Under oxidative stress, increased energy requirements are needed To in
duce repair mechanisms. As glucose is a major energy source in L6 myot
ubes, we evaluated glucose metabolism and transport, following exposur
e to glucose oxidase (H2O2 generating system), or xanthine oxidase (O-
2 . and H2O2 generating system), added to the medium. Exposure for 24
h to 5 mM glucose and 50 mU/ml glucose oxidase, or to 50 mu M xanthine
and 20 mU/ml xanthine oxidase resulted in significant oxidant stress
indicated by increased DNA binding activity of NF-kappa B. Under these
conditions, approximately 2-fold increase in glucose consumption, lac
tate production and CO2 release were observed. 2-deoxyglucose uptake i
nto myotubes increased time and dose dependently, reaching a 2.6 +/- 0
.4-fold and 2.2 +/- 0.7-fold after 24 h exposure to glucose oxidase an
d xanthine oxidase, respectively. Peroxidase prevented this effect, in
dicating the role of H2O2 in mediating glucose uptake activation. The
elevation in glucose uptake under oxidative stress was associated with
increased expression of GLUT1 mRNA and protein. The observed 2-deoxyg
lucose uptake activation by oxidants was not Limited to the L6 cell li
ne and was observed in 3T3-L1 adipocytes as well. (C) 1997 Elsevier Sc
ience Inc.