Effect of Thiol Status on Nitric Oxide Metabolism in the Circulation

To elucidate the dynamics of nitric oxide (NO) metabolism in the circulation and its relationship with glutathione metabolism, formation of nitrosylhemoglobin (NO–Hb),S-nitrosothiols (RSNO), and nitrite + nitrate (NOx) was determined in blood samples from normal rats and animals that were treated with a loading dose of GSH orl-buthionine-[S,R]-sulfoximine (BSO), a specific inhibitor of GSH synthesis. When incubatedin vitrowith 0.2 mmNOC7, an NO donor, NO–Hb levels increased rapidly, peaked at 10 min, and decreased thereafter with a half-life of 35 min in blood samples from control, BSO-treated, or GSH-loaded animals. Levels of low-molecular-weight RSNO in plasma samples from the three animal groups also increased transiently, peaked at 10 min, and decreased thereafter. However, the amount of RSNO formed in GSH-loaded rat plasma was significantly greater than in control and BSO-treated animals. Plasma levels of NOx rapidly and similarly increased in all animal groups. Intravenously injected NOC7 also generated NO–Hb in circulating erythrocytes. In control animals, blood levels of NO–Hb increased maximally at 30 min and decreased thereafter with a half-life of 100 min. NO–Hb formed in the GSH-loaded group was significantly lower than in the control group. In contrast, the rate of NO–Hb formation was significantly higher with the BSO-treated group than with the control group. Although NOC7 did not affect the plasma levels of low-molecular-weight RSNO in plasma of both control and BSO-treated groups, it significantly increased RSNO in the GSH-loaded group. Thirty minutes after administration of NOC7, about 20% of the dose was recovered as plasma NOx in all animal groups. These results suggested that GSH status in animals might affect the metabolism of NO.