NRF2 as a Therapeutic Target in Neurodegenerative Diseases

被引:193
作者
Brandes, Mikah S. [1 ]
Gray, Nora E. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
来源
ASN NEURO | 2020年 / 12卷
关键词
dementia and neurological disorders; neurodegenerative diseases; bioenergetics; NF-KAPPA-B; INDUCED OXIDATIVE STRESS; ALPHA-LIPOIC ACID; REMITTING MULTIPLE-SCLEROSIS; TRANSCRIPTION FACTOR NRF2; RELEASE DIMETHYL FUMARATE; PLACEBO-CONTROLLED PHASE-3; MILD COGNITIVE IMPAIRMENT; TRAUMATIC BRAIN-INJURY; COMPLEX I DEFICIENCY;
D O I
10.1177/1759091419899782
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Increased reactive oxygen species production and oxidative stress have been implicated in the pathogenesis of numerous neurodegenerative conditions including among others Alzheimer's disease, Parkinson's disease, Huntington's disease, Friedrich's ataxia, multiple sclerosis, and stroke. The endogenous antioxidant response pathway protects cells from oxidative stress by increasing the expression of cytoprotective enzymes and is regulated by the transcription factor nuclear factor erythroid 2-related factor 2 (NRF2). In addition to regulating the expression of antioxidant genes, NRF2 has also been shown to exert anti-inflammatory effects and modulate both mitochondrial function and biogenesis. This is because mitochondrial dysfunction and neuroinflammation are features of many neurodegenerative diseases as well NRF2 has emerged as a promising therapeutic target. Here, we review evidence for a beneficial role of NRF2 in neurodegenerative conditions and the potential of specific NRF2 activators as therapeutic agents.
引用
收藏
页数:23
相关论文
共 310 条
  • [1] Analysis of the role of Nrf2 in the expression of liver proteins in mice using two-dimensional gel-based proteomics
    Abdullah, Azman
    Kitteringham, Neil R.
    Jenkins, Rosalind E.
    Goldring, Christopher
    Higgins, Larry
    Yamamoto, Masayuki
    Hayes, John
    Park, B. Kevin
    [J]. PHARMACOLOGICAL REPORTS, 2012, 64 (03) : 680 - 697
  • [2] 'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'
    Abeti, R.
    Parkinson, M. H.
    Hargreaves, I. P.
    Angelova, P. R.
    Sandi, C.
    Pook, M. A.
    Giunti, P.
    Abramov, A. Y.
    [J]. CELL DEATH & DISEASE, 2016, 7 : e2237 - e2237
  • [3] Targeting lipid peroxidation and mitochondrial imbalance in Friedreich's ataxia
    Abeti, Rosella
    Uzun, Ebru
    Renganathan, Indhushri
    Honda, Tadashi
    Pook, Mark A.
    Giunti, Paola
    [J]. PHARMACOLOGICAL RESEARCH, 2015, 99 : 344 - 350
  • [4] Modulation of pentylenetetrazole-induced kindling and oxidative stress by curcumin in mice
    Agarwal, Nidhi Bharal
    Jain, Seema
    Agarwal, Nitin K.
    Mediratta, Pramod K.
    Sharma, Krishna K.
    [J]. PHYTOMEDICINE, 2011, 18 (8-9) : 756 - 759
  • [5] Transcriptomic and proteomic profiling of KEAP1 disrupted and sulforaphane-treated human breast epithelial cells reveals common expression profiles
    Agyeman, Abena S.
    Chaerkady, Raghothama
    Shaw, Patrick G.
    Davidson, Nancy E.
    Visvanathan, Kala
    Pandey, Akhilesh
    Kensler, Thomas W.
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2012, 132 (01) : 175 - 187
  • [6] [Anonymous], 2017, ALZHEIMERS DIS FACTS
  • [7] [Anonymous], FRONT NEUROSCI SWITZ
  • [8] [Anonymous], REAT ANN POS TOPL RE
  • [9] [Anonymous], AUTOIMMUNE DIS
  • [10] [Anonymous], KOREAN J HLTH ED PRO