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神经退行性疾病中的核黄素反应性线粒体功能障碍

Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases.

作者信息

Udhayabanu Tamilarasan, Manole Andreea, Rajeshwari Mohan, Varalakshmi Perumal, Houlden Henry, Ashokkumar Balasubramaniem

机构信息

Department of Genetic Engineering, School of Biotechnology, Madurai Kamaraj University, Madurai 625021, India.

Department of Molecular Neuroscience and Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.

出版信息

J Clin Med. 2017 May 5;6(5):52. doi: 10.3390/jcm6050052.

Abstract

Mitochondria are the repository for various metabolites involved in diverse energy-generating processes, like the TCA cycle, oxidative phosphorylation, and metabolism of amino acids, fatty acids, and nucleotides, which rely significantly on flavoenzymes, such as oxidases, reductases, and dehydrogenases. Flavoenzymes are functionally dependent on biologically active flavin adenine dinucleotide (FAD) or flavin mononucleotide (FMN), which are derived from the dietary component riboflavin, a water soluble vitamin. Riboflavin regulates the structure and function of flavoenzymes through its cofactors FMN and FAD and, thus, protects the cells from oxidative stress and apoptosis. Hence, it is not surprising that any disturbance in riboflavin metabolism and absorption of this vitamin may have consequences on cellular FAD and FMN levels, resulting in mitochondrial dysfunction by reduced energy levels, leading to riboflavin associated disorders, like cataracts, neurodegenerative and cardiovascular diseases, etc. Furthermore, mutations in either nuclear or mitochondrial DNA encoding for flavoenzymes and flavin transporters significantly contribute to the development of various neurological disorders. Moreover, recent studies have evidenced that riboflavin supplementation remarkably improved the clinical symptoms, as well as the biochemical abnormalities, in patients with neuronopathies, like Brown-Vialetto-Van-Laere syndrome (BVVLS) and Fazio-Londe disease. This review presents an updated outlook on the cellular and molecular mechanisms of neurodegenerative disorders in which riboflavin deficiency leads to dysfunction in mitochondrial energy metabolism, and also highlights the significance of riboflavin supplementation in aforementioned disease conditions. Thus, the outcome of this critical assessment may exemplify a new avenue to enhance the understanding of possible mechanisms in the progression of neurodegenerative diseases and may provide new rational approaches of disease surveillance and treatment.

摘要

线粒体是参与各种能量生成过程的多种代谢物的储存库,如三羧酸循环、氧化磷酸化以及氨基酸、脂肪酸和核苷酸的代谢,这些过程在很大程度上依赖于黄素酶,如氧化酶、还原酶和脱氢酶。黄素酶在功能上依赖于具有生物活性的黄素腺嘌呤二核苷酸(FAD)或黄素单核苷酸(FMN),它们来源于饮食成分核黄素,一种水溶性维生素。核黄素通过其辅因子FMN和FAD调节黄素酶的结构和功能,从而保护细胞免受氧化应激和凋亡。因此,核黄素代谢和这种维生素吸收的任何紊乱可能会影响细胞内FAD和FMN水平,导致能量水平降低从而引起线粒体功能障碍,进而导致与核黄素相关的疾病,如白内障、神经退行性疾病和心血管疾病等,这并不奇怪。此外,编码黄素酶和黄素转运蛋白的核DNA或线粒体DNA中的突变显著促成了各种神经系统疾病的发生。而且,最近的研究证明,核黄素补充剂能显著改善患有神经病的患者的临床症状以及生化异常,如布朗 - 维阿莱托 - 范 - 莱尔综合征(BVVLS)和法齐奥 - 隆德病。本综述介绍了神经退行性疾病的细胞和分子机制的最新观点,其中核黄素缺乏导致线粒体能量代谢功能障碍,并强调了核黄素补充剂在上述疾病状况中的重要性。因此,这一关键评估的结果可能为加深对神经退行性疾病进展中可能机制的理解开辟一条新途径,并可能为疾病监测和治疗提供新的合理方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c979/5447943/50df27c55cb8/jcm-06-00052-g001.jpg

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