Isaacs J T, Binkley F
Biochim Biophys Acta. 1977 Jun 23;498(1):29-38. doi: 10.1016/0304-4165(77)90084-8.
The disulfide-sulfhydryl ratio of rat hepatic tissue has been found to vary diurnally lowest in the early morning and highest in the early evening (Isaacs, J. (1976) Fed. Proc. 35, 1472, and Isaacs, J. and Binkley, F. (1977) Biochim. Biophys. Acta 497, 192-204). Intraperitoneal injections of dibutyryl cyclic AMP induces an increase in hepatic glutathione protein mixed disulfides (GSSProt) combined with a corresponding decrease in reduced glutathione (GSH) and protein sulfhydryl (ProtSH). Also, dibutyryl cyclic AMP caused hepatic catalase activity to decrease and to increase hepatic production of peroxide molecules. A decrease in catalase activity directs more of the increased peroxide into the glutathione peroxidase pathway. This leads to increased amounts of oxidized glutathione (GSSG) which ultimately results in increased levels of GSSProt. Therefore cyclic AMP may mediate its effect on the disulfide-sulfhydryl ratio via control over catalase and peroxide generation. Support for this idea is provided by the close temporal correlation between the diurnal variations in cyclic AMP, hepatic catalase, peroxide generation and GSSProt-GSH levels.
已发现大鼠肝脏组织中二硫键与巯基的比例存在昼夜变化,清晨最低,傍晚最高(艾萨克斯,J.(1976年)《联邦程序》35卷,第1472页;以及艾萨克斯,J.和宾克利,F.(1977年)《生物化学与生物物理学学报》497卷,第192 - 204页)。腹腔注射二丁酰环磷腺苷可导致肝脏谷胱甘肽蛋白混合二硫键(GSSProt)增加,同时还原型谷胱甘肽(GSH)和蛋白巯基(ProtSH)相应减少。此外,二丁酰环磷腺苷会使肝脏过氧化氢酶活性降低,并增加肝脏过氧化物分子的生成。过氧化氢酶活性降低会使更多增加的过氧化物进入谷胱甘肽过氧化物酶途径。这会导致氧化型谷胱甘肽(GSSG)量增加,最终导致GSSProt水平升高。因此,环磷腺苷可能通过控制过氧化氢酶和过氧化物生成来介导其对二硫键与巯基比例的影响。环磷腺苷、肝脏过氧化氢酶、过氧化物生成以及GSSProt - GSH水平的昼夜变化之间的紧密时间相关性为这一观点提供了支持。