Nakagawa Y, Hiraga K, Suga T
J Pharmacobiodyn. 1981 Oct;4(10):823-6. doi: 10.1248/bpb1978.4.823.
Oral administration of 500 mg/kg of butylated hydroxytoluene (BHT) daily for three days elevated the total glutathione (GSH) level and the activities of GSH-S-transferase for CDNB and DCNB and GSSG reductase in the rat liver. BHT-alcohol, which is a metabolite of BHT, also elevated the level or activity of these components. The induction of these components with BHT-alcohol was slightly less than that with BHT. However, BHT or BHT-alcohol in doses used had no effect on GSH peroxidase activity.
连续三天每天口服500毫克/千克的丁基羟基甲苯(BHT)可提高大鼠肝脏中的总谷胱甘肽(GSH)水平以及GSH-S-转移酶对1-氯-2,4-二硝基苯(CDNB)和2,4-二氯硝基苯(DCNB)的活性及谷胱甘肽二硫化物还原酶的活性。BHT的代谢产物BHT-乙醇也提高了这些成分的水平或活性。BHT-乙醇对这些成分的诱导作用略低于BHT。然而,所用剂量的BHT或BHT-乙醇对谷胱甘肽过氧化物酶活性没有影响。