Abstract

In our previous study, we found that pretreatment with lipoamide (LM) more effectively than alpha-lipoic acid (LA) protected retinal pigment epithelial (RPE) cells from the acrolein-induced damage. However, the reasons and mechanisms for the greater effect of LM than LA are unclear. We hypothesize that LM, rather than the more direct antioxidant LA, may act more as an indirect antioxidant. In the present study, we treated ARPE-19 cells with LA and LM and compared their effects on activation of mitochondrial biogenesis and induction of phase II enzyme systems. It is found that LM is more effective than LA on increasing mitochondrial biogenesis and inducing the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) and its translocation to the nucleus, leading to an increase in expression or activity of phase II antioxidant enzymes (NQO-1, GST, GCL, catalase and Cu/Zn SOD). Further study demonstrated that mitochondrial biogenesis and phase II enzyme induction are closely coupled via energy requirements. These results suggest that LM, compared with the direct antioxidant LA, plays its protective effect on oxidative damage more as an indirect antioxidant to simultaneously stimulate mitochondrial biogenesis and induction of phase II antioxidant enzymes.

Highlights

  • The dysfunction of retinal pigment epithelium (RPE) is strongly related to age-related macular degeneration (AMD) [1, 2]

  • Polyclonal rabbit antibodies against PPARGC1a and nuclear factor erythroid 2-related factor 2 (Nrf2) were purchased from Santa Cruz Biotechnology Inc. (San Diego, CA); monoclonal antibodies for Complex I (NADH ubiquinone oxidoreductase 39-kDa subunit), Complex II, Complex III, Complex IV and Complex V (ATP synthase, 53–kDa), were from Molecular Probes (Eugene, OR); monoclonal antibodies for GCLc, catalase and glutathione S-transferase (GST) were from Stressgen Biotechnologies Corporation (Victoria, British Columbia, Canada)

  • LM increased expression of mitochondrial electron transfer chain complexes The electron transfer chain complexes located on the inner mitochondrial membrane are essential for mitochondrial function

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Summary

Introduction

The dysfunction of retinal pigment epithelium (RPE) is strongly related to age-related macular degeneration (AMD) [1, 2]. PLOS ONE | DOI:10.1371/journal.pone.0128502 June 1, 2015

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