We have examined the protein content and gene expression of three superoxid
e dismutase (SOD) isoenzymes in eight tissues from obese ob/ob mice, partic
ularly placing the focus on extracellular-SOD (EC-SOD) in the white adipose
tissue (WAT). Obesity significantly increased EC-SOD level in liver, kidne
y, testis, gastrocnemius muscle, WAT; brown adipose tissue (BAT), and plasm
a, but significantly decreased the isoenzyme level in lung. Tumor necrosis
factor-cc and interleukin-lp contents in WAT were significantly higher in o
bese mice than in lean control mice. Immunohistochemically, both WAT and BA
T from obese mice could be stained deeply with anti-mouse EC-SOD antibody c
ompared 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 h
eparin occurred in kidney of obese mice. These results suggest that the phy
siological importance of this SOD isoenzyme in WAT may be a compensatory ad
aptation to oxidative stress.