Simon P M, Kedinger M, Raul F, Grenier J F, Haffen K
In Vitro. 1982 Apr;18(4):339-46. doi: 10.1007/BF02796332.
Jejunal mucosa of 6 d-old rats were cultured for 24 and 48 h in the presence of thyroxine, insulin, pentagastrin, glucagon, epidermal growth factor (EGF) or dibutyryl-A-3:5-MP cyclic with or without dexamethasone (DX). The enzymes were assayed on the purified brush borders. The various agents added alone to the basic culture medium had no effect with the exception of DX on the levels of enzyme activities. Dexamethasone alone induced sucrase, stimulated maltase, and protected other brush border enzyme activities (aminopeptidase, lactase, and alkaline phosphatase). When added to DX-supplemented medium, only the following factors modified the levels of enzymatic activities observed with DX alone. Insulin (10(-6) M) increased maltase, alkaline phosphatase, and lactase activity to a greater extent than DX at 24 h culture, the effect being maintained at 48 h on alkaline phosphatase only. At 48 h culture, both EGF (10(-8) M) and dbcAMP (10(-3) M) decreased DX-induced sucrase activity. The latter agent also depressed DX-stimulated aminopeptidase activity.
将6日龄大鼠的空肠黏膜在甲状腺素、胰岛素、五肽胃泌素、胰高血糖素、表皮生长因子(EGF)或二丁酰环磷腺苷(dbcAMP)存在的情况下培养24小时和48小时,添加或不添加地塞米松(DX)。在纯化的刷状缘上测定酶活性。除DX外,单独添加到基础培养基中的各种试剂对酶活性水平没有影响。单独使用地塞米松可诱导蔗糖酶、刺激麦芽糖酶,并保护其他刷状缘酶活性(氨肽酶、乳糖酶和碱性磷酸酶)。当添加到补充了DX的培养基中时,只有以下因素改变了单独使用DX时观察到的酶活性水平。胰岛素(10^(-6)M)在培养24小时时比DX更能提高麦芽糖酶、碱性磷酸酶和乳糖酶的活性,在48小时时这种作用仅维持在碱性磷酸酶上。在培养48小时时,EGF(10^(-8)M)和dbcAMP(10^(-3)M)均降低了DX诱导的蔗糖酶活性。后一种试剂还降低了DX刺激的氨肽酶活性。