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Protective effect of Korean Red Ginseng against FK506-induced damage in LLC-PK1 cells

Authors
Lee, DahaeKang, Ki SungYu, Jae SikWoo, Jung-YoonHwang, Gwi SeoEom, Dae-WoonBaek, Seung-HoonLee, Hye LimKim, Ki HyunYamabe, Noriko
Issue Date
Jul-2017
Publisher
KOREAN SOC GINSENG
Keywords
FK506; Korean Red Ginseng; nephrotoxicity; MAPKs
Citation
JOURNAL OF GINSENG RESEARCH, v.41, no.3, pp.284 - 289
Journal Title
JOURNAL OF GINSENG RESEARCH
Volume
41
Number
3
Start Page
284
End Page
289
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/5981
DOI
10.1016/j.jgr.2016.05.002
ISSN
1226-8453
Abstract
Background: Compound FK506 is an immunosuppressant agent that is frequently used to prevent rejection of solid organs upon transplant. However, nephrotoxicity due to apoptosis and inflammatory response mediated by FK506 limit its usefulness. In this study, the protective effect of Korean Red Ginseng (KRG) against FK506-induced damage in LLC-PK1 pig kidney epithelial cells was investigated. Methods: LLC-PK1 cells were exposed to FK506 with KRG and cell viability was measured. Western blotting and RT-PCR analyses evaluated protein expression of MAPKs, caspase-3, and KIM-1. TLR-4 gene expression was assessed. Caspase-3 activities were also determined. The number of apoptotic cells was measured using an image-based cytometric assay. Results: The reduction in LLC-PK1 cell viability by 60 mu M FK506 was recovered by KRG cotreatment in a dose-dependent manner. The phosphorylation of p38, p44/ 42 MAPKs (ERK), KIM-1, cleaved caspase-3, and TLR-4 mRNA expression was increased markedly in LLC-PK1 cells treated with 60 mu M FK506. However, with the exception of p-ERK, elevated levels of p-p38, KIM-1, cleaved caspase-3, and TLR-4 mRNA expression were significantly decreased after cotreatment with KRG. Activity level of caspase-3 was also attenuated by KRG cotreatment. Moreover, image-based cytometric assay showed that apoptotic cell death was increased by 60 mu M FK506 treatment, whereas it was decreased after cotreatment with KRG. Conclusion: Taken together, these results suggest that the molecular mechanism of KRG in the FK506induced nephrotoxicity may lead to the development of an adjuvant for the inhibition of adverse effect FK506 in the kidney. (C) 2016 The Korean Society of Ginseng, Published by Elsevier Korea LLC.
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College of Korean Medicine (Premedical course of Oriental Medicine)
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