Structure-Activity Relationship Study of Vitamin K Derivatives Yields Highly Potent Neuroprotective Agents

被引:77
作者
Josey, Benjamin J. [1 ]
Inks, Elizabeth S. [1 ]
Wen, Xuejun [2 ]
Chou, C. James [1 ]
机构
[1] Med Univ S Carolina, S Carolina Coll Pharm, Dept Drug Discovery & Biomed Sci, Charleston, SC 29425 USA
[2] Virginia Commonwealth Univ, Dept Chem & Life Sci Engn, Richmond, VA 23284 USA
基金
美国国家卫生研究院;
关键词
OXIDATIVE GLUTAMATE TOXICITY; NEURONAL CELL-LINE; NEURODEGENERATIVE DISEASES; MITOCHONDRIAL FISSION; DEPENDENT PROTEINS; BRAIN-INJURY; IN-VITRO; STRESS; DEATH; MENAQUINONE-4;
D O I
10.1021/jm301485d
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Historically known for its role in blood coagulation and bone formation, vitamin K (VK) has begun to emerge as an important nutrient for brain function. While VK involvement in the brain has not been fully explored, it is well-known that oxidative stress plays a critical role in neuro-degenerative diseases. It was recently reported that VK protects neurons and oligodendrocytes from oxidative injury and rescues Drosophila from mitochondrial defects associated with Parkinson's disease. In this study, we take a chemical approach to define the optimal and minimum pharmacophore responsible for the neuroprotective effects of VK. In doing so, we have developed a series of potent VK analogues with favorable drug characteristics that provide full protection at nanomolar concentrations in a well-defined model of neuronal oxidative stress. Additionally, we have characterized key cellular responses and biomarkers consistent with the compounds' ability to rescue cells from oxidative stress induced cell death.
引用
收藏
页码:1007 / 1022
页数:16
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