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Cited 3 time in webofscience Cited 3 time in scopus
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Antioxidative mechanisms of sea buckthorn fruit extract in mouse embryonic fibroblast cells

Authors
Lim, Sae-RomGo, Eun-BiGo, GeonShin, Han-SeungSung, Jung-Suk
Issue Date
Feb-2013
Publisher
KOREAN SOCIETY FOOD SCIENCE & TECHNOLOGY-KOSFOST
Keywords
sea buckthorn fruit; oxidative stress; antioxidant activity; cell cycle; apoptosis
Citation
FOOD SCIENCE AND BIOTECHNOLOGY, v.22, no.1, pp 197 - 204
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
FOOD SCIENCE AND BIOTECHNOLOGY
Volume
22
Number
1
Start Page
197
End Page
204
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15334
DOI
10.1007/s10068-013-0067-z
ISSN
1226-7708
2092-6456
Abstract
This study was conducted to define the antioxidant properties and cytoprotective mechanisms of sea buckthorn fruit extract (SFE) against cellular oxidative stress in mouse embryonic fibroblast (MEF) cells. Cell viability of MEF cells damaged by H2O2 was significantly increased by addition of SFE in a concentration dependent manner. Cytoprotective effect of SFE against oxidative damage was observed to be co-related with regulation of cell cycle progression. Induction of cell cycle arrest in G(2)/ M checkpoint was mediated by oxidative stress, but significantly reduced by treatment of MEF cells with SFE. Analysis of key regulatory proteins involved in G(2)/M arrest showed that SFE treatment leads to down-regulation of both phosphorylated Chk1 and cyclin B, which play important roles in cell cycle arrest of oxidatively damaged cells. Effect of SFE on apoptosis was evaluated by morphological and flow cytometric analysis. Apoptotic cell accumulation occurred by H2O2 treatment was decreased by co-treatment of MEF cells with SFE. Early apoptotic process involved in DNA fragmentation and condensation was also inhibited by additional treatment with SFE. Overall results suggest that cytoprotective effect of SFE is mediated by effective radical scavenging activity as well as altered cell cycle regulation which prevent apoptotic cell death induced by cellular oxidative stress.
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