Institut d'Investigacions Biomèdiques de Barcelona (IIBB), CSIC and IDIBAPS, Barcelona, Spain.
CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Mol Neurobiol. 2019 Feb;56(2):1502-1516. doi: 10.1007/s12035-018-1157-y. Epub 2018 Jun 13.
Resveratrol is a natural compound that mimics the antioxidant and antiaging effects of caloric restriction, mainly mediated through SIRT1, a deacetylase that induces longevity and neuroprotection. We aimed to analyze the effects of resveratrol on the brain status of control non-transgenic (NoTg) and AD transgenic (3xTg-AD) mice to discern the mechanisms involved in a potential inducement of resilience against age-related neurodegeneration and Alzheimer's disease (AD). Mice were fed with a diet supplemented with 100 mg/kg of resveratrol from 2 months of age during 10 months. Resveratrol administration induced complete protection against memory loss and brain pathology in 3xTg-AD mice, and also induced cognitive enhancement in healthy NoTg mice. Resveratrol improved exploration and reduced anxiety in both mouse strains, indicative of well-being. Resveratrol reduced the presence of Aβ and p-tau pathology in the hippocampus of the 3xTg-AD mouse. Proteostasis analysis showed the following in both NoTg and 3xTg-AD mice: (i) increased levels of the amyloid-degrading enzyme neprilysin, (ii) reduction of the amyloidogenic secretase BACE1, and (iii) increase of proteasome protein levels and enhancement of proteasome activity. Resveratrol also increased AMPK protein levels, then upregulating the SIRT1 pathway, as shown by the activation of PGC-1α and CREB in both mice, resulting in further beneficial changes. Our data demonstrated that resveratrol induces cognitive enhancement and neuroprotection against amyloid and tau pathologies. Improvement of proteostasis by resveratrol, in both healthy and AD mice, suggests that it is a mechanism of brain resilience and defense against neurodegeneration caused by the accumulation of aberrant proteins.
白藜芦醇是一种天然化合物,可模拟热量限制的抗氧化和抗衰老作用,主要通过 SIRT1 介导,SIRT1 是一种去乙酰化酶,可诱导长寿和神经保护。我们旨在分析白藜芦醇对对照非转基因(NoTg)和 AD 转基因(3xTg-AD)小鼠大脑状态的影响,以辨别参与潜在诱导对与年龄相关的神经退行性变和阿尔茨海默病(AD)的弹性的机制。从 2 个月大开始,将 100mg/kg 的白藜芦醇添加到饮食中,连续喂食 10 个月。白藜芦醇给药可完全防止 3xTg-AD 小鼠的记忆丧失和脑病理,还可诱导健康的 NoTg 小鼠的认知增强。白藜芦醇改善了两种小鼠的探索能力并降低了焦虑感,表明其健康状况良好。白藜芦醇减少了 3xTg-AD 小鼠海马体中 Aβ和 p-tau 病理的存在。蛋白质组分析表明,两种小鼠都具有以下特征:(i)淀粉样蛋白降解酶 Neprilysin 的水平升高,(ii)淀粉样前体蛋白切割酶 BACE1 的减少,和(iii)蛋白酶体蛋白水平的增加和蛋白酶体活性的增强。白藜芦醇还增加了 AMPK 蛋白水平,然后激活 SIRT1 途径,如两种小鼠中的 PGC-1α 和 CREB 的激活所示,从而导致进一步的有益变化。我们的数据表明,白藜芦醇可增强认知并防止淀粉样蛋白和 tau 病理引起的神经损伤。白藜芦醇在健康和 AD 小鼠中改善蛋白质稳态表明,它是大脑弹性的一种机制,可防御由异常蛋白积累引起的神经退行性变。