Neuroprotective effect of 20(S)-ginseno side Rg3 on cerebral ischemia in rats

被引:172
作者
Tian, JW
Fu, FH
Geng, MY
Jiang, YT
Yang, JX
Jiang, WL
Wang, CY
Liu, K
机构
[1] Yantai Univ, Sch Pharm, Shandong 246003, Peoples R China
[2] Ocean Univ China, Marine Drug & Food Inst, Shandong, Peoples R China
[3] Shaanxi Normal Univ, Coll Life Sci, Xian, Shaanxi, Peoples R China
关键词
20(S)-ginsenoside Rg(3); cerebral ischemia; energy metabolism; free radical; neuroprotection; mitchondrial;
D O I
10.1016/j.neulet.2004.10.030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study was conducted to investigate the neuroprotective effects of 20(S)-ginsenoside Rg(3) on focal cerebral ischemia in rats. Middle cerebral artery occlusion (MCAO) model in male Wistar-Kyoto (WKY) rats was employed. The behavioral tests were used to evaluate the damage to central nervous system. The infarct area of brain was assessed in the brain slices stained with 2,3,5-triphenyltetrazolium chloride (TTC). Hydrogen clearance techniques were used to monitor regional cerebral blood flow (rCBF), spectrophotometric assay methods were used to determine the activities of superoxide dismutase (SOD) and glutathione-peroxidase (GSH-Px), contents of malondialdehyde (MDA) and adenosine triphosphate (ATP) of the brain. Furthermore, the respiratory control ratio (RCR =State 3/State 4) was assessed in the brain mitochondria. The results showed that sublingual vein injection of 20(S)-ginsenoside Rg(3) at doses of 10 and 5 mg kg(-1), but not 2.5 mg kg(-1) exhibited significant neuroprotective effects on rats against focal cerebral ischemic injury by markedly decreasing neurological deficit scores, reducing the infarct area and enhancing the rCBF compared with the control group. At the same time, 20(S)-ginsenoside Rg(3) significantly improved mitochondrial energy metabolism, antagonized decreases in SOD and GSH-Px activities and increase in MDA level induced by cerebral ischemia. All these findings suggest that 20(S)-ginsenoside Rg(3) might provide neuroprotection against the cerebral ischemia-induced injury in rat brain through reducing lipid peroxides, scavenging free radicals and improving the energy metabolism. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:92 / 97
页数:6
相关论文
共 21 条
[1]   RAT MIDDLE CEREBRAL-ARTERY OCCLUSION - EVALUATION OF THE MODEL AND DEVELOPMENT OF A NEUROLOGIC EXAMINATION [J].
BEDERSON, JB ;
PITTS, LH ;
TSUJI, M ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, H .
STROKE, 1986, 17 (03) :472-476
[2]   Role of oxidants in ischemic brain damage [J].
Chan, PH .
STROKE, 1996, 27 (06) :1124-1129
[3]   Effects of naloxone on lactate, pyruvate metabolism and antioxidant enzyme activity in rat cerebral ischemia/reperfusion [J].
Chen, CJ ;
Cheng, FC ;
Liao, SL ;
Chen, WY ;
Lin, NN ;
Kuo, JS .
NEUROSCIENCE LETTERS, 2000, 287 (02) :113-116
[4]  
Chen YH, 2000, ACTA PHARMACOL SIN, V21, P463
[5]  
CLARK JB, 1970, J BIOL CHEM, V245, P4724
[6]   Inhibition of glutamate release via recovery of ATP levels accounts for a neuroprotective effect of aspirin in rat cortical neurons exposed to oxygen-glucose deprivation [J].
De Cristóbal, J ;
Cárdenas, A ;
Lizasoain, I ;
Leza, JC ;
Fernández-Tomé, P ;
Lorenzo, P ;
Moro, MA .
STROKE, 2002, 33 (01) :261-267
[7]   A RAPID METHOD FOR PREPARING SYNAPTOSOMES - COMPARISON, WITH ALTERNATIVE PROCEDURES [J].
DODD, PR ;
HARDY, JA ;
OAKLEY, AE ;
EDWARDSON, JA ;
PERRY, EK ;
DELAUNOY, JP .
BRAIN RESEARCH, 1981, 226 (1-2) :107-118
[8]   AN AUTOMATED-ANALYSIS OF GLUTATHIONE-PEROXIDASE, S-TRANSFERASE, AND REDUCTASE-ACTIVITY IN ANIMAL TISSUE [J].
JASKOT, RH ;
CHARLET, EG ;
GROSE, EC ;
GRADY, MA ;
ROYCROFT, JH .
JOURNAL OF ANALYTICAL TOXICOLOGY, 1983, 7 (02) :86-88
[9]  
Jung KY, 1998, BIOL PHARM BULL, V21, P79, DOI 10.1248/bpb.21.79
[10]   Inhibition of stress-induced plasma corticosterone levels by ginsenosides in mice: involvement of nitric oxide [J].
Kim, DH ;
Jung, JS ;
Suh, HW ;
Huh, SO ;
Min, SK ;
Son, BK ;
Park, JH ;
Kim, ND ;
Kim, YH ;
Song, DK .
NEUROREPORT, 1998, 9 (10) :2261-2264