Department of Biological Sciences, KAIST (Korea Advanced Institute of Science and Technology), Daejeon, Korea.
PLoS One. 2012;7(10):e47122. doi: 10.1371/journal.pone.0047122. Epub 2012 Oct 11.
NADH-quinone oxidoreductase 1 (NQO1) modulates cellular NAD(+)/NADH ratio which has been associated with the aging and anti-aging mechanisms of calorie restriction (CR). Here, we demonstrate that the facilitation of NQO1 activity by feeding β-lapachone (βL), an exogenous NQO1 co-substrate, prevented age-dependent decline of motor and cognitive function in aged mice. βL-fed mice did not alter their food-intake or locomotor activity but did increase their energy expenditure as measured by oxygen consumption and heat generation. Mitochondrial structure and numbers were disorganized and decreased in the muscles of control diet group but those defects were less severe in βL-fed aged mice. Furthermore, for a subset of genes associated with energy metabolism, mice fed the βL-diet showed similar changes in gene expression to the CR group (fed 70% of the control diet). These results support the potentiation of NQO1 activity by a βL diet and could be an option for preventing age-related decline of muscle and brain functions.
烟酰胺腺嘌呤二核苷酸(NADH)-醌氧化还原酶 1(NQO1)调节细胞内 NAD(+)/NADH 比值,这与热量限制(CR)的衰老和抗衰老机制有关。在这里,我们证明通过喂食β-拉帕醌(βL),一种外源性 NQO1 辅酶,促进 NQO1 活性,可防止老年小鼠运动和认知功能的年龄依赖性下降。βL 喂养的小鼠不会改变它们的食物摄入量或运动活性,但会增加能量消耗,如通过耗氧量和产热量测量。在对照组的肌肉中,线粒体结构和数量紊乱且减少,但在βL 喂养的老年小鼠中,这些缺陷不那么严重。此外,对于与能量代谢相关的一组基因,喂食βL 饮食的小鼠表现出与 CR 组(喂食对照组的 70%)相似的基因表达变化。这些结果支持通过βL 饮食增强 NQO1 活性,并且可能是预防与年龄相关的肌肉和大脑功能下降的一种选择。