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J Pharmacol Exp Ther ; 363(1): 114-125, 2017 10.
Article in English | MEDLINE | ID: mdl-28790194

ABSTRACT

Nuclear factor (erythroid-derived 2)-like 2 (Nrf2) is a key regulator of oxidative stress and cellular repair and can be activated through inhibition of its cytoplasmic repressor, Kelch-like ECH-associated protein 1 (Keap1). Several small molecule disrupters of the Nrf2-Keap1 complex have recently been tested and/or approved for human therapeutic use but lack either potency or selectivity. The main goal of our work was to develop a potent, selective activator of NRF2 as protection against oxidative stress. In human bronchial epithelial cells, our Nrf2 activator, 3-(pyridin-3-ylsulfonyl)-5-(trifluoromethyl)-2H-chromen-2-one (PSTC), induced Nrf2 nuclear translocation, Nrf2-regulated gene expression, and downstream signaling events, including induction of NAD(P)H:quinone oxidoreductase 1 (NQO1) enzyme activity and heme oxygenase-1 protein expression, in an Nrf2-dependent manner. As a marker of subsequent functional activity, PSTC restored oxidant (tert-butyl hydroperoxide)-induced glutathione depletion. The compound's engagement of the Nrf2 signaling pathway translated to an in vivo setting, with induction of Nrf2-regulated gene expression and NQO1 enzyme activity, as well as restoration of oxidant (ozone)-induced glutathione depletion, occurring in the lungs of PSTC-treated rodents. Under disease conditions, PSTC engaged its target, inducing the expression of Nrf2-regulated genes in human bronchial epithelial cells derived from patients with chronic obstructive pulmonary disease, as well as in the lungs of cigarette smoke-exposed mice. Subsequent to the latter, a dose-dependent inhibition of cigarette smoke-induced pulmonary inflammation was observed. Finally, in contrast with bardoxolone methyl and sulforaphane, PSTC did not inhibit interleukin-1ß-induced nuclear factor-κB translocation or insulin-induced S6 phosphorylation in human cells, emphasizing the on-target activity of this compound. In summary, we characterize a potent, selective Nrf2 activator that offers protection against pulmonary oxidative stress in several cellular and in vivo models.


Subject(s)
Coumarins/therapeutic use , Epithelial Cells/drug effects , Lung/drug effects , NF-E2-Related Factor 2/agonists , Oxidative Stress/drug effects , Pneumonia/prevention & control , Pulmonary Disease, Chronic Obstructive/metabolism , Sulfones/therapeutic use , Animals , Blotting, Western , Cell Line , Cell Nucleus/metabolism , Coumarins/administration & dosage , Coumarins/blood , Disease Models, Animal , Drug Discovery , Epithelial Cells/metabolism , Gene Expression/drug effects , Glutathione/metabolism , HEK293 Cells , Humans , Lung/metabolism , Mice, Inbred C57BL , NAD(P)H Dehydrogenase (Quinone)/genetics , NF-E2-Related Factor 2/genetics , Ozone/toxicity , Pneumonia/etiology , Pneumonia/metabolism , Protein Transport , RNA, Small Interfering/genetics , Rats, Wistar , Smoking/adverse effects , Sulfones/administration & dosage , Sulfones/blood , Transfection
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