Natural Products as Modulators of Nrf2 Signaling Pathway in Neuroprotection

Int J Mol Sci. 2023 Feb 13;24(4):3748. doi: 10.3390/ijms24043748.

Abstract

Neurodegenerative diseases (NDs) affect the West due to the increase in life expectancy. Nervous cells accumulate oxidative damage, which is one of the factors that triggers and accelerates neurodegeneration. However, cells have mechanisms that scavenge reactive oxygen species (ROS) and alleviate oxidative stress (OS). Many of these endogenous antioxidant systems are regulated at the gene expression level by the transcription factor Nrf2 (nuclear factor erythroid 2-related factor 2). In the presence of prooxidant conditions, Nrf2 translocates to the nucleus and induces the transcription of genes containing ARE (antioxidant response element). In recent years, there has been an increase in the study of the Nrf2 pathway and the natural products that positively regulate it to reduce oxidative damage to the nervous system, both in in vitro models with neurons and microglia subjected to stress factors and in vivo models using mainly murine models. Quercetin, curcumin, anthocyanins, tea polyphenols, and other less studied phenolic compounds such as kaempferol, hesperetin, and icariin can also modulate Nrf2 by regulating several Nrf2 upstream activators. Another group of phytochemical compounds that upregulate this pathway are terpenoids, including monoterpenes (aucubin, catapol), diterpenes (ginkgolides), triterpenes (ginsenosides), and carotenoids (astaxanthin, lycopene). This review aims to update the knowledge on the influence of secondary metabolites of health interest on the activation of the Nrf2 pathway and their potential as treatments for NDs.

Keywords: Nrf2; neurodegeneration; oxidative stress; phenolic compounds; terpenoids.

Publication types

  • Review

MeSH terms

  • Animals
  • Anthocyanins / metabolism
  • Antioxidants / pharmacology
  • Biological Products* / pharmacology
  • Mice
  • NF-E2-Related Factor 2* / drug effects
  • NF-E2-Related Factor 2* / metabolism
  • Neuroprotection* / drug effects
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects

Substances

  • Anthocyanins
  • Antioxidants
  • Biological Products
  • NF-E2-Related Factor 2
  • Reactive Oxygen Species

Grants and funding

This research received no external funding.