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Wiley InterScience

Journal of Neurochemistry

Journal of Neurochemistry

Volume 103 Issue 6, Pages 2690 - 2700

Published Online: 14 Sep 2007

Journal compilation © 2010 International Society for Neurochemistry



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Hydroxytyrosol protects retinal pigment epithelial cells from acrolein-induced oxidative stress and mitochondrial dysfunction
Zhongbo Liu*,, Lijuan Sun*, Lu Zhu*,, Xu Jia*, Xuesen Li*,, Haiqun Jia*,, Ying Wang, Peter Weber, Jiangang Long§ and Jiankang Liu§
  *Institute for Nutritional Science, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences, Shanghai, China
  Graduate School of the Chinese Academy of Sciences, Beijing, China
  DSM Nutritional Products, R&D Human Nutrition and Health, Basel, Switzerland
  §Institute for Brain Aging and Dementia, University of California, Irvine, California, USA
Address correspondence and reprint requests to Jiankang Liu, PhD, Institute for Brain Aging and Dementia, University of California, 1261 Gillespie Neuroscience Research Facility, Irvine, CA 92697-4540, USA.
E-mail: j.liu@uci.edu
Copyright 2007 The Authors Journal Compilation 2007 International Society for Neurochemistry
KEYWORDS
DNA damage • hydroxytyrosol • macular degeneration • mitochondrial membrane potential • nuclear factor-E2-related factor 2 • protein carbonyl

ABSTRACT

Hydroxytyrosol (HTS) is a natural polyphenol abundant in olive oil. Increasing evidence indicates HTS has beneficial effect on human health for preventing various diseases. In the present study, we investigated the protective effects of HTS on acrolein-induced toxicity in human retinal pigment epithelial cell line, ARPE-19, a cellular model of smoking- and age-related macular degeneration. Acrolein, a major component of the gas phase cigarette smoke and also a product of lipid peroxidation in vivo, at 75 μmol/L for 24 h caused significant loss of cell viability, oxidative damage (increase in oxidant generation and oxidative damage to proteins and DNA, decrease in antioxidants and antioxidant enzymes, and also inactivation of the Keap1/Nrf2 pathway), and mitochondrial dysfunction (decrease in membrane potential, activities of mitochondrial complexes, viable mitochondria, oxygen consumption, and factors for mitochondrial biogenesis, and increase in calcium). Pre-treatment with HTS dose dependently and also time dependently protected the ARPE-19 cells from acrolein-induced oxidative damage and mitochondrial dysfunction. A short-term pre-treatment with HTS (48 h) required > 75 μmol/L for showing protection while a long-term pre-treatment (7 days) showed protective effect from 5 μmol/L on. The protective effect of HTS in this model was as potent as that of established mitochondria-targeting antioxidant nutrients. These results suggest that HTS is also a mitochondrial-targeting antioxidant nutrient and that dietary administration of HTS may be an effective measure in reducing and or preventing cigarette smoke-induced or age-related retinal pigment epithelial degeneration, such as age-associated macular degeneration.


Received July 11, 2007; revised manuscript received August 28, 2007; accepted August 28, 2007.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1471-4159.2007.04954.x About DOI

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