β-Guanidinopropionic Acid Stimulates Brain Mitochondria Biogenesis and Alters Cognitive Behavior in Nondiseased Mid-Age Mice.

Journal of Experimental Neuroscience Pub Date : 2018-04-02 eCollection Date: 2018-01-01 DOI:10.1177/1179069518766524
Artem P Gureev, Ekaterina A Shaforostova, Anatoly A Starkov, Vasily N Popov
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引用次数: 9

Abstract

β-guanidinopropionic acid (β-GPA) has been used as a nutritional supplement for increasing physical strength and endurance with positive and predictable results. In muscles, it works as a nonadaptive stimulator of mitochondria biogenesis; it also increases lipid metabolism. There are data indicating that β-GPA can be also neuroprotective, but its mechanisms of action in the brain are less understood. We studied the effects of β-GPA on animal behavior and mitochondrial biogenesis in the cortex and midbrain of mid-age healthy mice. We found that even short-term 3-week-long β-GPA treatment increased the mitochondrial DNA (mtDNA) copy number in the cortex and ventral midbrain, as well as the expression of several key antioxidant and metabolic enzymes-indicators of mitochondria proliferation and the activation of Nrf2/ARE signaling cascade. At the same time, β-GPA downregulated the expression of the β-oxidation genes. Administration of β-GPA in mice for 3 weeks improved the animals' physical strength and endurance health, ie, increased their physical strength and endurance and alleviated anxiety. Thus, β-GPA might be considered an adaptogene affecting both the muscle and brain metabolism in mammals.

Abstract Image

Abstract Image

Abstract Image

β-胍丙酸刺激未患病中年小鼠脑线粒体生物发生并改变认知行为
β-胍丙酸(β-GPA)已被用作一种营养补充剂,以增加体力和耐力,积极和可预测的结果。在肌肉中,它是线粒体生物生成的非适应性刺激物;它还能增加脂质代谢。有数据表明,β-GPA也可以起到神经保护作用,但其在大脑中的作用机制尚不清楚。我们研究了β-GPA对中年健康小鼠皮质和中脑动物行为和线粒体生物发生的影响。我们发现,即使是3周的短期β-GPA处理也增加了线粒体DNA (mtDNA)在皮层和中脑腹侧的拷贝数,以及线粒体增殖和Nrf2/ARE信号级联激活的几种关键抗氧化和代谢酶的表达。同时,β-GPA下调β-氧化基因的表达。β-GPA给药3周后,小鼠的体力和耐力健康得到改善,即增强了小鼠的体力和耐力,减轻了小鼠的焦虑。因此,β-GPA可能被认为是一种影响哺乳动物肌肉和脑代谢的适应基因。
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