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http://dx.doi.org/10.4062/biomolther.2011.19.2.195

Cytoprotective Effects of Docosyl Cafferate against tBHP-Induced Oxidative Stress in SH-SY5Y Human Neuroblastoma Cells  

Choi, Yong-Jun (Department of Pharmacology, College of Medicine, Kangwon National University)
Kwak, Eun-Bee (Department of Pharmacology, College of Medicine, Kangwon National University)
Lee, Jae-Won (Department of Pharmacology, College of Medicine, Kangwon National University)
Lee, Yong-Suk (Department of Anesthesiology, College of Medicine, Kangwon National University)
Cheong, Il-Young (Department of Anesthesiology, College of Medicine, Kangwon National University)
Lee, Hee-Jae (Department of Pharmacology, College of Medicine, Kangwon National University)
Kim, Sung-Soo (Department of Pharmacology, College of Medicine, Kangwon National University)
Kim, Myong-Jo (Division of Bio-resources Technology, Kangwon National University)
Kwon, Yong-Soo (College of Pharmacy, Kangwon National University)
Chun, Wan-Joo (Department of Pharmacology, College of Medicine, Kangwon National University)
Publication Information
Biomolecules & Therapeutics / v.19, no.2, 2011 , pp. 195-200 More about this Journal
Abstract
Neuronal cell death is a common characteristic feature of a variety of neurodegenerative disorders including Alzheimer's disease and Parkinson's disease. However, there have been no effective drugs to successfully prevent neuronal death in those diseases. In the present study, docosyl cafferate (DC), a derivative of caffeic acid, was isolated from Rhus verniciflua and its protective effects on tBHP-induced neuronal cell death were examined in SH-SY5Y human neuroblastoma cells. Pretreatment of DC significantly attenuated tBHP-induced neuronal cell death in a concentration-dependent manner. DC also significantly suppressed tBHP-induced caspase-3 activation. In addition, DC restored tBHP-induced depletion of intracellular Bcl-2, an anti-apoptotic member of the Bcl-2 family. Furthermore, DC significantly suppressed tBHP-induced degradation of IKB, which retains $NF-{\kappa}B$ in the cytoplasm, resulting in the suppression of nuclear translocation of $NF-{\kappa}B$ and its subsequent activation. Taken together, the results clearly demonstrate that DC exerts its neuroprotective activity against tBHP-induced oxidative stress through the suppression of nuclear translocation of $NF-{\kappa}B$.
Keywords
Docosyl cafferate (DC); SH-SY5Y human neuroblastoma cells; tBHP; Apoptosis; $NF-{\kappa}B$;
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Times Cited By KSCI : 4  (Citation Analysis)
Times Cited By Web Of Science : 1  (Related Records In Web of Science)
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