葛根素对β-淀粉样蛋白诱导大鼠海马神经元神经毒性的保护作用。

Arzneimittel-Forschung-Drug Research Pub Date : 2012-04-01 Epub Date: 2012-01-25 DOI:10.1055/s-0031-1299763
F Lin, B Xie, F Cai, G Wu
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引用次数: 26

摘要

葛根素(CAS编号3681-99-0)是从葛根中纯化出来的一种主要的异黄酮苷,具有抗氧化和雌激素样生物活性。最近的研究表明,葛根素可以保护不同类型的细胞免受各种有毒刺激引起的损伤。在本研究中,我们研究了葛根素对a β25-35诱导的海马神经元神经毒性的神经保护作用及其潜在机制。细胞暴露于a - β25-35后,细胞存活率降低,谷胱甘肽过氧化物酶(GSH-Px)和过氧化氢酶(CAT)活性降低,活性氧(ROS)的产生增加。在a - β25-35暴露之前,用葛根素对细胞进行预孵伏,提高了细胞存活率,提高了GSH-Px和CAT活性,降低了ROS的产生。先前的研究表明,糖原合成酶激酶3β (GSK-3β)的过度激活与a β诱导的细胞死亡有关。本研究发现,a - β25-35处理可提高GSK-3β活性,而经Western blot分析,葛根素预处理可阻止a - β诱导的GSK-3β活化。此外,葛根素可激活GSK-3β重要的上游激酶PKB /Akt,可能促进GSK-3β的抑制。我们的数据表明,葛根素通过多种机制减弱Aβ25-35诱导的细胞死亡,这可能有助于治疗阿尔茨海默病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effect of Puerarin on β-amyloid-induced neurotoxicity in rat hippocampal neurons.

Puerarin (CAS Number 3681-99-0), a major isoflavone glycoside purified from Pueraria lobata, was reported to possess antioxidative and estrogen-like biological activities. Recent studies showed that puerarin protects different cell types from damage caused by a variety of toxic stimuli. In the present study, we investigated the neuroprotective effect of puerarin against Aβ25-35-induced neurotoxicity in cultured hippocampal neurons, as well as the underlying mechanism(s). Following exposure of cells to Aβ25-35, cell survival and glutathione peroxidase (GSH-Px) and catalase (CAT) activities were reduced while production of reactive oxygen species (ROS) was increased. Preincubation of the cells with puerarin prior to Aβ25-35 exposure increased cell survival and GSH-Px and CAT activities and decreased ROS production. It was previously shown that overactivation of glycogen synthase kinase-3β (GSK-3β) is implicated in Aβ-induced cell death. In this study, Aβ25-35 treatment is found to increase GSK-3β activity and pretreatment with puerarin preventesAβ-induced activation of GSK-3β based on Western blot analysis. In addition, puerarin is shown to activate protein kinase B (PKB)/Akt, an important upstream kinase of GSK-3β, possibly promoting subsequent GSK-3β inhibition. Our data suggest that puerarin attenuates cell death induced by Aβ25-35 via various mechanisms, which might be beneficial for the treatment of Alzheimer's disease.

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