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Hydroxytyrosol inhibits pro-inflammatory cytokines, iNOS, and COX-2 expression in human monocytic cells
被引:130
|作者:
Zhang, Xiaomei
[2
,3
]
Cao, Jun
[3
]
Zhong, Laifu
[1
,3
]
机构:
[1] Dalian Med Univ, Dept Toxicol, Dalian 116044, Peoples R China
[2] Dalian Univ Technol, Dept Lab Med, Coll Med, Dalian 116622, Liaoning, Peoples R China
[3] Dalian Med Univ, Dept Toxicol, Dalian 116027, Liaoning, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Hydroxytyrosol;
iNOS;
COX-2;
THP-1;
cells;
NITRIC-OXIDE SYNTHASE;
(-)-EPIGALLOCATECHIN-3-GALLATE BLOCKS;
OLIVE OIL;
CYCLO-OXYGENASE-2;
CYCLOOXYGENASE-2;
ACTIVATION;
COMPOUND;
D O I:
10.1007/s00210-009-0399-7
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Hydroxytyrosol (HT), isolated from extra-virgin olive oil, possesses a marked antioxidant activity and is a good radical scavenger. In this study, our aim was to examine the anti-inflammatory mechanism of HT through measuring the inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2) expression, TNF-alpha formation, and nitric oxide (NO) release in lipopolysaccharide (LPS)-induced human monocytic (THP-1) cells. Results showed that HT remarkably suppressed the LPS (1 mu g/ml) induction of NO release. It also significantly attenuated the LPS-induced transcription of TNF-alpha, iNOS, and COX-2 in a dose-dependent manner. Furthermore, it was also found that HT in a concentration-dependent manner inhibited the expression of iNOS and COX-2 in THP-1 cells treated with 1 mu g/ml LPS using Western Blot. Taken together, these results suggest that HT exerts anti-inflammatory effects probably through the suppression of COX-2 and iNOS expression.
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页码:581 / 586
页数:6
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