Oxidative stress in Niemann-Pick disease, type C

被引:98
作者
Fu, Rao [1 ,2 ]
Yanjanin, Nicole M. [1 ]
Bianconi, Simona [1 ]
Pavan, William J. [3 ]
Porter, Forbes D. [1 ]
机构
[1] NICHD, Program Dev Endocrinol & Genet, NIH, DHHS, Bethesda, MD 20892 USA
[2] Peking Univ, Hlth Sci Ctr, Beijing 100191, Peoples R China
[3] NHGRI, Genet Dis Res Branch, NIH, DHHS, Bethesda, MD 20892 USA
关键词
Neurodegenerative disease; Lysosomal storage disease; Oxidative stress; Coenzyme Q10; Trolox equivalent antioxidant capacity; LOW-DENSITY-LIPOPROTEIN; COENZYME Q(10); CHOLESTEROL HOMEOSTASIS; MITOCHONDRIAL-FUNCTION; ALZHEIMERS-DISEASE; ALPHA-TOCOPHEROL; BINDING PROTEIN; METABOLISM; GENE; ACCUMULATION;
D O I
10.1016/j.ymgme.2010.06.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Niemann-Pick disease, type C (NPC) is a neurodegenerative lysosomal storage disorder due to impaired intracellular cholesterol and lipid transport. Increased oxidative stress has been reported in human NPC1 mutant fibroblasts and in tissues from Npc1 mutant mice. However, oxidative stress in NPC patients has not been established. In this study, we demonstrated increased oxidative stress in NPC patients. Evaluation of serum from 37 NPC patients, compared to control values, showed significant decreases (p<.01) in both the fraction of reduced coenzyme Q10 (CoQ10) and trolox equivalent antioxidant capacity (TEAC). Both findings are consistent with increased oxidative stress in NPC. Supplementation with CoQ10 was not effective in correcting the decreased fraction of reduced CoQ10. Increased oxidative stress may be a contributing factor to the pathology of NPC, and demonstration of increased oxidative stress in NPC patients provides both a rationale and the biomarkers necessary to test the efficacy of antioxidant therapy in NPC. Published by Elsevier Inc.
引用
收藏
页码:214 / 218
页数:5
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