Giannerini F, Giustarini D, Lusini L, Rossi R, Di Simplicio P
Department of Neuroscience, Pharmacology Unit, University of Siena, Via A. Moro 4, 53100, Siena, Italy.
Chem Biol Interact. 2001 Mar 14;134(1):73-85. doi: 10.1016/s0009-2797(00)00316-1.
Treatment of rats with diamide (100 mg/kg i.p.) altered the thiol components of the blood to a very different extent than in tissues (liver, kidney, lung, spleen, heart and testis). A total consumption (10 min) and regeneration (120 min) of blood glutathione (GSH), matched by a parallel increase and decrease in glutathione-protein mixed disulfides (GS-SP) was observed. In contrast, no modification of non-protein SH groups (NPSH) and protein SH groups (PSH), GS-SP and malondialdehyde (MDA) was observed in liver, kidney, lung, testis spleen and heart within same time range. In particular, only glutathione disulfide (GSSG) levels and some activities of antioxidant enzymes were modified to a small extent and in an opposite direction in some organs. For example, GSSG, and glucose-6-phosphate dehydrogenase (G-6-PDH) and catalase (CAT) activities appeared up-regulated in one tissue and down-regulated in another. The least modified organ was the liver, whereas lung and spleen were the most affected (lung, GSSG, significantly increased whereas G-6-PDH, glutaredoxin (GRX), GPX, superoxide dimutase (SOD) levels were significantly lowered; spleen, GSSG and the activity of glutathione reductase (GR), G-6-PDH and glutathione transferase (GST) were significantly decreased). The different responses of erythrocytes and organs to diamide were explained by the high affinity of hemoglobin and by the relatively high potential of thiol regeneration in organs. The rapid reversibility of the process of protein S-thiolation in blood and the small effects in organs leads us to propose the existence of an inter-organ cooperation in the rat that regulates protein S-thiolation in blood. Plasma thiols may well play a role in this process.
用二酰胺(100毫克/千克腹腔注射)处理大鼠后,血液中的硫醇成分变化程度与组织(肝脏、肾脏、肺、脾脏、心脏和睾丸)中的截然不同。观察到血液中谷胱甘肽(GSH)在10分钟内完全消耗,并在120分钟内再生,同时谷胱甘肽-蛋白质混合二硫化物(GS-SP)相应增加和减少。相比之下,在相同时间范围内,肝脏、肾脏、肺、睾丸、脾脏和心脏中的非蛋白质巯基(NPSH)、蛋白质巯基(PSH)、GS-SP和丙二醛(MDA)均未发生改变。特别是,只有谷胱甘肽二硫化物(GSSG)水平和一些抗氧化酶的活性在某些器官中受到轻微影响,且方向相反。例如,GSSG以及葡萄糖-6-磷酸脱氢酶(G-6-PDH)和过氧化氢酶(CAT)的活性在一个组织中上调,而在另一个组织中下调。受影响最小的器官是肝脏,而肺和脾脏受影响最大(肺中GSSG显著增加,而G-6-PDH、谷氧还蛋白(GRX)、谷胱甘肽过氧化物酶(GPX)、超氧化物歧化酶(SOD)水平显著降低;脾脏中GSSG以及谷胱甘肽还原酶(GR)、G-6-PDH和谷胱甘肽转移酶(GST)的活性显著降低)。红细胞和器官对二酰胺的不同反应是由于血红蛋白的高亲和力以及器官中硫醇再生的相对较高潜力。血液中蛋白质S-硫醇化过程的快速可逆性以及器官中的微小影响使我们推测大鼠体内存在一种调节血液中蛋白质S-硫醇化的器官间合作。血浆硫醇很可能在这一过程中发挥作用。