Collaborative Power of Nrf2 and PPAR γ Activators against Metabolic and Drug-Induced Oxidative Injury

Abstract

Mammalian cells have evolved a unique strategy to protect themselves against oxidative damage induced by reactive oxygen species (ROS). Especially, two transcription factors, nuclear factor erythroid 2p45-related factor 2 (Nrf2) and peroxisome proliferator-activated receptor γ (PPARγ), have been shown to play key roles in establishing this cellular antioxidative defense system. Recently, several researchers reported ameliorating effects of pharmacological activators for these Nrf2 and PPARγ pathways on the progression of various metabolic disorders and drug-induced organ injuries by oxidative stress. In this review, general features of Nrf2 and PPARγ pathways in the context of oxidative protection will be summarized first. Then, a number of successful applications of natural and synthetic Nrf2 and PPARγ activators to the alleviation of pathological and drug-related oxidative damage will be discussed later.

Figure 1

Crosstalk between Nrf2 and PPARγ pathways against oxidative stress. Abbreviations used within the figure are as follows. Nrf2; nuclear factor erythroid 2-related factor 2, KEAP1; Kelch-like ECH-associated protein 1, CUL3; cullin3, PPARγ; peroxisome proliferator-activated receptor γ, HO-1; heme oxygenase-1, NQO-1; NAD(P)H quinone oxidoreductase-1, GST; glutathione, γ-GCL; γ-glutamyl cysteine ligase, SOD; superoxide dismutase, CAT; catalase, GPX; glutathione peroxidase, AREs; anti-oxidant response elements, MnSOD; manganese superoxide dismutase, PPREs; PPAR response element, RXR; retinoid X receptor.