Role of Nrf2 in Neurodegenerative Diseases

A special issue of Antioxidants (ISSN 2076-3921). This special issue belongs to the section "Health Outcomes of Antioxidants and Oxidative Stress".

Deadline for manuscript submissions: 20 April 2025 | Viewed by 2742

Special Issue Editors


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Guest Editor
Department of Pathology, Grossman School of Medicine, New York University, New York, NY 10016, USA
Interests: Alzheimer's disease; amyloidosis; neurodegenerative disorders; mitochondrial dysfunction; oxidative stress; cerebral amyloid angiopathy; neuroinflammation

E-Mail Website
Guest Editor
Department of Pathology, Grossman School of Medicine, New York University, New York, NY 10016, USA
Interests: Alzheimer disease; neurodegenerative disorders; systemic and cerebral amyloidoses; aging; proteomics; post-translational modifications; blood-brain-barrier; amyloid; neurofibrillary tangles; cerebral amyloid angiopathy; cerebral hemorrhage; translational approaches; mouse models
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Special Issue Information

Dear Colleagues,

In recent decades, the incidence of neurodegenerative disorders, including Alzheimer’s and Parkinson’s diseases, vascular dementia, and amyotrophic lateral sclerosis, among others, has remarkably increased worldwide. Despite extensive research, the complex molecular mechanisms driving the pathogenesis of these disorders have not been fully elucidated and disease-modifying therapeutic strategies remain to be discovered. Among the different pathways compromised in this diverse group of neurodegenerative diseases, mounting evidence highlights a central role of mitochondrial detrimental changes, oxidative stress, altered cerebral glucose metabolism, and metabolic/bioenergetic shifts that frequently precede cognitive abnormalities. The central element interlinking these complex pathways is Nrf2 (nuclear factor erythroid 2-related factor 2), a critical transcription factor that coordinates the expression of more than 500 cytoprotective and metabolic genes modulating inducible defence systems and regulating not only the antioxidant response but also mitochondria functioning as well as multiple points of the cell intermediary metabolism.

This Special Issue aims to provide insight into the role of Nrf2 in the interplay between the multifaceted molecular pathways linking metabolic/bioenergetic alterations, neuroinflammatory mechanisms, vascular dysfunction, and cognitive impairment associated with neurodegeneration. Manuscripts addressing the clinical implications and therapeutic potential of targeting the Nrf2 signaling pathway in neurodegenerative conditions are also of interest. We welcome contributions in the form of original research articles, reviews, and perspectives.

Dr. Agueda A. Rostagno
Prof. Dr. Jorge Ghiso
Guest Editors

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Keywords

  • Nrf2 pathway
  • nuclear factor erythroid 2-related factor 2
  • neuroprotection
  • Parkinson’s disease
  • Alzheimer’s disease
  • neurodegenerative diseases
  • neuroinflammation
  • metabolic/bioenergetic alterations
  • oxidative stress
  • mitochondria
  • amyotrophic lateral sclerosis

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Published Papers (2 papers)

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Research

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16 pages, 3869 KiB  
Article
α-Cyclodextrin/Moringin Induces an Antioxidant Transcriptional Response Activating Nrf2 in Differentiated NSC-34 Motor Neurons
by Agnese Gugliandolo, Gabriella Calì, Claudia Muscarà, Osvaldo Artimagnella, Patrick Rollin, Daniele Perenzoni, Renato Iori, Emanuela Mazzon and Luigi Chiricosta
Antioxidants 2024, 13(7), 813; https://doi.org/10.3390/antiox13070813 - 6 Jul 2024
Cited by 1 | Viewed by 1041
Abstract
Oxidative stress is a common feature of neurodegenerative diseases. Different natural compounds mediate neuroprotective effects by activating the Nrf2 antioxidant response. Some isothiocyanates are Nrf2 activators, including Moringin (MOR). In this study, the transcriptional profile of differentiated NSC-34 motor neurons was evaluated after [...] Read more.
Oxidative stress is a common feature of neurodegenerative diseases. Different natural compounds mediate neuroprotective effects by activating the Nrf2 antioxidant response. Some isothiocyanates are Nrf2 activators, including Moringin (MOR). In this study, the transcriptional profile of differentiated NSC-34 motor neurons was evaluated after treatment for 48 h and 96 h with concentrations of 0.5, 5, and 10 µM of a new MOR formulation obtained with α-cyclodextrin (α-CD). All the concentrations increased gene expression and cytoplasmic protein levels of Nrf2 at 96 h. However, the highest dose also increased nuclear Nrf2 levels at 96 h. Then, Nrf2 interactors were selected using STRING, and common biological process (BP) terms between the groups were evaluated. α-CD/MOR was able to modulate BP related to responses to oxidative stress, proteostasis, and autophagy. Specifically, the treatment with 10 µM of α-CD/MOR for 96 h induced genes involved in glutathione synthesis and proteasome subunits and reduced the expression of genes related to endoplasmic reticulum stress. Moreover, this group showed the lowest levels of the apoptotic markers Bax, cleaved caspase 9, and cleaved caspase 3. These results indicate the beneficial effects of prolonged α-CD/MOR supplementation that are mediated, at least in part, by Nrf2 activation. Then, α-CD/MOR could be a valuable treatment against neurodegenerative diseases, in particular motor neuron degeneration. Full article
(This article belongs to the Special Issue Role of Nrf2 in Neurodegenerative Diseases)
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Review

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18 pages, 1037 KiB  
Review
Natural Compounds That Activate the KEAP1/Nrf2 Signaling Pathway as Potential New Drugs in the Treatment of Idiopathic Parkinson’s Disease
by Sandro Huenchuguala and Juan Segura-Aguilar
Antioxidants 2024, 13(9), 1125; https://doi.org/10.3390/antiox13091125 - 18 Sep 2024
Viewed by 1121
Abstract
Recently, a single-neuron degeneration model has been proposed to understand the development of idiopathic Parkinson’s disease based on (i) the extremely slow development of the degenerative process before the onset of motor symptoms and during the progression of the disease and (ii) the [...] Read more.
Recently, a single-neuron degeneration model has been proposed to understand the development of idiopathic Parkinson’s disease based on (i) the extremely slow development of the degenerative process before the onset of motor symptoms and during the progression of the disease and (ii) the fact that it is triggered by an endogenous neurotoxin that does not have an expansive character, limiting its neurotoxic effect to single neuromelanin-containing dopaminergic neurons. It has been proposed that aminochrome is the endogenous neurotoxin that triggers the neurodegenerative process in idiopathic Parkinson’s disease by triggering mitochondrial dysfunction, oxidative stress, neuroinflammation, dysfunction of both lysosomal and proteasomal protein degradation, endoplasmic reticulum stress and formation of neurotoxic alpha-synuclein oligomers. Aminochrome is an endogenous neurotoxin that is rapidly reduced by flavoenzymes and/or forms adducts with proteins, which implies that it is impossible for it to have a propagative neurotoxic effect on neighboring neurons. Interestingly, the enzymes DT-diaphorase and glutathione transferase M2-2 prevent the neurotoxic effects of aminochrome. Natural compounds present in fruits, vegetables and other plant products have been shown to activate the KEAP1/Nrf2 signaling pathway by increasing the expression of antioxidant enzymes including DT-diaphorase and glutathione transferase. This review analyzes the possibility of searching for natural compounds that increase the expression of DT-diaphorase and glutathione transferase through activation of the KEAP1/Nrf2 signaling pathway. Full article
(This article belongs to the Special Issue Role of Nrf2 in Neurodegenerative Diseases)
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