Resveratrol inhibits MMP-9 expression by up-regulating PPAR α expression in an oxygen glucose deprivation-exposed neuron model

被引:56
作者
Cheng, Gang [1 ]
Zhang, Xiang [1 ]
Gao, Dakuan [1 ]
Jiang, Xiaofan [1 ]
Dong, Wenpeng [2 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Inst Neurosurg, Xian 710032, Shaanxi Prov, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Dept Gastrointestinal Surg, Xian 710032, Shaanxi Prov, Peoples R China
关键词
Resveratrol; Peroxisome proliferators-activated receptor; Matrix metalloproteinase; Oxygen glucose deprivation; ACTIVATED RECEPTOR-ALPHA; MATRIX-METALLOPROTEINASE INHIBITOR; CEREBRAL-ISCHEMIA; LIGAND-BINDING; FOCAL ISCHEMIA; BRAIN-DAMAGE; GAMMA; PROTEIN; STROKE; FENOFIBRATE;
D O I
10.1016/j.neulet.2008.12.045
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Resveratrol (trans-3,4',5-trihydroxystilbene, Res) is a natural polyphenol. A recent experiment confirmed that Res can selectively activate both peroxisome proliferators-activated receptors (PPAR) alpha and gamma. In addition, Res can protect neurons by matrix metalloproteinase-9 (MMP-9) down-regulation. The relationship between Res, MMP-9 and PPAR alpha or gamma was studied in an oxygen glucose deprivation-exposed neuron model. It showed that Res can inhibit mRNA and protein expression of MMP-9, while it up-regulates the expression of PPAR alpha and gamma. The effect of Res on both PPAR alpha and MMP-9 can be offset partially by MK886. However, PPAR gamma antagonist GW9662 had little effect on MMP-9 expression. These results suggest that Res can inhibit MMP-9 expression by up-regulating PPAR alpha. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:105 / 108
页数:4
相关论文
共 30 条
[1]   Rosiglitazone, a peroxisome proliferator-activated receptor-γ ligand, reduces infarction volume and neurological deficits in an embolic model of stroke [J].
Allahtavakoli, Mohammad ;
Shabanzadeh, Alireza P. ;
Sadr, Seyed Shahabeddin ;
Parviz, Mohsen ;
Djahanguiri, Bijan .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2006, 33 (11) :1052-1058
[2]   Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732
[3]  
Bradamante S, 2004, CARDIOVASC DRUG REV, V22, P169
[4]  
Cullingford TE, 1998, J NEUROCHEM, V70, P1366
[5]  
Deplanque D, 2003, J NEUROSCI, V23, P6264
[6]   Resveratrol attenuates ischemic brain damage in the delayed phase after stroke and induces messenger RNA and protein express for angiogenic factors [J].
Dong, WenPeng ;
Li, NanLin ;
Gao, DaKuan ;
Zhen, HaiNing ;
Zhang, Xiang ;
Li, FanFan .
JOURNAL OF VASCULAR SURGERY, 2008, 48 (03) :709-714
[7]   Mitochondria biogenesis induced by resveratrol against brain ischemic stroke [J].
Dong, Wenpeng ;
Gao, Dakuan ;
Zhang, Xiang .
MEDICAL HYPOTHESES, 2007, 69 (03) :700-701
[8]   In vitro cytotoxicity assays: Comparison of LDH, neutral red, MTT and protein assay in hepatoma cell lines following exposure to cadmium chloride [J].
Fotakis, G ;
Timbrell, JA .
TOXICOLOGY LETTERS, 2006, 160 (02) :171-177
[9]   Minireview -: Biological effects of resveratrol [J].
Frémont, L .
LIFE SCIENCES, 2000, 66 (08) :663-673
[10]   Structural basis for autorepression of retinoid X receptor by tetramer formation and the AF-2 helix [J].
Gampe, RT ;
Montana, VG ;
Lambert, MH ;
Wisely, GB ;
Milburn, MV ;
Xu, HE .
GENES & DEVELOPMENT, 2000, 14 (17) :2229-2241