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

神经保护 丙二醛 缺血 人参皂甙 谷胱甘肽过氧化物酶 药理学 超氧化物歧化酶 麻醉 医学 谷胱甘肽 脑缺血 化学 内科学 人参 氧化应激 生物化学 病理 替代医学
作者
Jingwei Tian,Fenghua Fu,Meiyu Geng,Yongtao Jiang,Yang Jian-xiong,Wanglin Jiang,Chaoyun Wang,Ke Liu
出处
期刊:Neuroscience Letters [Elsevier BV]
卷期号:374 (2): 92-97 被引量:200
标识
DOI:10.1016/j.neulet.2004.10.030
摘要

This study was conducted to investigate the neuroprotective effects of 20(S)-ginsenoside Rg3 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 Rg3 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 Rg3 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 Rg3 might provide neuroprotection against the cerebral ischemia-induced injury in rat brain through reducing lipid peroxides, scavenging free radicals and improving the energy metabolism.
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