Asymmetrical Dimethylarginine Antagonizes Glutamate-Induced Apoptosis in PC12 Cells

作者：Wang, Xiang-Yu^*; Zhao, Jing; Yang, Hong-Wei

来源：Journal of Molecular Neuroscience, 2013, 49(1): 89-95.

DOI：10.1007/s12031-012-9897-z

• Asymmetric dimethylarginine
• Apoptosis
• bcl-2
• Excitotoxicity
• Glutamate
• Nitric oxide

Overproduction of nitric oxide (NO) plays an important role in glutamate-induced excitotoxicity. Asymmetric dimethylarginine (ADMA) is an endogenous nitric oxide synthase (NOS) inhibitor. The aim of this study is to explore whether ADMA antagonizes the excitotoxicity of glutamate to neuronal cells and the underlying molecular mechanisms. In this work, we investigated the effects of ADMA on glutamate-induced toxicity in neuronal cells by studying PC12 cells, a clonal rat pheochromocytoma cell line. We show that ADMA obviously protects PC12 cells against glutamate-induced cytotoxicity and apoptosis. We also found that ADMA treatment results in prevention of glutamate-induced mitochondrial membrane potential loss and caspase-3 activation. Moreover, ADMA prevents glutamate-caused down-regulation of bcl-2 protein expression. These results indicate that ADMA protects against glutamate-induced apoptosis and excitotoxicity and the underlying mechanism may be involved in preservation of mitochondrial function by up-regulating the expression of bcl-2. Our study suggests a promising future of ADMA-based therapies for neuropathologies associated with an excess of NO.

• 出版日期2013-1
• 单位三峡大学; 南华大学