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Protective Effect of Hwansodan in Serum and Glucose Deprivation Induced-apoptotic Death of PC12 Cells Via Ho-1 Expression  

Jung, Jae-Eun (Department of internal Medicine, School of Oriental Medicine)
Kim, Jin-Kyung (Department of Microbiology, School of Medicine, Wonkwang University)
Kang, Baek-Gyu (Department of internal Medicine, School of Oriental Medicine)
Park, Chan-Ny (Department of Microbiology, School of Medicine, Wonkwang University)
Park, Rae-Kil (Department of Microbiology, School of Medicine, Wonkwang University)
Moon, Byung-Soon (Department of internal Medicine, School of Oriental Medicine)
Publication Information
Journal of Physiology & Pathology in Korean Medicine / v.20, no.6, 2006 , pp. 1459-1466 More about this Journal
Abstract
The water extract of Hwansodan has been traditionally used for treatment of ischemic brain damage in oriental medicine. However, little is known about the mechanism by which the water extract of Hwansodan rescues cells from neurodegenerative disease. PC12 pheochromocytoma cells have been used extensively as a model for studying the cellular and molecular mechanisms of neuronal cell damages. Under deprivation of growth factor and ischemic injury, PC12 cells spontaneously undergoes apoptotic cell death. Serum and glucose deprivation markedly decreased the viability of PC12 cells, which was characterized with apparent apoptotic features such as membrane blebbing as well as fragmentation of genomic DNA and nuclei. However, the aqueous extract of Hwansodan significantly reduced serum and glucose deprivation-induced cell death and apoptotic characteristics through reduction of intracellular peroxide generation. Pretreatment of Hwansodan also ingibited the activation of caspase-3, in turn, degradation of ICAD/DFF45 was completely abolished in serum and glucose deprivated cells. Furthermore, pretreatment of Hwansodan obviously increased heme oxygenase 1 (HO-1) expression in PC12 cells. Taken together, the data suggest that the protective effects of Hwansodan against serum and glucose deprivation induced oxidative injuries may be achieved through the scavenging of reactive oxygene species accompanying with HO-1 induction.
Keywords
Hwansodan; HO-1; PC12; apoptosis; protective effect;
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