Activation of Cellular Antioxidant Defense System by Naturally Occurring Dibenzopyrone Derivatives Confers Neuroprotection against Oxidative Insults

ACS Chem Neurosci. 2021 Aug 4;12(15):2798-2809. doi: 10.1021/acschemneuro.1c00023. Epub 2021 Jul 23.

Abstract

Seven dibenzopyrone phenolic derivatives, i.e., alternariol (1), alternariol 5-O-methyl ether (2), altenusin B (3), dehydroaltenusin (4), altenuene (5), altenusin (6), and alterlactone (7), were isolated from endophytic fungi Alternaria alternata extract, and these compounds' structures were elucidated based on various spectroscopic data. Compound 3, a diphenic acid derivative, was determined as a new compound. In this study, compounds 3, 4, 6, and 7 displayed remarkable neuroprotective effects against oxidative injuries by acting as potent activators of nuclear factor-erythroid derived 2-like 2 (Nrf2) in PC12 cells. A mechanistic study indicated that these compounds induced the nuclear accumulation of Nrf2, promoted the expression of Nrf2-governed cytoprotective genes, and increased the cellular antioxidant capacity. More importantly, genetic silence of Nrf2 expression deprived the observed cytoprotection, highlighting the important role of Nrf2 in the protection of these compounds.

Keywords: Nrf2; antioxidant; dibenzopyrone derivatives; neuroprotective effect; oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternaria
  • Animals
  • Antioxidants* / pharmacology
  • NF-E2-Related Factor 2 / metabolism
  • Neuroprotection*
  • Oxidative Stress
  • PC12 Cells
  • Rats

Substances

  • Antioxidants
  • NF-E2-Related Factor 2

Supplementary concepts

  • Alternaria alternata