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Departments of 1 Endocrinology and 2 Anesthesiology, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Increased production of
oxygen free radicals is an important mechanism of endothelial
dysfunction in diabetes mellitus. Our goal was to test whether
adenovirus (Ad)-mediated gene transfer of copper/zinc (CuZn) or
manganese superoxide dismutase (Mn SOD) improves relaxation of diabetic
vessels. The aortas from 9 alloxan-induced diabetic mellitus (DM) and
16 control rabbits were used. Control and DM rings were transduced ex
vivo with Ad vectors encoding Mn SOD (AdMn SOD), CuZn SOD (AdCuZn SOD),
-galactosidase (Ad
gal), or diluents. In the absence of gene
transfer, SOD activity was significantly increased in DM aortas.
Transgene expression in DM AdCuZn SOD and DM AdMn SOD-transduced
vessels was confirmed by Western blot analysis and by increased SOD
activity (DM AdCuZn SOD, 76.2 ± 9.3; DM AdMn SOD, 65.2 ± 4.8; P < 0.05 vs. DM Ad
gal; 50.9 ± 4.4 U/mg protein). Superoxide production was increased in DM
Ad
gal-transduced aorta and relaxations to acetylcholine were
impaired in these vessels. Gene transfer of CuZn SOD and Mn SOD
corrected both of these defects. Thus Ad-mediated gene transfer CuZn
and Mn SOD to the diabetic aorta improves endothelium-dependent relaxation.
adenoviral vector; endothelium; diabetes mellitus
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