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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Antiamnesic Effect of Actinidia arguta Extract Intake in a Mouse Model of TMT-Induced Learning and Memory Dysfunction
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Antiamnesic Effect of Actinidia arguta Extract Intake in a Mouse Model of TMT-Induced Learning and Memory Dysfunction

机译:Actinidia Arguta提取物摄入在TMT诱导的学习记忆功能障碍小鼠模型中的抗杀伤作用

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摘要

The antiamnesic effects of ethyl acetate fraction from Actinidia arguta (EFAA) on trimethyltin- (TMT-) induced memory impairment were investigated to find the possibility of functional food substances. EFAA showed a potent AChE inhibitory effect (IC50 = 53 mu g/mL) and efficient neuroprotection against H2O2-induced oxidative stress. The administration of EFAA significantly decreased TMT-induced cognitive deficit in Y-maze, passive avoidance, and Morris water maze (MWM) tests. After the behavioral tests, the antioxidant activities were confirmed using mice brain tissues. EFAA not only showed the inhibition of AChE activity and the decline of malondialdehyde (MDA) level as a sign of lipid peroxidation but also presented the increase of the superoxide dismutase (SOD) level and the decrease of the oxidized glutathione (GSSG)/total glutathione (GSH + GSSG) ratio. Finally, the phenolics in EFAA were identified using liquid chromatography coupled with hybrid triple quadrupole-linear ion trap mass spectrometry, and four main phenolics, such as quinic acid, chlorogenic acid, caffeoyl hexose, and quercetin-3-glucoside, were identified. These results suggest that EFAA containing physiological phenolics might enhance drug-induced amnesia through AChE inhibition and neuroprotection.
机译:研究了Actinidia Arguta(EFAA)对三甲基锡(TMT-)诱导的记忆损伤的抗醋酸乙酯级分的抗抗动癖效应,以发现功能性食品的可能性。 EFAA显示出有效的疼痛抑制作用(IC50 =53μg/ mL),有效的神经保护诱导的H2O2诱导的氧化应激。 EFAA的给药显着降低了Y型迷宫,被动避免和莫里斯水迷宫(MWM)试验中的TMT引起的认知缺陷。在行为试验后,使用小鼠脑组织确认抗氧化活性。 EFAA不仅表现出疼痛活性的抑制和丙二醛(MDA)水平作为脂质过氧化的迹象,而且还提出了超氧化物歧化酶(SOD)水平的增加和氧化谷胱甘肽(GSSG)/总谷胱甘肽的降低(GSH + GSSG)比率。最后,使用液相色谱法使用与杂交三巨胶 - 线性离子阱质谱法鉴定EFAA中的酚类,并鉴定了四种主要酚类,例如醋酸,绿原酸,咖啡酰己糖和槲皮素-3-葡糖苷。这些结果表明,含有生理酚类的EFAA可以通过疼痛抑制和神经保护剂来增强药物诱导的胃癌。

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    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

    Gyeongsang Natl Univ Ctr Res Facil Jinju 660701 South Korea;

    Kyung Hee Univ Dept Food Sci &

    Biotechnol Yongin 446701 South Korea;

    Gyeongsang Natl Univ Inst Agr &

    Life Sci Div Appl Life Sci Jinju 660701 South Korea;

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  • 正文语种 eng
  • 中图分类 临床医学;
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