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Piperine protects cisplatin-induced apoptosis via heme oxygenase-1 induction in auditory cells
被引:63
作者:
Choi, Byung-Min
Kim, Sung-Min
Park, Tae-Kwang
Li, Guang
Hong, Sung-Jae
Park, Raekil
Chung, Hun-Taeg
Kim, Bok-Ryang
[1
]
机构:
[1] Wonkwang Univ, Sch Med, Dept Biochem, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Sch Med, Dept Microbiol & Immunol, Iksan 570749, Chonbuk, South Korea
关键词:
cisplatin;
heme oxygenase;
MAPK;
Nrf2;
piperine;
D O I:
10.1016/j.jnutbio.2006.11.012
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Piperine is a major component of black pepper, Piper nigrum Linn, used widely in traditional medicine. In this study, we examined whether piperine could protect House Ear Institute-Organ of Corti I (HET-OCI) cells against cisplatin-induced apoptosis through the induction of heme oxygenase (HO)-1 expression. Piperine (10-100 mu M) induced the expression of HO-I in dose- and time-dependent manners. Piperine also induced antioxidant response element-luciferase and translocated nuclear factor-E2-related factor-2 (Nrf2) to nucleus. Piperine activated the c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase and p38 mitogen-activated protein kinase (MAPK) pathways, and the JNK pathway played an important role in piperine-induced HO-I expression. Piperine protected the cells against cisplatin-induced apoptosis. The protective effect of piperine was abrogated by zinc protoporphyrin IX, an HO inhibitor, and antisense oligodeoxynucleotides against HO-I gene. These results demonstrate that the expression of HO-I by piperine is mediated by both JNK pathway and Nrf2, and the expression inhibits cisplatin-induced apoptosis in HEI-OCl cells. (c) 2007 Elsevier Inc. All rights reserved.
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页码:615 / 622
页数:8
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