Wojewoda Marta, Duszyński Jerzy, Szczepanowska Joanna
Nencki Institute of Experimental Biology, Department of Biochemistry, Pasteura 3, 02-093 Warsaw, Poland.
Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):890-6. doi: 10.1016/j.bbabio.2010.01.035. Epub 2010 Feb 4.
Mitochondrial diseases originate from mutations in mitochondrial or nuclear genes encoding for mitochondrial proteome. Neurogenic muscle weakness, ataxia and retinitis pigmentosa (NARP) syndrome is associated with the T8993G transversion in ATP6 gene which results in substitution at the very conservative site in the subunit 6 of mitochondrial ATP synthase. Defects in the mitochondrial respiratory chain and the ATPase are considered to be accompanied by changes in the generation of reactive oxygen species (ROS). This study aimed to elucidate effects of selenium on ROS and antioxidant system of NARP cybrid cells with 98% of T8993G mutation load. We found that selenium decreased ROS generation and increased the level and activity of antioxidant enzymes such as glutathione peroxidase (GPx) and thioredoxin reductase (TrxR). Therefore, we propose selenium to be a promising therapeutic agent not only in the case of NARP syndrome but also other diseases associated with mitochondrial dysfunctions and oxidative stress.
线粒体疾病源于编码线粒体蛋白质组的线粒体或核基因中的突变。神经源性肌肉无力、共济失调和色素性视网膜炎(NARP)综合征与ATP6基因中的T8993G颠换有关,该颠换导致线粒体ATP合酶亚基6中非常保守的位点发生替代。线粒体呼吸链和ATP酶的缺陷被认为伴随着活性氧(ROS)生成的变化。本研究旨在阐明硒对T8993G突变负荷为98%的NARP杂交细胞中ROS和抗氧化系统的影响。我们发现硒减少了ROS的生成,并提高了抗氧化酶如谷胱甘肽过氧化物酶(GPx)和硫氧还蛋白还原酶(TrxR)的水平和活性。因此,我们认为硒不仅在NARP综合征的治疗中,而且在其他与线粒体功能障碍和氧化应激相关的疾病中都是一种有前景的治疗药物。