Nargenicin attenuates lipopolysaccharide-induced inflammatory responses in BV-2 cells

被引:8
|
作者
Yoo, Jin Cheol [2 ]
Cho, Hong-Suk [1 ]
Park, Euteum [1 ]
Park, Jeong Ae [1 ]
Kim, Seung [1 ]
Kim, Do Kyung [3 ]
Kim, Chun Sung [4 ]
Kim, Sung-Jun [1 ]
Chun, Hong Sung [1 ,5 ]
机构
[1] Chosun Univ, Dept Biotechnol, Coll Nat Sci, Program BK21, Kwangju 501759, South Korea
[2] Chosun Univ, Coll Pharm, Dept Pharm, Kwangju 501759, South Korea
[3] Chosun Univ, Coll Dent, Dept Oral Physiol, Kwangju 501759, South Korea
[4] Chosun Univ, Coll Dent, Dept Oral Biochem, Kwangju 501759, South Korea
[5] Chosun Univ, Res Ctr Proteineous Mat, Kwangju 501759, South Korea
关键词
BV-2; cells; cytokines; lipopolysaccharide; nargenicin; nitric oxide; NITRIC-OXIDE SYNTHASE; PARKINSONS-DISEASE; MICROGLIAL CELLS; INNATE IMMUNITY; KAPPA-B; DEATH; LPS; NEURODEGENERATION; ACTIVATION; INDUCTION;
D O I
10.1097/WNR.0b013e32832d2239
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglia activation has been considered as a major factor associated with neurodegenerative diseases. In this study, we investigated the inhibitory effects of nargenicin, a natural antibiotic from soil bacterium Nocardia, on lipopolysaccharide (LPS)-induced inflammatory activation of microglia. Nargenicin significantly attenuated LIPS-induced nitric oxide production in BV-2 microglial cells. Furthermore, nargenicin effectively suppressed the upregulation of interleukin-1 beta, tumor necrosis factor alpha, and inducible nitric oxide synthase at both mRNA and protein levels in LIPS-stimulated BV-2 microglia. In addition, nargenicin blocked LPS-induced degradation of I kappa B-alpha, indicating that the initial molecular target of nargenicin is the transcription factor nuclear factor-kappa B. These results suggest that nargenicin should be evaluated as a therapeutic agent for inflammatory neurodegenerative diseases. NeuroReport 20:1007-1012 (C) 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:1007 / 1012
页数:6
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