首页> 外文OA文献 >Time Course of Induction of Cytochrome P-450, NADPH-Cytochrome c Reductase, and Cinnamic Acid Hydroxylase by Phenobarbital, Ethanol, Herbicides, and Manganese in Higher Plant Microsomes 1
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Time Course of Induction of Cytochrome P-450, NADPH-Cytochrome c Reductase, and Cinnamic Acid Hydroxylase by Phenobarbital, Ethanol, Herbicides, and Manganese in Higher Plant Microsomes 1

机译:苯巴比妥,乙醇,除草剂和锰在高等植物微粒体中诱导细胞色素P-450,NADPH-细胞色素c还原酶和肉桂酸羟化酶的时程1

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摘要

The mixed function oxidase trans-cinnamic acid 4-hydroxylase, cytochrome P-450, cytochrome b5, and NADPH-cytochrome c (P-450) reductase were measured in microsomes from aging artichoke tuber slices exposed to manganese, ethanol, phenobarbital, and the herbicides Chloro-IPC, Dichlobenil, and Monuron. Although the microsomal hydroxylating complex is already induced by the slicing and aging process, 25 millimolar MnCl2, 4 millimolar phenobarbital, and 300 millimolar ethanol caused a marked increase of hydroxylase activity and cytochrome P-450 content and shifted their time course. The herbicides, 200 micromolar Dichlobenil and 200 micromolar Monuron, were less effective. Chloro-IPC was slightly inhibitory. NADPH cytochrome c reductase was significantly increased only in phenobarbital-treated slices. Cytochrome b5 was generally the least affected among the parameters being measured. The mechanisms by which these compounds increase cytochrome P-450 content and hydroxylase activity are not yet defined.
机译:在暴露于锰,乙醇,苯巴比妥和维生素B的老化朝鲜蓟块茎切片的微粒体中测量了混合功能氧化酶反式肉桂酸4-羟化酶,细胞色素P-450,细胞色素b5和NADPH-细胞色素c(P-450)还原酶。除草剂Chloro-IPC,Dichlobenil和Monuron。尽管切片和老化过程已经诱导了微粒体羟化复合物,但是25毫摩尔MnCl2、4毫摩尔苯巴比妥和300毫摩尔乙醇引起羟化酶活性和细胞色素P-450含量的显着增加,并改变了它们的时间进程。除草剂200微摩尔的地克非尼和200微摩尔的Monuron,效果较差。 Chloro-IPC具有轻微的抑制作用。 NADPH细胞色素c还原酶仅在苯巴比妥治疗的切片中显着增加。细胞色素b5通常在所测参数中受影响最小。这些化合物增加细胞色素P-450含量和羟化酶活性的机制尚未确定。

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