Cho Injeong, Song Hyun-Ok, Cho Jeong Hoon
Department of Biology Education College of Education Chosun University Gwangju Korea.
Department of Infection Biology Wonkwang University School of Medicine Iksan Jeonbuk Korea.
Food Sci Nutr. 2020 Oct 23;8(12):6633-6642. doi: 10.1002/fsn3.1956. eCollection 2020 Dec.
Dietary supplementation of flavonoids has been shown to reduce the severity of neurodegenerative disorders such as dementia, Parkinson's disease, and Alzheimer's disease by their antioxidant effects. However, their low bioavailability raises the question of how much their antioxidant capacity actually contributes to the mitigating effects. The physicochemical properties of flavonoids suggest they could function as mitochondrial uncouplers. Moreover, mitochondrial uncoupling alleviated neurodegeneration in during aging in previous research. Therefore, we investigated whether various flavonoids (fisetin, quercetin, apigenin, chrysin, catechin, and naringenin) could reduce neuronal defects by mitochondrial uncoupling in . Both neuronal defects and mitochondrial membrane potential were reduced in aged worms in nearly all of the flavonoid treatments suggesting that flavonoids may reduce neurodegeneration in . However, there was no significant reduction of neuronal defects in mitophagy-deficient double mutants under flavonoid treatments. These results suggest that flavonoids could function as mitochondrial uncouplers to mitigate neurodegeneration in aged , possibly via a PINK1/Parkin mitophagy process.
饮食中补充类黄酮已被证明可通过其抗氧化作用减轻神经退行性疾病(如痴呆、帕金森病和阿尔茨海默病)的严重程度。然而,它们较低的生物利用度引发了一个问题,即它们的抗氧化能力实际上对减轻作用有多大贡献。类黄酮的物理化学性质表明它们可能作为线粒体解偶联剂发挥作用。此外,在先前的研究中,线粒体解偶联在衰老过程中减轻了神经退行性变。因此,我们研究了各种类黄酮(非瑟酮、槲皮素、芹菜素、白杨素、儿茶素和柚皮素)是否能通过线粒体解偶联减少[具体生物名称未给出]中的神经元缺陷。几乎所有类黄酮处理的衰老蠕虫中的神经元缺陷和线粒体膜电位均降低,这表明类黄酮可能减少[具体生物名称未给出]中的神经退行性变。然而,在类黄酮处理下,线粒体自噬缺陷的[具体生物名称未给出]双突变体中的神经元缺陷没有显著减少。这些结果表明,类黄酮可能作为线粒体解偶联剂,可能通过PINK1/Parkin线粒体自噬过程减轻衰老[具体生物名称未给出]中的神经退行性变。