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Protective effect of Korean Red Ginseng against FK506-induced damage in LLC-PK1 cells
被引:10
|作者:
Lee, Dahae
[1
]
Kang, Ki Sung
[2
]
Yu, Jae Sik
[1
]
Woo, Jung-Yoon
[3
]
Hwang, Gwi Seo
[2
]
Eom, Dae-Woon
[4
]
Baek, Seung-Hoon
[5
]
Lee, Hye Lim
[2
]
Kim, Ki Hyun
[1
]
Yamabe, Noriko
[2
]
机构:
[1] Sungkyunkwan Univ, Sch Pharm, 2066 Seobu Ro, Suwon 16419, South Korea
[2] Gachon Univ, Coll Korean Med, 1342 Seongnamdaero, Seongnam 13120, South Korea
[3] Korea Ginseng Corp, Korea Ginseng Res Inst, Daejeon, South Korea
[4] Univ Ulsan, Gangneung Asan Hosp, Dept Pathol, Coll Med, Kangnung, South Korea
[5] Ajou Univ, Coll Pharm, Suwon, South Korea
关键词:
FK506;
Korean Red Ginseng;
nephrotoxicity;
MAPKs;
TACROLIMUS-INDUCED NEPHROTOXICITY;
GREEN TEA EXTRACT;
CYTOTOXICITY;
IMMUNOSUPPRESSANT;
POLYPHENOLS;
GENTAMICIN;
PATHWAY;
FK506;
D O I:
10.1016/j.jgr.2016.05.002
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
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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页码:284 / 289
页数:6
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