Green tea polyphenols inhibit cognitive impairment induced by chronic cerebral hypoperfusion via modulating oxidative stress

被引:118
作者
Xu, Yan [1 ]
Zhang, Jun-Jian [1 ]
Xiong, Li [2 ]
Zhang, Lei [2 ]
Sun, Dong [2 ]
Liu, Hui [2 ]
机构
[1] Wuhan Univ, Dept Neurol, Zhongnan Hosp, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Neuropsychol Res Ctr, Wuhan 430071, Peoples R China
关键词
Green tea polyphenols; Learning and memory; Chronic cerebral hypoperfusion; Free radicals; Antioxidation; ALZHEIMERS-DISEASE; VASCULAR DISORDER; WHITE-MATTER; RATS; CATECHINS; ISCHEMIA; BRAIN; DAMAGE; MODEL; SENESCENCE;
D O I
10.1016/j.jnutbio.2009.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Responses to oxidative stress contribute to damage caused by chronic cerebral hypoperfusion, which is characteristic of certain neurodegenerative diseases. We used a rat model of chronic cerebral hypoperfusion to determine whether green tea polyphenols, which are potent antioxidants and free radical scavengers, can reduce vascular cognitive impairment and to investigate their underlying mechanisms of action. Different doses of green tea polyphenols were administered orally to model rats from 4 to 8 weeks after experimentally induced cerebral hypoperfusion, and spatial learning and memory were assessed using the Morris water maze. Following behavioral testing, oxygen free radical levels and antioxidative capability in the cortex and hippocampus were measured biochemically. The levels of lipid peroxidation and oxidative DNA damage were assessed by immunohistochemical staining for 4-hydroxynonenal and 8-hydroxy-2'-deoxyguanosine, respectively. Rats that received green tea polyphenols 400 mg/kg per day had better spatial learning and memory than saline-treated rats. Green tea polyphenols 400 mg/kg per day were found to scavenge oxygen free radicals, enhance antioxidant potential, decrease lipid peroxide production and reduce oxidative DNA damage. However, green tea polyphenols 100 mg/kg per day had no significant effects, particularly in the cortex. This study suggests that green tea polyphenols 400 mg/kg per day improve spatial cognitive abilities following chronic cerebral hypoperfusion and that these effects may be related to the antioxidant effects of these compounds. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:741 / 748
页数:8
相关论文
共 38 条
  • [1] Green tea catechins partially protect DNA from (.)OH radical-induced strand breaks and base damage through fast chemical repair of DNA radicals
    Anderson, RF
    Fisher, LJ
    Hara, Y
    Harris, T
    Mak, WB
    Melton, LD
    Packer, JE
    [J]. CARCINOGENESIS, 2001, 22 (08) : 1189 - 1193
  • [2] Neuroprotective effects of green and black teas and their catechin gallate esters against β-amyloid-induced toxicity
    Bastianetto, S
    Yao, ZX
    Papadopoulos, V
    Quirion, R
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (01) : 55 - 64
  • [3] Buege J A, 1978, Methods Enzymol, V52, P302
  • [4] Oxidative damage to the c-fos gene and reduction of its transcription after focal cerebral ischemia
    Cui, JK
    Holmes, EH
    Liu, PK
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 73 (03) : 1164 - 1174
  • [5] DE TJ, 1999, ACTA NEUROPATHOL, V98, P1
  • [6] DE TJ, 2000, ANN NY ACAD SCI, V903, P424
  • [7] Reduction of cerebral infarction in rats by biliverdin associated with amelioration of oxidative stress
    Deguchi, Kentaro
    Hayashi, Takeshi
    Nagotani, Shoko
    Sehara, Yoshihide
    Zhany, HanZhe
    Tsuhciya, Atsushi
    Ohta, Yasuyuki
    Tomiyama, Koji
    Morimoto, Nobutoshi
    Miyazaki, Masahiro
    Huh, Nam-Ho
    Nakao, Atsunori
    Kamiya, Tatsushi
    Abe, Koji
    [J]. BRAIN RESEARCH, 2008, 1188 : 1 - 8
  • [8] Cerebral microvascular pathology in aging and Alzheimer's disease
    Farkas, E
    Luiten, PGM
    [J]. PROGRESS IN NEUROBIOLOGY, 2001, 64 (06) : 575 - 611
  • [9] Permanent, bilateral common carotid artery occlusion in the rat: A model for chronic cerebral hypoperfusion-related neurodegenerative diseases
    Farkas, Eszter
    Luiten, Paul G. M.
    Bari, Ferenc
    [J]. BRAIN RESEARCH REVIEWS, 2007, 54 (01) : 162 - 180
  • [10] Oxidative stress and cerebrovascular dysfunction in mouse models of Alzheimer's disease
    Hamel, E.
    Nicolakakis, N.
    Aboulkassim, T.
    Ongali, B.
    Tong, X-K.
    [J]. EXPERIMENTAL PHYSIOLOGY, 2008, 93 (01) : 116 - 120