Ozeki T, Tokawa Y, Ogasawara T, Kubota Y, Takenaka K
Clin Chim Acta. 1976 Sep 20;71(3):363-70. doi: 10.1016/0009-8981(76)90086-3.
The enzyme liberated by some treatments and the changes in arylsulfatase C activity in chronic hepatic damage were investigated in rat liver. 1. The enzyme activity liberated by ultrasound was the highest in the conditions studied. 2. Arylsulfatase C was assayed using p-nitrophenyl sulfate in 0.25 M Tris/acetate buffer as substrate. It is shown that this method can be used to measure arylsulfatase C activity in a mixture of arylsulfatases A and B. 3. The enzyme is mainly located in the microsomal fraction in rat liver. In toxic hepatic damage, the enzyme activity decreases from the early stage; decreasing markedly in chronic hepatic damage. The activity seems to reflect damage to the microsomes and therefore arylsulfatase C activity can be a good indicator of injury to liver microsomes.
在大鼠肝脏中研究了某些处理所释放的酶以及慢性肝损伤中芳基硫酸酯酶C活性的变化。1.在所研究的条件下,超声释放的酶活性最高。2.使用对硝基苯硫酸酯在0.25M Tris/醋酸盐缓冲液中作为底物测定芳基硫酸酯酶C。结果表明,该方法可用于测定芳基硫酸酯酶A和B混合物中的芳基硫酸酯酶C活性。3.该酶主要位于大鼠肝脏的微粒体部分。在中毒性肝损伤中,酶活性从早期就开始下降;在慢性肝损伤中显著下降。该活性似乎反映了微粒体的损伤,因此芳基硫酸酯酶C活性可以作为肝微粒体损伤的良好指标。