Heterozygous CuZn superoxide dismutase deficiency produces a vascular phenotype with aging

The goal of this study was to test the hypothesis that loss of a single copy of the gene for CuZn superoxide dismutase (CuZnSOD) increases vascular superoxide levels and produces vascular dysfunction with aging. Responses of carotid arteries from young (7 months) and old (22 to 24 months of age) heterozygous CuZnSOD-deficient (CuZnSOD+/-) mice and their wild-type (CuZnSOD+/+)littermates were examined in vitro. Total superoxide dismutase activity in aorta was reduced by approximate to 30% (P < 0.05) in CuZnSOD+/- mice compared with wild-type mice. Responses to acetylcholine ( an endothelium-dependent agonist) produced relaxation that was similar (P < 0.05) in carotid arteries from young wild-type, young CuZnSOD+/-, and old wild-type mice. In contrast, relaxation to acetylcholine was markedly impaired in old CuZnSOD+/- mice (eg, 100 mu mol/L acetylcholine produced 51 +/- 5% and 96 +/- 5% relaxation in vessels from old CuZnSOD+/- and old wild-type mice, respectively). This effect was selective, because relaxation to nitroprusside (an endothelium-independent agonist) was not affected by either CuZnSOD genotype or aging. The impaired response to acetylcholine in old CuZnSOD+/- mice was restored toward normal with either tempol (a scavenger of superoxide; 1 mmol/L) or PJ34 (an inhibitor of poly-ADP-ribose polymerase; 3 mu mol/L). Vascular superoxide levels were increased in aorta in old CuZnSOD+/- mice and increased further in CuZnSOD+/- mice with aging. These findings provide the first direct evidence that normal CuZnSOD expression protects endothelial function and that deficiency in a single copy of the gene that encodes CuZnSOD produces increases in superoxide and marked impairment of endothelial function with aging.