Effects of Astaxanthin on the Production of NO and the Expression of COX-2 and iNOS in LPS-Stimulated BV2 Microglial Cells

被引:87
作者
Choi, Seok-Keun [1 ]
Park, Young-Sam [1 ]
Choi, Dong-Kug [2 ]
Chang, Hyo-Ihl [1 ]
机构
[1] Korea Univ, Dept Biotechnol, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
[2] Konkuk Univ, Dept Biotechnol, Chungju 380701, Chung Buk, South Korea
关键词
Astaxanthin; anti-inflammatory activity; BV2 microglial cell; Inflammatory mediator;
D O I
10.4014/jmb.0800.489
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Astaxanthin has shown antioxidant, antitumor, and anti-inflammatory activities; however, its molecular action and mechanism in the nervous system have yet to be elucidated. We examined the in vitro effects of astaxanthin on the production of nitric oxide (NO), as well as the expression of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) in lipopolysaccharide (LPS)-stimulated BV2 microglial cells. Astaxanthin inhibited the expression or formation of nitric oxide (NO), iNOS and COX-2 in lipopolysaccharide (LPS)-stimulated BV-2 microglial cells. Astaxanthin also suppressed the protein levels of iNOS and COX-2 in LPS-stimulated BV2 microglial cells. These results suggest that astaxanthin, probably due to its antioxidant activity, inhibits the production of inflammatory mediators by blocking iNOS and COX-2 activation or by the suppression of iNOS and COX-2 degradation.
引用
收藏
页码:1990 / 1996
页数:7
相关论文
共 23 条
[1]  
[Anonymous], 1996, Methods in nitric oxide research
[2]   Role of macrophages/microglia in multiple sclerosis and experimental allergic encephalomyelitis [J].
Benveniste, EN .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1997, 75 (03) :165-173
[3]   In vivo regulation of vasomotricity by nitric oxide and prostanoids during gestation [J].
Boujedaini, N ;
Liu, J ;
Thuillez, C ;
Cazin, L ;
Mensah-Nyagan, AG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 427 (02) :143-149
[4]  
BOYLE EA, 1990, AM J PATHOL, V137, P575
[5]   Inhibition of nitric oxide synthase inhibitors and lipopolysaccharide induced inducible NOS and cyclooxygenase-2 gene expressions by rutin, quercetin, and quercetin pentaacetate in RAW 264.7 macrophages [J].
Chen, YC ;
Shen, SC ;
Lee, WR ;
Hou, WC ;
Yang, LL ;
Lee, TJF .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2001, 82 (04) :537-548
[6]   Synthetic wogonin derivatives suppress lipopolysaccharide-induced nitric oxide production and hydrogen peroxide-induced cytotoxicity [J].
Chun, W ;
Lee, HJ ;
Kong, PJ ;
Lee, GH ;
Cheong, IY ;
Park, H ;
Kim, SS .
ARCHIVES OF PHARMACAL RESEARCH, 2005, 28 (02) :216-219
[7]  
Combs CK, 2001, J NEUROSCI, V21, P1179
[8]  
Feldmann M, 1998, Int Rev Immunol, V17, P217, DOI 10.3109/08830189809084493
[9]   DIFFUSE MICROGLIOSIS ASSOCIATED WITH CEREBRAL ATROPHY IN THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME [J].
GELMAN, BB .
ANNALS OF NEUROLOGY, 1993, 34 (01) :65-70
[10]   Microglia as mediators of inflammatory and degenerative diseases [J].
González-Scarano, F ;
Baltuch, G .
ANNUAL REVIEW OF NEUROSCIENCE, 1999, 22 :219-240