Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale F. Stagno d'Alcontres 31, 98168 Messina, Italy.
Biomolecules. 2023 Mar 17;13(3):549. doi: 10.3390/biom13030549.
Alzheimer's disease (AD) is a common neurodegenerative disorder that affects the elderly. One of the key features of AD is the accumulation of reactive oxygen species (ROS), which leads to an overall increase in oxidative damage. The nuclear factor (erythroid-derived 2)-like 2 (Nrf2) is a master regulator of the antioxidant response in cells. Under low ROS levels, Nrf2 is kept in the cytoplasm. However, an increase in ROS production leads to a translocation of Nrf2 into the nucleus, where it activates the transcription of several genes involved in the cells' antioxidant response. Additionally, Nrf2 activation increases autophagy function. However, in AD, the accumulation of Aβ and tau reduces Nrf2 levels, decreasing the antioxidant response. The reduced Nrf2 levels contribute to the further accumulation of Aβ and tau by impairing their autophagy-mediated turnover. In this review, we discuss the overwhelming evidence indicating that genetic or pharmacological activation of Nrf2 is as a potential approach to mitigate AD pathology.
阿尔茨海默病(AD)是一种常见的神经退行性疾病,影响老年人。AD 的一个关键特征是活性氧(ROS)的积累,这导致整体氧化损伤增加。核因子(红系衍生 2)样 2(Nrf2)是细胞抗氧化反应的主要调节剂。在低 ROS 水平下,Nrf2 保持在细胞质中。然而,ROS 产生的增加导致 Nrf2 易位到细胞核,在那里它激活参与细胞抗氧化反应的几个基因的转录。此外,Nrf2 的激活增加了自噬功能。然而,在 AD 中,Aβ和 tau 的积累降低了 Nrf2 水平,从而降低了抗氧化反应。减少的 Nrf2 水平通过损害其自噬介导的周转来促进 Aβ 和 tau 的进一步积累。在这篇综述中,我们讨论了大量证据表明,Nrf2 的遗传或药理学激活是减轻 AD 病理的一种潜在方法。