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Extracellular superoxide dismutase in tissues from obese (ob/ob) mice
Authors:Chitose Nakao  Tomomi Ookawara  Yuzo Sato  Takako Kizaki  Nobuo Imazeki
Affiliation:1. Research Center of Health, Physical Fitness and Sports, Nagoya University, Furo-cho, Chikusa-Ku, Nagoya, Aichi, 464-0814, Japan;2. Department of Biochemistry, Hyogo University of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo, 663-8501, Japan;3. Department of Hygiene and Preventive Medicine, Kyorin University, School of Medicine, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan;4. Department of Pathology II, National Defense Medical College, 3-2, Namiki, Tokorozawa, Saitama, 359-8513, Japan;5. Institute of Health and Sport Sciences, University of Tsukuba, 1-1-1, Tenoudai, Tsukuba, Ibaragi, 305-0006, Japan
Abstract:
We have examined the protein content and gene expression of three superoxide dismutase (SOD) isoenzymes in eight tissues from obese ob/ob mice, particularly placing the focus on extracellular-SOD (EC-SOD) in the white adipose tissue (WAT). Obesity significantly increased EC-SOD level in liver, kidney, testis, gastrocnemius muscle, WAT, brown adipose tissue (BAT), and plasma, but significantly decreased the isoenzyme level in lung. Tumor necrosis factor-α and interleukin-1β contents in WAT were significantly higher in obese mice than in lean control mice. Immunohistochemically, both WAT and BAT from obese mice could be stained deeply with anti-mouse EC-SOD antibody compared with those from lean mice. Each primary culture per se almost time-dependently enhanced EC-SOD production, and overtly expressed its mRNA. The loss of heparin-binding affinity of EC-SOD type C with high affinity for heparin occurred in kidney of obese mice. These results suggest that the physiological importance of this SOD isoenzyme in WAT may be a compensatory adaptation to oxidative stress.
Keywords:Extracellular superoxide dismutase  obesity  ob/ob mouse  cytokine  affinity for heparin
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