Caro Pilar, Gómez José, Sánchez Inés, López-Torres Mónica, Barja Gustavo
Departamento de Fisiología Animal II, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, España.
Rev Esp Geriatr Gerontol. 2009 Jul-Aug;44(4):194-9. doi: 10.1016/j.regg.2009.01.003. Epub 2009 Jul 3.
Protein or methionine restriction in the diet is known to decrease reactive oxygen species (ROS) production and mitochondrial oxidative stress and to increase maximum longevity in rodents, which could explain how these changes also take place in dietary restriction. However, it is not known whether restriction of other amino acids is also involved. To clarify this question, we studied the effect of restricting all the amino acids, except methionine, of the semi-purified diet, AIN 93G, in Wistar rats.
Seven-week old male Wistar rats (n=16) were randomly divided into two groups: a control group and a group with 40% restriction of dietary amino acids except methionine. After 7 weeks of dietary treatment, the animals were sacrificed and their livers were extracted to isolate mitochondria immediately and measure ROS production and oxygen consumption; these data allowed the percentage of free radical leak to be calculated. Oxidative damage to mitochondrial DNA was calculated as 8-oxo-7,8-dihydro-2'-deoxyguanosine by HPLC-EC.
At the end of the experimental period, a decrease in kidney weight was observed, but the weight of the liver, heart and brain was unchanged. ROS production in isolated liver mitochondria was unchanged with complex I (pyruvate/malate or glutamate/malate) or complex II (succinate) linked substrates. Maximum rates of ROS production significantly decreased with glutamate/malate+rotenone but not with pyruvate/malate+rotenone or with succinate. There were no changes in oxygen consumption with any substrate either in state 4 (resting) or in state 3 (phosphorylating). In agreement with the ROS production results, there were no differences between groups in oxidative damage to mitochondrial DNA.
Taken together with previous results concerning methionine restriction, the results obtained in the present study clearly show that the decrease in ingestion of only one molecule, methionine, causes the decrease in ROS production and oxidative damage to mitochondrial DNA that is observed in dietary restriction in relation to the decrease in the rate of aging.
已知饮食中蛋白质或蛋氨酸限制可减少活性氧(ROS)生成及线粒体氧化应激,并延长啮齿动物的最大寿命,这或许能解释饮食限制中这些变化是如何发生的。然而,尚不清楚其他氨基酸的限制是否也有影响。为阐明这个问题,我们研究了在Wistar大鼠中限制半纯化饮食AIN 93G中除蛋氨酸外的所有氨基酸的效果。
将7周龄雄性Wistar大鼠(n = 16)随机分为两组:对照组和饮食中除蛋氨酸外氨基酸限制40%的组。经过7周饮食处理后,处死动物并立即取出肝脏以分离线粒体,测量ROS生成和氧气消耗;这些数据可用于计算自由基泄漏百分比。通过高效液相色谱 - 电化学法将线粒体DNA的氧化损伤计算为8 - 氧代 - 7,8 - 二氢 - 2'-脱氧鸟苷。
在实验期末,观察到肾脏重量下降,但肝脏、心脏和大脑重量未变。分离的肝线粒体中,与复合体I(丙酮酸/苹果酸或谷氨酸/苹果酸)或复合体II(琥珀酸)相关底物的ROS生成未变。谷氨酸/苹果酸 + 鱼藤酮时ROS生成的最大速率显著降低,但丙酮酸/苹果酸 + 鱼藤酮或琥珀酸时未降低。在状态4(静息)或状态3(磷酸化)下,任何底物的氧气消耗均无变化。与ROS生成结果一致,两组线粒体DNA的氧化损伤无差异。
结合先前关于蛋氨酸限制的结果,本研究获得的结果清楚表明,仅一种分子蛋氨酸摄入量的减少导致了饮食限制中观察到的ROS生成减少以及线粒体DNA的氧化损伤减少,这与衰老速率降低相关。