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Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro.

Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro. Research Abstract Details 

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  • Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro. Abstract Text:

    chaoyun wangChaoyun Wang,dalei zhangDalei Zhang,hongmei maHongmei Ma,juntian liuJuntian Liu,chaoyun wangChaoyun Wang,dalei zhangDalei Zhang,hongmei maHongmei Ma,juntian liuJuntian Liu,

    Emodin-8-O-beta-D-glucoside extracted from the traditional Chinese medicinal herb Polygonum cuspidatum Sieb. et Zucc is widely used to treat acute hepatitis possibly by antioxidative mechanisms. The present study was designed to investigate whether emodin-8-O-beta-D-glucoside exerted neuroprotective effects on the focal cerebral injury induced by ischemia and reperfusion in vivo and on the neuronal damage induced by glutamate in vitro, and to study the possible mechanisms. Male Wistar rats were used to establish the model of ischemia and reperfusion. The behavioral test was performed and the cerebral infarction area was assessed in the brain slices stained with 2% 2,3,5-triphenyl tetrazolium chloride to evaluate the neuroprotective effects of emodin-8-O-beta-D-glucoside. Superoxide dismutase (SOD) activity, total antioxidative capability and malondialdehyde (MDA) level in the brain tissue were determined with spectrophotometrical methods to probe the primary mechanisms of emodin-8-O-beta-D-glucoside. In vitro, the neuroprotective effects of emodin-8-O-beta-D-glucoside were tested in the cultured cortical cells of fetal rats exposed to glutamate. Emodin-8-O-beta-D-glucoside concentration in plasma and brain tissue was also measured to examine distribution of emodin-8-O-beta-D-glucoside in the brain. The results showed that the treatment of rats with emodin-8-O-beta-D-glucoside reduced the neurological deficit score and the cerebral infarction area, increased SOD activity and total antioxidative capability, and decreased MDA level in the brain tissue in dose-dependent way. Emodin-8-O-beta-D-glucoside also inhibited the neuronal damage induced by glutamate. Besides, emodin-8-O-beta-D-glucoside was able to penetrate blood-brain barrier and distribute in the brain tissue. These findings demonstrate that emodin-8-O-beta-D-glucoside is able to provide neuroprotection against cerebral ischemia-reperfused injury and glutamate induced neuronal damage through exerting antioxidative effects and inhibiting glutamate neurotoxicity.

    Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro. Publishing Authors By Initials

    c wangC Wang,d zhangD Zhang,h maH Ma,j liuJ Liu,c wangC Wang,d zhangD Zhang,h maH Ma,j liuJ Liu,

    For similar abstracts research abstracts see: abstracts research

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    Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: European journal of pharmacology

    VOLUME: 577

    Page Numbers: 58-63

    Journal Abbreviation: Eur. J. Pharmacol.

    ISSN: 0014-2999

    DAY: 11

    MONTH: 09

    YEAR: 2007

    Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro. Information

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    LANGUAGE: eng

    NlmUniqueID: 1254354

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    Grant and Affiliation Information for Neuroprotective effects of emodin-8-O-beta-D-glucoside in vivo and in vitro.

    AFFILIATION: Xi'an Jiaotong University School of Medicine, Xi'an Shaanxi 710061, PR China.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Eur J Pharmacol

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