measured in the four groups of rats. A significant decrease in complex IV activity and a loss of transmembrane potential and phosphorylation capacity along with an increased accumulation of oxidative damage markers and compromised antioxidant enzyme status were noticed in aged rat brain mitochondria as compared to that in young controls, but in aged rats supplemented with oral antioxidants the mitochondrial alterations were largely prevented. Antioxidant supplementation in young rats had no effect on mitochondrial parameters investigated in this study. The results have implications in biochemical and functional deficits of brain during aging as well as in neurodegenerative disorders.
机译:选择抗氧化剂的组合(N-乙酰半胱氨酸,α-硫辛酸和α-生育酚)用于大鼠的长期口服补充研究,以保护与年龄相关的脑线粒体改变。选择四组大鼠:年轻对照组(6-7个月);年轻组(6-7个月)。老年大鼠(22-24个月);从18个月起每天补充抗氧化剂的成年大鼠(22-24个月)和从2个月起每天补充抗氧化剂的年轻大鼠(6-7个月)。在四组大鼠中测量了脑线粒体功能参数,抗氧化酶的状态和氧化损伤标记物的积累。与年轻对照组相比,老年大鼠脑线粒体的复合物IV活性显着降低,跨膜电位和磷酸化能力的丧失,以及氧化损伤标记物的积累增加和抗氧化酶状态受损,但在补充了老年大鼠的脑线粒体中口服抗氧化剂可以大大防止线粒体改变。在年轻大鼠中补充抗氧化剂对本研究中研究的线粒体参数没有影响。该结果对衰老过程中大脑的生化和功能缺陷以及神经退行性疾病有影响。

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