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Astaxanthin protects mitochondrial redox state and functional integrity against oxidative stress
Authors:Alexander M Wolf  Sadamitsu Asoh  Hidenori Hiranuma  Ikuroh Ohsawa  Kumiko Iio  Akira Satou  Masaharu Ishikura  Shigeo Ohta
Institution:1. Department of Biochemistry and Cell Biology, Institute of Development and Aging Sciences, Nippon Medical School, Nakahara-ku, Kawasaki, Kanagawa 211-8533, Japan;2. The Center of Molecular Hydrogen Medicine, Institute of Development and Aging Sciences, Nippon Medical School, 1-396 Kosugi-cho, Nakahara-ku, Kawasaki, Kanagawa 211-8533, Japan;3. Life Science Institute, Yamaha Motor Co. Ltd., 3001-10 Kuno, Fukuroi, Shizuoka 437-0061, Japan;1. Center for Cancer Prevention Research, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA;2. Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA;3. School of Pharmacy, China Pharmaceutical University, Nanjing 211198, People’s Republic of China;4. Graduate Program in Pharmaceutical Sciences, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA;1. Department of Ophthalmology and Visual Sciences, University of Utah, 65 N Mario Capecchi Dr, Salt Lake City, UT, United States;2. Department of Neurobiology and Anatomy, University of Utah, 20 S 2030 E, Salt Lake City, UT, United States;1. Equine Breeding Science Division, Hidaka Training and Research Center, Japan Racing Association, Urakawa, Hokkaido, Japan;2. Medical Nutrition Division, Department of Research and Development, AstaReal Co. Ltd., Chuo-ku, Osaka, Japan
Abstract:Mitochondria combine the production of energy with an efficient chain of reduction–oxidation (redox) reactions but also with the unavoidable production of reactive oxygen species. Oxidative stress leading to mitochondrial dysfunction is a critical factor in many diseases, such as cancer and neurodegenerative and lifestyle-related diseases. Effective antioxidants thus offer great therapeutic and preventive promise. Investigating the efficacy of antioxidants, we found that a carotenoid, astaxanthin (AX), decreased physiologically occurring oxidative stress and protected cultured cells against strong oxidative stress induced with a respiratory inhibitor. Moreover, AX improved maintenance of a high mitochondrial membrane potential and stimulated respiration. Investigating how AX stimulates and interacts with mitochondria, a redox-sensitive fluorescent protein (roGFP1) was stably expressed in the cytosol and mitochondrial matrix to measure the redox state in the respective compartments. AX at nanomolar concentrations was effective in maintaining mitochondria in a reduced state. Additionally, AX improved the ability of mitochondria to remain in a reduced state under oxidative challenge. Taken together, these results suggest that AX is effective in improving mitochondrial function through retaining mitochondria in the reduced state.
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