(-) Epigallocatechin-3-gallate attenuates reserpine-induced orofacial dyskinesia and oxidative stress in rat striatum

被引:13
|
作者
Wang, Mao-Hsien [1 ,2 ]
Lin, Rui-Feng [3 ]
Tseng, Hsiang-Chien [4 ,5 ]
Soung, Hung-Sheng [6 ]
Chang, Kuo-Chi [7 ]
Tsai, Cheng-Chia [3 ,8 ]
机构
[1] En Chu Kon Hosp, Dept Anesthesia, New Taipei City 23702, Taiwan
[2] Yuanpei Univ, Dept Optometry, Hsinchu 30015, Taiwan
[3] Mackay Mem Hosp, Dept Neurosurg, Taipei 10449, Taiwan
[4] Shin Kong Wu Ho Su Mem Hosp, Dept Anesthesiol, Taipei 11101, Taiwan
[5] Fu Jan Catholic Univ, Sch Med, New Taipei City 24205, Taiwan
[6] Taipei Veteran Gen Hosp, Yuan Shan Br, Dept Psychiat, Taipei 26604, Yilan County, Taiwan
[7] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 10608, Taiwan
[8] Taipei Med Univ, Grad Inst Injury Prevent & Control, Taipei 11031, Taiwan
关键词
(-) Epigallocatechin-3-gallate; Reserpine; Orofacial dyskinesia; Lipid peroxidation; Glutathione; Superoxide dismutase; Catalase; Striatum; GREEN TEA POLYPHENOL; INDUCED ORAL DYSKINESIA; (-)-EPIGALLOCATECHIN GALLATE; MODEL; IMPAIRMENT; HALOPERIDOL; MECHANISMS; CATALASE; REVERSAL; CATECHIN;
D O I
10.1016/j.pbb.2015.02.003
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Reserpine-induced orofacial dyskinesia (OD) has been used for decades as an animal model for human tardive dyskinesia (TD) because both of them have pathophysiology strongly associated with striatal oxidative stress. Green tea catechins, especially (-) epigallocatechin-3-gallate (EGCG), have potent antioxidative effects and are able to protect against various oxidative injuries. In this study, we examined the potential protective effects of EGCG on reserpine-induced behavioral and neurochemical dysfunction in rats. Reserpine treatment (1 mg/kg s.c. one injection every other day, three injections total) induced significant increases (p < 0.001) in the frequency of vacuous chewing movement (VCM) and tongue protrusion (TP) as well as the duration of facial twitching (FT). EGCG treatment (100 mg/kg i.p. for 11 days, starting 7 days before the reserpine injections) was able to prevent most of the reserpine-induced OD. Also, EGCG treatment was able to reduce the reserpine-induced lipid peroxidation (LPO) production, and enhances the antioxidation power in the striatum of reserpine-treated rats. The above results indicate that EGCG has a protective role against reserpine-induced OD, probably via its powerful antioxidative properties. Thus, EGCG may possible have a clinically relevant therapeutic effect in preventing, delaying or even treating TD. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:71 / 76
页数:6
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