Lazovskaia A V
Farmakol Toksikol. 1978 May-Jun;41(3):327-31.
Membranous hydrolysis of saccharose (membranous digestion) and synthesis of invertase in the intestinal epithelial cells of rats and mice following introduction of pharmacological agents were studied. Ethyl alcohol, luminal and atropine lowered both the invertased activity in the area of membranous digestion and the synthesis of the enzyime. Hexonium and pilocarpine also lowered the level of membranous hydrolysis, but not the formation of enzymes. Epinephrine and octadine, on the contrary, enhanced the intensity of both these processes. The disclosed pharmacological effects are considered in the light of features specific for the structural organization of enzymes in the area of membranous digestion.
研究了给大鼠和小鼠引入药理剂后,其肠上皮细胞中蔗糖的膜水解(膜消化)及转化酶的合成情况。乙醇、腔肠毒素和阿托品降低了膜消化区域的转化酶活性以及该酶的合成。海索那明和毛果芸香碱也降低了膜水解水平,但不影响酶的形成。相反,肾上腺素和辛卡胺增强了这两个过程的强度。根据膜消化区域酶结构组织的特定特征,对所揭示的药理作用进行了探讨。