Hartwich G, Weisshaar K, Domschke W
Arzneimittelforschung. 1978;28(6):973-6.
Rat intestinal disaccharidase activities were investigated during treatment with different doses of 2-[bis-(2-chlorethyl)-amino]-tetrahydro-2H-1,3,2-oxazaphosphorine-2-oxide (cyclophosphamide). In all experiments, disaccharidase activities decreased--although not too drastically--within 2--3 days after beginning treatment. Loss of activity was not reversed during the period of experimentation. Contrary to previous investigations, cyclophosphamide did not exert direct toxic effects on intestinal disaccharidases. Decrease of intestinal disaccharidase activities can be interpreted to be due to cyclophosphamide effects on the proliferation cycle of epithelial crypt cells resulting in a decreased number of full-function cells.
在使用不同剂量的2-[双-(2-氯乙基)-氨基]-四氢-2H-1,3,2-恶唑磷-2-氧化物(环磷酰胺)治疗期间,对大鼠肠道双糖酶活性进行了研究。在所有实验中,双糖酶活性在开始治疗后的2至3天内下降——尽管下降幅度不算太大。在实验期间,活性丧失并未逆转。与先前的研究相反,环磷酰胺对肠道双糖酶没有直接毒性作用。肠道双糖酶活性的降低可以解释为是由于环磷酰胺对上皮隐窝细胞增殖周期的影响,导致全功能细胞数量减少。