Stepuro I I, Chaikovskaya N A, Solodunov A A, Artsukevich A N
Institute of Biochemistry, Academy of Sciences of Belarus.
Biochemistry (Mosc). 1997 Sep;62(9):960-6.
The oxidation of hemoglobin solutions or erythrocyte suspensions containing a mixture of deoxyHb and oxyHb by NaNO2 (under decreased partial pressure of dissolved O2) resulted in the generation of metHb and nitrosoHb. The maximum amount of nitrosoHb was generated during the oxidation of deoxyHb. An increase in oxygen content was accompanied with increased generation of metHb, which was the only hemoglobin form under aerobic conditions. In the presence of oxygen, GSH was oxidized by NaNO2 to GSSG either in solution of oxyHb or in the structure of erythrocytes. GSH decelerated the oxidation of Hb to metHb due to prolongation of the slow phase and suppression of the autocatalytic phase of the reaction. The oxidation of GSH to GSSG was induced by NO2 radicals and not by NO. The incubation of deoxyHb with S-nitrosoglutathione resulted in its complete conversion to nitrosoHb, and this indicated that NO was released during the spontaneous decomposition of GSNO. The addition of S-nitrosoglutathione to oxyHb resulted in the generation of metHb in the solution.
在溶解氧分压降低的情况下,亚硝酸钠对含有脱氧血红蛋白和氧合血红蛋白混合物的血红蛋白溶液或红细胞悬液进行氧化,会生成高铁血红蛋白和亚硝基血红蛋白。在脱氧血红蛋白氧化过程中生成的亚硝基血红蛋白量最多。氧含量增加伴随着高铁血红蛋白生成量的增加,高铁血红蛋白是有氧条件下唯一的血红蛋白形式。在有氧存在的情况下,无论是在氧合血红蛋白溶液中还是在红细胞结构中,谷胱甘肽(GSH)都会被亚硝酸钠氧化为氧化型谷胱甘肽(GSSG)。由于反应慢相的延长和自催化相的抑制,谷胱甘肽减缓了血红蛋白向高铁血红蛋白的氧化。谷胱甘肽向氧化型谷胱甘肽的氧化是由亚硝酸根自由基而非一氧化氮诱导的。脱氧血红蛋白与S - 亚硝基谷胱甘肽孵育会使其完全转化为亚硝基血红蛋白,这表明在S - 亚硝基谷胱甘肽的自发分解过程中会释放出一氧化氮。向氧合血红蛋白中添加S - 亚硝基谷胱甘肽会导致溶液中生成高铁血红蛋白。