Molecular mechanisms of neuroprotection by two natural antioxidant polyphenols

被引:201
作者
Rosario Campos-Esparza, Maria
Victoria Sanchez-Gomez, Maria
Matute, Carlos [1 ]
机构
[1] Univ Basque Country, Fac Med & Odontol, Dept Neurociencias, Leioa 48940, Spain
关键词
Mangiferin; Morin; Excitotoxicity; Apoptosis; Mitochondria; Oxidative stress; NF-KAPPA-B; RAT CORTICAL-NEURONS; OXIDATIVE STRESS; NMDA RECEPTOR; GLUTAMATE NEUROTOXICITY; MYOCARDIAL-ISCHEMIA; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; CALPAIN INHIBITOR; INDUCED TOXICITY;
D O I
10.1016/j.ceca.2008.12.007
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Excessive activation of glutamate receptors, or excitotoxicity, contributes to acute and chronic neurological disorders including stroke. We previously showed that two natural polyphenol antioxidants, mangiferin and morin, are neuroprotective in a model of ischemic brain damage. In this study,we analyzed the molecular mechanisms underlying neuroprotection by mangiferin and morin in an in vitro model of excitotoxic neuronal death involving NMDA receptor overactivation. We observed that both polyphenols reduce the formation of reactive oxygen species, activate the enzymatic antioxidant system, and restore the mitochondrial membrane potential. Moreover, both antioxidants inhibit glutamate-induced activation of calpains, normalize the levels of phosphorylated Akt kinase and Erk1/2, as well as of cytosolic Bax, inhibit AIF release from mitochondria, and regulate the nuclear translocation of NF-kappa B. Each of these effects contributes to the substantial reduction of apoptotic neuronal death induced by glutamate. These results demonstrate that mangiferin and morin exhibit excellent antioxidant and antiapoptotic properties, supporting their clinical application as trial neuroprotectors in pathologies involving excitotoxic neuronal death. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:358 / 368
页数:11
相关论文
共 55 条
[1]
Mangifera indica L. extract (Vimang) inhibits Fe2+-citrate-induced lipoperoxidation in isolated rat liver mitochondria [J].
Andreu, GP ;
Delgado, R ;
Velho, J ;
Inada, NM ;
Curti, C ;
Vercesi, AE .
PHARMACOLOGICAL RESEARCH, 2005, 51 (05) :427-435
[2]
Epigallocatechin, a green tea polyphenol, attenuates myocardial ischemia reperfusion injury in rats [J].
Aneja, R ;
Hake, PW ;
Burroughs, TJ ;
Denenberg, AG ;
Wong, HR ;
Zingarelli, B .
MOLECULAR MEDICINE, 2004, 10 (1-6) :55-62
[3]
GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[4]
Methodological considerations for characterizing potential antioxidant actions of bioactive components in plant foods [J].
Aruoma, OI .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 523 :9-20
[5]
Glutamate neurotoxicity, oxidative stress and mitochondria [J].
Atlante, A ;
Calissano, P ;
Bobba, A ;
Giannattasio, S ;
Marra, E ;
Passarella, S .
FEBS LETTERS, 2001, 497 (01) :1-5
[6]
Bethea JR, 1998, J NEUROSCI, V18, P3251
[7]
Neuronal calcium mishandling and the pathogenesis of Alzheimer's disease [J].
Bezprozvanny, Ilya ;
Mattson, Mark P. .
TRENDS IN NEUROSCIENCES, 2008, 31 (09) :454-463
[8]
Curcumin induces glutathione biosynthesis and inhibits NF-κB activation and interleukin-8 release in alveolar epithelial cells:: Mechanism of free radical scavenging activity [J].
Biswas, SK ;
McClure, D ;
Jimenez, LA ;
Megson, IL ;
Rahman, I .
ANTIOXIDANTS & REDOX SIGNALING, 2005, 7 (1-2) :32-41
[9]
Micromolar L-glutamate induces extensive apoptosis in an apoptotic-necrotic continuum of insult-dependent, excitotoxic injury in cultured cortical neurones [J].
Cheung, NS ;
Pascoe, CJ ;
Giardina, SF ;
John, CA ;
Beart, PM .
NEUROPHARMACOLOGY, 1998, 37 (10-11) :1419-1429
[10]
Tournefolic acid B methyl ester attenuates glutamate-induced toxicity by blockade of ROS accumulation and abrogating the activation of caspases and JNK in rat cortical neurons [J].
Chi, CW ;
Wang, CN ;
Lin, YL ;
Chen, CF ;
Shiao, YJ .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (03) :692-700