Extracellular superoxide dismutase in tissues from obese (ob/ob) mice

被引:37
|
作者
Nakao, C
Ookawara, T
Sato, Y
Kizaki, T
Imazeki, N
Matsubara, O
Haga, S
Suzuki, K
Taniguchi, N
Ohno, H
机构
[1] Kyorin Univ, Sch Med, Dept Hyg & Prevent Med, Tokyo 1818611, Japan
[2] Nagoya Univ, Res Ctr Hlth Phys Fitness & Sports, Chikusa Ku, Aichi 4640814, Japan
[3] Hyogo Med Univ, Dept Biochem, Nishinomiya, Hyogo 6638501, Japan
[4] Natl Def Med Coll, Dept Pathol 2, Tokorozawa, Saitama 3598513, Japan
[5] Univ Tsukuba, Inst Hlth & Sport Sci, Tsukuba, Ibaragi 3050006, Japan
[6] Osaka Univ, Sch Med, Dept Biochem, Suita, Osaka 5650871, Japan
关键词
extracellular superoxide dismutase; obesity; ob/ob mouse; cytokine; affinity for heparin;
D O I
10.1080/10715760000301401
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-cc and interleukin-lp 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.
引用
收藏
页码:229 / +
页数:14
相关论文
共 50 条
  • [21] GASTROINTESTINAL APUDOSIS IN OBESE, HYPERGLYCEMIC (OB-OB) MICE
    POLAK, JM
    PEARSE, AGE
    GRIMELIUS, L
    BLOOM, SR
    MARKS, V
    JOURNAL OF ENDOCRINOLOGY, 1975, 67 (02) : P67 - P67
  • [22] CORTICOSTERONE AND TRIIODOTHYRONINE TRANSPORT INTO BRAIN OF OBESE (OB/OB) MICE
    WARWICK, B
    SUZUKI, H
    ROMSOS, DR
    INTERNATIONAL JOURNAL OF OBESITY, 1992, 16 (05) : 377 - 382
  • [23] THE MEAL PATTERN OF GENETICALLY-OBESE (OB OB) MICE
    STROHMAYER, AJ
    SMITH, GP
    APPETITE, 1987, 8 (02) : 111 - 123
  • [24] Modified control of breathing in genetically obese (ob/ob) mice
    Tankersley, C
    Kleeberger, S
    Russ, B
    Schwartz, A
    Smith, P
    JOURNAL OF APPLIED PHYSIOLOGY, 1996, 81 (02) : 716 - 723
  • [25] ENHANCED ACUTE RESPONSE TO CORTICOSTERONE BY OBESE OB/OB MICE
    TOKUYAMA, K
    HIMMSHAGEN, J
    FEDERATION PROCEEDINGS, 1987, 46 (04) : 1479 - 1479
  • [26] PANCREATIC-ISLETS OF OBESE HYPERGLYCEMIC MICE (OB/OB)
    TOMITA, T
    DOULL, V
    POLLOCK, HG
    KRIZSAN, D
    PANCREAS, 1992, 7 (03) : 367 - 375
  • [27] Leptin treatment ameliorates anxiety in ob/ob obese mice
    Asakawa, A
    Inui, A
    Inui, T
    Katsuura, G
    Fujino, MA
    Kasuga, M
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2003, 17 (02) : 105 - 107
  • [28] Reduced uptake of cholesterol by obese (OB/OB) mice macrophages
    Kjerrulf, M
    Berke, Z
    Hurt-Camejo, E
    ATHEROSCLEROSIS SUPPLEMENTS, 2004, 5 (01) : 54 - 54
  • [29] ENHANCED TUMOR RESISTANCE AND IMMUNOCOMPETENCE IN OBESE (OB/OB) MICE
    BLACK, PL
    HOLLY, M
    THOMPSON, CI
    MARGULES, DL
    LIFE SCIENCES, 1983, 33 : 715 - 718
  • [30] TEMPERATURE PREFERENCE OF GENETICALLY-OBESE (OB/OB) MICE
    CARLISLE, HJ
    DUBUC, PU
    PHYSIOLOGY & BEHAVIOR, 1984, 33 (06) : 899 - 902