Protective Effect of Artemisia asiatica Extract and Its Active Compound Eupatilin against Cisplatin-Induced Renal Damage

Authors
Park, Jun YeonLee, DahaeJang, Hyuk-JaiJang, Dae SikKwon, Hak CheolKim, Ki HyunKim, Su-NamHwang, Gwi SeoKang, Ki SungEom, Dae-Woon
Issue Date
2015-10
Publisher
HINDAWI LTD
Citation
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, v.2015
Abstract
The present study investigated the renoprotective effect of an Artemisia asiatica extract and eupatilin in kidney epithelial (LLC-PK1) cells. Although cisplatin is effective against several cancers, its use is limited due to severe nephrotoxicity. Eupatilin is a flavonoid compound isolated from the Artemisia plant and possesses antioxidant as well as potent anticancer properties. In the LLC-PK1 cellular model, the decline in cell viability induced by oxidative stress, such as that induced by cisplatin, was significantly and dose-dependently inhibited by the A. asiatica extract and eupatilin. The increased protein expressions of phosphorylated JNK and p38 by cisplatin in cells were markedly reduced after A. asiatica extract or eupatilin cotreatment. The elevated expression of cleaved caspase-3 was significantly reduced by A. asiatica extract and eupatilin, and the elevated percentage of apoptotic cells after cisplatin treatment in LLC-PK1 cells was markedly decreased by cotreatment with A. asiatica extract or eupatilin. Taken together, these results suggest that A. asiatica extract and eupatilin could cure or prevent cisplatin-induced renal toxicity without any adverse effect; thus, it can be used in combination with cisplatin to prevent nephrotoxicity.
Keywords
GENTAMICIN-INDUCED NEPHROTOXICITY; CELL-DEATH; APOPTOSIS; ACTIVATION; EXPRESSION; DA-9601; COMPONENTS; INDUCTION; FAILURE; GINSENG; GENTAMICIN-INDUCED NEPHROTOXICITY; CELL-DEATH; APOPTOSIS; ACTIVATION; EXPRESSION; DA-9601; COMPONENTS; INDUCTION; FAILURE; GINSENG
ISSN
1741-427X
URI
https://pubs.kist.re.kr/handle/201004/124950
DOI
10.1155/2015/483980
Appears in Collections:
KIST Article > 2015
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