de Toranzo E G, Marzi A, Castro J A
Toxicology. 1981;19(1):77-82. doi: 10.1016/0300-483x(81)90067-6.
Cystamine and cysteine inhibited the carbon tetrachloride (CCl4) prooxidant effect on rat liver microsomal preparations, at concentrations ranging from 0.001 mM to 1 mM. Cysteine exhibited a biphasic effect being an inhibitor of the prooxidant action at concentrations below 0.1 mM and acting as an enhancer at 1 mM. Cystamine but not cysteine pretreatment of the rats prevented the CCl4 induced decrease in the arachidonic acid content of liver microsomal phospholipids. However, both cystamine and cysteine led to decreases in arachidonic acid similar to that produced by CCl4 but they do not have deleterious effects on the liver. These results cast doubt on the role of lipid peroxidation in the liver cell injury by CCl4.
半胱胺和半胱氨酸在0.001 mM至1 mM的浓度范围内,可抑制四氯化碳(CCl4)对大鼠肝微粒体制剂的促氧化作用。半胱氨酸呈现双相效应,在浓度低于0.1 mM时是促氧化作用的抑制剂,而在1 mM时则起增强剂的作用。对大鼠进行半胱胺而非半胱氨酸预处理,可防止CCl4诱导的肝微粒体磷脂中花生四烯酸含量的降低。然而,半胱胺和半胱氨酸都会导致花生四烯酸含量下降,类似于CCl4所产生的情况,但它们对肝脏没有有害影响。这些结果使人对脂质过氧化在CCl4所致肝细胞损伤中的作用产生怀疑。