Nrf2–ARE pathway: An emerging target against oxidative stress and neuroinflammation in neurodegenerative diseases

神经炎症 神经退行性变 氧化应激 机制(生物学) 神经科学 转录因子 生物 炎症 人口 生物信息学 医学 免疫学 疾病 基因 遗传学 内科学 哲学 认识论 环境卫生
作者
Izaskun Buendía,Patrycja Michalska,Elisa Navarro,Isabel Gameiro‐Ros,Javier Egea,Rafael León
出处
期刊:Pharmacology & Therapeutics [Elsevier]
卷期号:157: 84-104 被引量:492
标识
DOI:10.1016/j.pharmthera.2015.11.003
摘要

Neurodegenerative diseases (NDDs) are predicted to be the biggest health concern in this century and the second leading cause of death by 2050. The main risk factor of these diseases is aging, and as the aging population in Western societies is increasing, the prevalence of these diseases is augmenting exponentially. Despite the great efforts to find a cure, current treatments remain ineffective or have low efficacy. Increasing lines of evidence point to exacerbated oxidative stress, mitochondrial dysfunction and chronic neuroinflammation as common pathological mechanisms underlying neurodegeneration. We will address the role of the nuclear factor E2-related factor 2 (Nrf2) as a potential target for the treatment of NDDs. The Nrf2–ARE pathway is an intrinsic mechanism of defence against oxidative stress. Nrf2 is a transcription factor that induces the expression of a great number of cytoprotective and detoxificant genes. There are many evidences that highlight the protective role of the Nrf2–ARE pathway in neurodegenerative conditions, as it reduces oxidative stress and neuroinflammation. Therefore, the Nrf2 pathway is being increasingly considered a therapeutic target for NDDs. Herein we will review the deregulation of the Nrf2 pathway in different NDDs and the recent studies with Nrf2 inducers as “proof-of-concept” for the treatment of those devastating pathologies.
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