首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Fraction n-Butanol of Radix Notoginseng Protects PC12 Cells from Aβ25–35-Induced Cytotoxicity and Alleviates Cognitive Deficits in SAMP8 Mice by Attenuating Oxidative Stress and Aβ Accumulation
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Fraction n-Butanol of Radix Notoginseng Protects PC12 Cells from Aβ25–35-Induced Cytotoxicity and Alleviates Cognitive Deficits in SAMP8 Mice by Attenuating Oxidative Stress and Aβ Accumulation

机译:三七的正丁醇级分通过减轻氧化应激和Aβ积累来保护PC12细胞免受Aβ25-35诱导的细胞毒性并减轻SAMP8小鼠的认知缺陷。

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摘要

Chinese medicine has been used for Alzheimer's disease (AD) treatment for thousands of years with more effective and fewer side effects. Therefore, developing effective potential candidates from Chinese medicine against AD would be considered as critical and efficient therapy for AD treatment. This study was designed to evaluate the neuronal protective effect of fraction n-butanol (NB) of Radix Notoginseng on Aβ25–35-induced PC12 cells, explore the effect of the tested fraction on spatial learning and memory, and characterize the impacts of fraction NB on antioxidant enzymes, Aβ production, and APP and BACE1 expressions. The results revealed that fraction NB could promote proliferation of PC12 cells and protect and rescue PC12 cells from Aβ25–35-induced cell death. Moreover, fraction NB could improve spatial learning and memory impairments of senescence-accelerated prone8 (SAMP8) mice and attenuate oxidative stress and reduce the production of Aβ by inhibiting the expressions of APP and BACE1 in the brains of SAMP8 mice. The result of single dose acute toxicity assay showed that fraction NB had a mild toxicity in vivo. The pronounced actions against AD and in vivo low toxicity of fraction NB suggest that fraction NB may be a useful alternative to the current AD treatment.
机译:中药已被用于治疗阿尔茨海默氏病(AD)数千年,具有更有效,更小的副作用。因此,从中药开发有效的抗AD候选药物将被认为是AD治疗的关键和有效疗法。这项研究旨在评估三七的正丁醇(NB)组分对Aβ25-35诱导的PC12细胞的神经元保护作用,探讨被测组分对空间学习和记忆的影响,并表征NB组分的影响。对抗氧化酶,Aβ产生以及APP和BACE1表达的影响。结果表明,NB组分可以促进PC12细胞的增殖,并保护PC12细胞免受Aβ25-35诱导的细胞死亡。此外,NB组分可以通过抑制SAMP8小鼠大脑中APP和BACE1的表达来改善衰老加速prone8(SAMP8)小鼠的空间学习和记忆障碍,并减轻氧化应激并减少Aβ的产生。单剂量急性毒性试验的结果表明,NB组分在体内具有中等毒性。针对AD的明显作用和NB级分的体内低毒性表明NB级分可能是当前AD治疗的有用替代物。

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