Adjudin attenuates lipopolysaccharide (LPS) - and ischemia-induced microglial activation

被引:44
|
作者
Shao, Jiaxiang [1 ,2 ]
Liu, Tengyuan [1 ,2 ]
Xie, Qian Reuben [1 ,2 ]
Zhang, Tingting [1 ,2 ]
Yu, Hemei [1 ,2 ]
Wang, Boshi [1 ,2 ]
Ying, Weihai [1 ,2 ]
Mruk, Dolores D. [3 ]
Silvestrini, Bruno [4 ]
Cheng, C. Yan [3 ]
Xia, Weiliang [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Med X Res Inst, Shanghai 200030, Peoples R China
[3] Populat Council, Ctr Biomed Res, Mary M Wohlford Lab Male Contracept Res, New York, NY 10065 USA
[4] Bioprogress Pharmaceut SpA, Med Chem Lab, I-03012 Anagni, Italy
关键词
Adjudin; Microglial activation; Cytokine; NF-kappa B; Brain edema; NF-KAPPA-B; FOCAL CEREBRAL-ISCHEMIA; PARKINSONS-DISEASE; PROTEIN-KINASES; CELL-ADHESION; BRAIN EDEMA; INHIBITION; STROKE; MICE; INFLAMMATION;
D O I
10.1016/j.jneuroim.2012.09.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neuroinflammation caused by microglial activation plays a key role in ischemia, neurodegeneration and many other CNS diseases. In this study, we found that Adjudin, a potential non-hormonal male contraceptive, exhibits additional function to reduce the production of proinflammatory mediators. Adjudin significantly inhibited LPS-induced IL-6 release and IL-6, IL-1 beta, TNF-alpha expression in BV2 microglial cells. Furthermore, Adjudin exhibited anti-inflammatory properties by suppression of NF-kappa B p65 nuclear translocation and DNA binding activity as well as ERK MAPK phosphorylation. To determine the in vivo effect of Adjudin, we used a permanent middle cerebral artery occlusion (pMCAO) mouse model and found that Adjudin could reduce ischemia-induced CD11b expression, a marker of microglial activation. Furthermore, Adjudin treatment attenuated brain edema and neurological deficits after ischemia but did not reduce infarct volume. Thus, our data suggest that Adjudin may be useful for mitigating neuroinflammation. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 90
页数:8
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