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葛根素对β-淀粉样蛋白诱导的大鼠海马神经元神经毒性的保护作用。

Protective effect of Puerarin on β-amyloid-induced neurotoxicity in rat hippocampal neurons.

作者信息

Lin F, Xie B, Cai F, Wu G

机构信息

Beijing Institute of Technology, Beijing, People's Republic of China.

出版信息

Arzneimittelforschung. 2012 Apr;62(4):187-93. doi: 10.1055/s-0031-1299763. Epub 2012 Jan 25.

Abstract

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.

摘要

葛根素(CAS编号3681-99-0)是从野葛中纯化得到的一种主要异黄酮苷,据报道具有抗氧化和雌激素样生物活性。最近的研究表明,葛根素可保护不同细胞类型免受多种毒性刺激造成的损伤。在本研究中,我们研究了葛根素对培养的海马神经元中Aβ25-35诱导的神经毒性的神经保护作用及其潜在机制。细胞暴露于Aβ25-35后,细胞存活率、谷胱甘肽过氧化物酶(GSH-Px)和过氧化氢酶(CAT)活性降低,而活性氧(ROS)生成增加。在Aβ25-35暴露前用葛根素预孵育细胞可提高细胞存活率、GSH-Px和CAT活性,并减少ROS生成。先前研究表明,糖原合酶激酶-3β(GSK-3β)的过度激活与Aβ诱导的细胞死亡有关。在本研究中,基于蛋白质印迹分析发现,Aβ25-35处理可增加GSK-3β活性,而用葛根素预处理可防止Aβ诱导的GSK-3β激活。此外,葛根素可激活蛋白激酶B(PKB)/Akt,这是GSK-3β的一种重要上游激酶,可能促进随后对GSK-3β的抑制。我们的数据表明,葛根素通过多种机制减轻Aβ25-35诱导的细胞死亡,这可能对阿尔茨海默病的治疗有益。

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