Lebsanft J, Luippold G, Schwarz L R
Cancer Lett. 1985 Oct;29(1):29-36. doi: 10.1016/0304-3835(85)90119-3.
Drug metabolizing enzyme activities were determined in isolated putatively preneoplastic, gamma-glutamyltranspeptidase (gamma-GT) positive hepatocytes from male Wistar rats fed 2-acetylaminofluorene (AAF). The cells were isolated by affinity binding to anti-gamma-GT antibody coated dishes, the resulting suspension contained 60-87% gamma-GT-positive cells. Cytochrome P-450 dependent metabolism of benzo[a]pyrene, aldrin and ethoxyresorufin was 43-54% lower than in the parent cell suspension, glucuronidation of 3-hydroxybenzo[a]pyrene (3-OH-BP) and hydrolysis of styrene oxide were increased 1.5- and 1.4-fold, respectively. The altered pattern of drug metabolizing enzyme activities in isolated gamma-GT-positive hepatocytes is consistent with the increase in resistance of preneoplastic liver cells to hepatotoxins.
在喂食2-乙酰氨基芴(AAF)的雄性Wistar大鼠分离得到的假定癌前γ-谷氨酰转肽酶(γ-GT)阳性肝细胞中测定药物代谢酶活性。通过与包被有抗γ-GT抗体的培养皿进行亲和结合来分离细胞,所得悬浮液含有60%-87%的γ-GT阳性细胞。苯并[a]芘、艾氏剂和乙氧基试卤灵的细胞色素P-450依赖性代谢比原代细胞悬浮液低43%-54%,3-羟基苯并[a]芘(3-OH-BP)的葡萄糖醛酸化和环氧苯乙烷的水解分别增加了1.5倍和1.4倍。分离得到的γ-GT阳性肝细胞中药物代谢酶活性模式的改变与癌前肝细胞对肝毒素抗性的增加一致。