首页> 美国卫生研究院文献>Oxidative Medicine and Cellular Longevity >Tiliacora triandra an Anti-Intoxication Plant Improves Memory Impairment Neurodegeneration Cholinergic Function and Oxidative Stress in Hippocampus of Ethanol Dependence Rats
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Tiliacora triandra an Anti-Intoxication Plant Improves Memory Impairment Neurodegeneration Cholinergic Function and Oxidative Stress in Hippocampus of Ethanol Dependence Rats

机译:Tiliacora triandra一种抗毒植物可改善乙醇依赖大鼠海马的记忆障碍神经退行性疾病胆碱能功能和氧化应激。

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摘要

Oxidative stress plays an important role in brain dysfunctions induced by alcohol. Since less therapeutic agent against cognitive deficit and brain damage induced by chronic alcohol consumption is less available, we aimed to assess the effect of Tiliacora triandra extract, a plant possessing antioxidant activity, on memory impairment, neuron density, cholinergic function, and oxidative stress in hippocampus of alcoholic rats. Male Wistar rats were induced ethanol dependence condition by semivoluntary intake of alcohol for 15 weeks. Alcoholic rats were orally given T. triandra at doses of 100, 200, and 400 mg·kg−1BW for 14 days. Memory assessment was performed every 7 days while neuron density, activities of AChE, SOD, CAT, and GSH-Px and, MDA level in hippocampus were assessed at the end of study. Interestingly, the extract mitigated the increased escape latency, AChE and MDA level. The extract also mitigated the decreased retention time, SOD, CAT, and GSH-Px activities, and neurons density in hippocampus induced by alcohol. These data suggested that the extract improved memory deficit in alcoholic rats partly via the decreased oxidative stress and the suppression of AChE. Therefore, T. triandra is the potential reagent for treating brain dysfunction induced by alcohol. However, further researches are necessary to understand the detail mechanism and possible active ingredient.
机译:氧化应激在酒精引起的脑功能障碍中起重要作用。由于较少的治疗剂可减少因慢性饮酒引起的认知缺陷和脑损伤的治疗方法,因此我们旨在评估具有抗氧化活性的植物T树提取物对记忆障碍,神经元密度,胆碱能功能和氧化应激的影响。酒精性大鼠海马。雄性Wistar大鼠通过半自愿饮酒15周诱导出乙醇依赖状态。酒精性大鼠口服百日咳铁锈菌剂量分别为100、200和400μmg·kg -1 BW,持续14天。每7天进行一次记忆评估,同时在研究结束时评估海马神经元密度,AChE,SOD,CAT和GSH-Px的活性以及MDA水平。有趣的是,提取物减轻了逃逸潜伏期,AChE和MDA水平的增加。提取物还减轻了酒精引起的海马停留时间,SOD,CAT和GSH-Px活性以及神经元密度的减少。这些数据表明,该提取物部分通过减少氧化应激和抑制AChE改善了酒精中毒大鼠的记忆障碍。因此,T。triandra是治疗酒精引起的脑功能障碍的潜在试剂。但是,需要进一步的研究来了解其详细机理和可能的活性成分。

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