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Cited 34 time in webofscience Cited 44 time in scopus
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Eucommia ulmoides Oliv. Bark. protects against hydrogen peroxide-induced neuronal cell death in SH-SY5Y cells

Authors
Kwon, Seung-HwanKim, Min-JungMa, Shi-XunYou, In-JeeHwang, Ji-YoungOh, Ji-HwanKim, Sun-YeouKim, Hyoung-ChunLee, Seok-YongJang, Choon-Gon
Issue Date
13-Jul-2012
Publisher
ELSEVIER IRELAND LTD
Keywords
Eucommia ulmoides Oliv. Bark; Hydrogen peroxide; Neuronal cell death; Neurodegenerative diseases; Alzheimer' s disease
Citation
JOURNAL OF ETHNOPHARMACOLOGY, v.142, no.2, pp.337 - 345
Journal Title
JOURNAL OF ETHNOPHARMACOLOGY
Volume
142
Number
2
Start Page
337
End Page
345
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16280
DOI
10.1016/j.jep.2012.04.010
ISSN
0378-8741
Abstract
Ethnopharmacological relevance: Eucommia ulmoides Oliv. Bark. (EUE), has commonly been used to fortify the muscles and lungs, lower blood pressure, prevent miscarriage, improve the tone of liver and kidneys, and promote longevity the traditional tonic medicines of Korea, China, and Japan. Aim of the study: In this study, we investigated that the neuroprotective activities and possible mechanisms of EUE aqueous extract in hydrogen peroxide (H2O2)-induced neuronal cell death in human SH-SY5Y neuroblastoma cells. Material and method: We examined the effects of EUE against H2O2-induced cytotoxicity, DNA condensation, the production of reactive oxygen species (ROS), loss of mitochondria membrane potential (MMP), the proteolysis of cleaved poly-ADP-ribose polymerase (PARP), and the expression of Bcl-2, Bcl-xL, cleaved caspase-3, and release of cytochrome c. Moreover, we attempted to determine whether EUE suppressed the phosphorylation of c-Jun N-terminal kinase (JNK), p38 mitogen-activated protein kinase (MAPK), extracellular signal-regulated kinase 1/2 (ERK 1/2), and phosphoinositide 3-kinase (PI3K)/Akt. Results: Pretreatment with EUE increased cell viability and inhibited cytotoxicity and DNA condensation. EUE also attenuated the increase in ROS production and MMP reduction. Western blot data revealed that EUE inhibited H2O2-induced up- or down-regulation of cleaved PARP, cleaved caspase-3, Bcl-2, and Bcl-xL. The EUE inhibited release of cytochrome c from mitochondria to the cytosol, and significantly attenuated H2O2-induced phosphorylation of JNK, p38 MAPK, ERK 1/2, and PI3K/Akt. Conclusion: The potent neuroprotective capacity of EUE, shown in these experiments. may potentially be applied in the prevention or treatment of neurodegenerative diseases such as Alzheimer's disease (AD). (C) 2012 Elsevier Ireland Ltd. All rights reserved.
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