Protective Effect of Nervonic Acid Against 6-Hydroxydopamine-Induced Oxidative Stress in PC-12 Cells

被引:27
|
作者
Umemoto, Hiroki [1 ]
Yasugi, Saika [2 ]
Tsuda, Shinji [1 ]
Yoda, Minoru [1 ]
Ishiguro, Takashi [1 ]
Kaba, Naoko [2 ]
Itoh, Tatsuki [2 ]
机构
[1] Miyoshi Oil & Fat Co Ltd, Tech Dept, Div Foods, Katsushika Ku, 4-66-1 Horikiri, Tokyo 1248510, Japan
[2] Kindai Univ, Dept Food Sci & Nutr, Fac Agr, 3327-204 Nakamachi, Nara, Nara 6318505, Japan
关键词
nervonic acid; oxidative stress; PC-12; cell; Parkinson's disease; antioxidant; PREMATURE-INFANTS; GENE-EXPRESSION; FATTY-ACID; BRAIN; SPHINGOMYELIN; ELOVL1; C24;
D O I
10.5650/jos.ess20262
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Increased oxidative stress in the human brain is observed in neurodegenerative diseases such as Parkinson's disease (PD) and Alzheimer's disease (AD), and is considered to be a major cause of progression of these disease states. A very long-chain fatty acid, nervonic acid (NA), is the main fatty acid found in various sphingolipid species in the central nervous system. NA plays an important role in forming the plasma membrane's lipid bilayer and in maintaining normal myelin function. In this study, we examined the neuroprotective effect of NA against rat pheochromocytoma (PC-12) cells stimulated by 6-hydroxydopamine (6-OHDA), which served as a cell model of PD. PC-12 cells were pre-treated with different concentrations of NA for 48 h then subsequently co-treated with NA and 6-OHDA for 48 h to induce cellular oxidative stress. Cell viability was significantly increased by pre-treatment with a very low concentration of NA. The level of malondialdehyde, a marker of lipid peroxidation, was significantly decreased in NA-treated cells. The expression levels of superoxide dismutases (Mn SOD and Cu/Zn SOD) and gamma-glutamylcysteine synthetase (GCLC), responsible for the synthesis of glutathione, were significantly increased, indicating that pre-treatment with NA activated the cellular antioxidant defense system. These results suggest that NA may play a role as a neuroprotective mediator in the brain.
引用
收藏
页码:95 / 102
页数:8
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