Resveratrol and quercetin, two natural polyphenols, reduce apoptotic neuronal cell death induced by neuroinflammation

被引:265
作者
Bureau, Genevieve [1 ]
Longpre, Fanny [1 ]
Martinoli, M. -G. [1 ,2 ]
机构
[1] Univ Quebec Trois Rivieres, Dept Biochem, Neurosci Grp, Trois Rivieres, PQ, Canada
[2] CHUL, Neurosci Unit, Quebec City, PQ, Canada
关键词
polyphenols; neuroprotection; microglia; dopaminergic neurons; Parkinson's disease;
D O I
10.1002/jnr.21503
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Parkinson's disease (PD) is a movement disorder characterized by a progressive loss of nigrostriatal dopaminergic neurons. Microglia activation and neuroinflammation have been associated with the pathogenesis of PD. Indeed, cytokines have been proposed as candidates that mediate the apoptotic cell death of dopaminergic neurons seen in PD. In this study, we investigated the effect of two natural polyphenols, resveratrol and quercetin, on neuroinflammation. For glial cells, we observed that lipopolysaccharide (LPS)-induced mRNA levels of two proinflammatory genes, interleukin 1-alpha and tumor necrosis factor-alpha, are strongly decreased by treatments with resveratrol or quercetin. We also undertook microglial-neuronal coculture to examine the influence of resveratrol and quercetin on dopaminergic neuronal cell death evoked by LPS-activated microglia. Cytotoxicity assays were performed to evaluate the percentage of cell death, with apoptotic cells identified by both the TdT-mediated dUTP nick end labeling technique and the detection of cleaved caspase-3. We report that treatment of N9 microglial cells with resveratrol or quercetin successfully reduced the inflammation-mediated apoptotic death of neuronal cells in our coculture system. Altogether our results demonstrate that resveratrol and quercetin diminished apoptotic neuronal cell death induced by microglial activation and suggest that these two phytoestrogens may be potent anti inflammatory compounds. (C) 2007Wiley-Liss, Inc.
引用
收藏
页码:403 / 410
页数:8
相关论文
共 73 条
[1]   Neurotoxic effects of lipopolysaccharide on nigral dopaminergic neurons are mediated by microglial activation, interleukin-1β, and expression of caspase-11 in mice [J].
Arai, H ;
Furuya, T ;
Yasuda, T ;
Miura, M ;
Mizuno, Y ;
Mochizuki, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :51647-51653
[2]   Interleukin-10 protects against inflammation-mediated degeneration of dopaminergic neurons in substantia nigra [J].
Arimoto, Toyoko ;
Choi, Dong-Young ;
Lu, Xin ;
Liu, Mei ;
Nguyen, Xuan V. ;
Zheng, Naiying ;
Stewart, Charles A. ;
Kim, Hyoung-Chun ;
Bing, Guoying .
NEUROBIOLOGY OF AGING, 2007, 28 (06) :894-906
[3]   Aspirin and salicylate protect against MPTP-induced dopamine depletion in mice [J].
Aubin, N ;
Curet, O ;
Deffois, A ;
Carter, C .
JOURNAL OF NEUROCHEMISTRY, 1998, 71 (04) :1635-1642
[4]   Estrogenic/antiestrogenic and scavenging properties of (E)- and (Z)-resveratrol [J].
Basly, JP ;
Marre-Fournier, F ;
Le Bail, JC ;
Habrioux, G ;
Chulia, AJ .
LIFE SCIENCES, 2000, 66 (09) :769-777
[5]   Neuroprotection against oxidative stress by estrogens: Structure-activity relationship [J].
Behl, C ;
Skutella, T ;
Lezoualch, F ;
Post, A ;
Widmann, M ;
Newton, CJ ;
Holsboer, F .
MOLECULAR PHARMACOLOGY, 1997, 51 (04) :535-541
[6]   Neuroprotective activities of estrogen: An update [J].
Behl, C ;
Manthey, D .
JOURNAL OF NEUROCYTOLOGY, 2000, 29 (5-6) :351-358
[7]   RETRACTED: Differential proteomic profiling to study the mechanism of cardiac pharmacological preconditioning by resveratrol (Retracted article. See vol. 16, pg. 2548, 2012) [J].
Bezstarosti, Karel ;
Das, Samarjit ;
Lamers, Jos. M. J. ;
Das, Dipak K. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2006, 10 (04) :896-907
[8]   Resveratrol inhibits nitric oxide and TNF-α production by lipopolysaccharide-activated microglia [J].
Bi, XL ;
Yang, JY ;
Dong, YX ;
Wang, JM ;
Cui, YH ;
Ikeshima, T ;
Zhao, YQ ;
Wu, CF .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2005, 5 (01) :185-193
[9]   Resveratrol acts as a mixed agonist/antagonist for estrogen receptors α and β [J].
Bowers, JL ;
Tyulmenkov, VV ;
Jernigan, SC ;
Klinge, CM .
ENDOCRINOLOGY, 2000, 141 (10) :3657-3667
[10]   Mitochondrial function in response to cardiac ischemia-reperfusion after oral treatment with quercetin [J].
Brookes, PS ;
Digerness, SB ;
Parks, DA ;
Darley-Usmar, V .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1220-1228