Kominami E, Tsukahara T, Bando Y, Katunuma N
Biochem Biophys Res Commun. 1987 Apr 29;144(2):749-56. doi: 10.1016/s0006-291x(87)80028-1.
Repeated injections of Ep-475, a potent cysteine proteinase inhibitor, into rats caused several-fold increase in the hepatic contents of the lysosomal cysteine proteinases cathepsin B, H and L and in the activities of other lysosomal hydrolases. The rates of degradation of these lysosomal enzymes, estimated by repeated injections of cycloheximide, were found to be retarded in Ep475-treated rats, indicating that lysosomal cysteine proteinases are involved in degradation of lysosomal enzymes including proteinases.
向大鼠反复注射一种强效半胱氨酸蛋白酶抑制剂Ep - 475,可使肝脏溶酶体半胱氨酸蛋白酶组织蛋白酶B、H和L的含量以及其他溶酶体水解酶的活性增加数倍。通过反复注射环己酰亚胺来估计这些溶酶体酶的降解速率,结果发现,在接受Ep475治疗的大鼠中,这些酶的降解速率减慢,这表明溶酶体半胱氨酸蛋白酶参与包括蛋白酶在内的溶酶体酶的降解过程。