Effect of new water-soluble phenolic antioxidants on the activity of Nrf2-driven enzymes, glutathione system, and Nrf2 translocation into the nucleus
Elena B. Menshchikova1, Nikolay K. Zenkov1, Peter M. Kozhin1, Anton V. Chechushkov1, Vladislav S. Pavlov1, Lidia P. Romakh1, Marina V. Khrapova1, Anastasia E. Serykh1, Oksana B. Gritsyk1, Natalya V. Kandalintseva2
1Federal Research Center of Fundamental and Translational Medicine, Novosibirsk, Russia lemen@centercem.ru 2Novosibirsk State Pedagogical University, Novosibirsk, Russia aquaphenol@mail.ru
Keywords: reactive oxygen and nitrogen species, antioxidants, Keap1/Nrf2/ARE signaling system, NAD(P)H:quinone oxidoreductase 1, glutathione S-transferase, glutathione peroxidase, glutathione reductase, glutathione system
Abstract
Understanding the role of
reactive oxygen and nitrogen species in eustress (redox balance) and
distress (oxidative stress) development poses new challenges for
biomedical scientists and pharmacologists in the search for compounds
that can not only have a direct antioxidant (antiradical) effect, but
also affect redox-sensitive signaling pathways, primarily Keap1/Nrf2/ARE
system. Aim of the study was to investigate the influence of novel
water-soluble structurally related monophenols on key elements of
Keap1/Nrf2/ARE system induction (activity of Nrf2-driven enzymes, the
state of the glutathione system, and intracellular redistribution of
transcription factor Nrf2). Material and methods. Five original
hydrophilic structurally related monophenols, differing in the number of
tert-butyl ortho-substituents, the length of the para-alkyl
substituent, and the presence of a divalent sulfur or selenium atom in
it were investigated (phenoxane, the potassium salt of phenosan acid,
was used as a reference compound). Cell lines U937 and J774 were
cultured for 24 h in the presence of tested compounds, and comparative
analysis was performed of its ability to induce the synthesis of
Nrf2-driven enzymes of phase II xenobiotic detoxification pathway and
antioxidant enzymes (NAD(P)H: quinone oxidoreductase 1 (NQO1),
glutathione S-transferases (GST), glutathione peroxidases, glutathione
reductase (biochemical spectrophotometric methods were used to study
their activity), as well as to influence the state of glutathione system
(spectrophotometry) and translocation of transcription factor Nrf2 into
the nucleus (immunofluorescent staining, confocal microscopy) (key
events of Keap1/Nrf2/ARE signaling system activation). Results and
discussion. Monophenol TS-13 have found to be the most effective inducer
of tested enzymes in U937 cells among the structural analogs, while the
structure of the para-alkyl substituent and the degree of OH group
hindrance are important for the implementation of this effect; TS-13
also effectively enhanced Nrf2 import into J774 cell nucleus. The NQO1-
and GST-inducing abilities of structurally related monophenols are
closely interrelated, which indicates the possibility of coordinated
induction of these enzymes and the presence of a common regulatory
system that ensures their activation in response to cell treatment with
phenolic antioxidants.
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