Regioselective O-demethylation of scoparone: differentiation between rat liver cytochrome P-450 isozymes.

نویسندگان

  • D Müller-Enoch
  • E Büttgen
  • A Nonnenmacher
چکیده

The ratios of the scoparone O-demethylation products scopoletin to isoscopoletin were determined for reconstituted complexes of NADPH-P-450 reductase and each of four P-450 isozymes in a 2:1 molar ratio with a 1:1 mixture of [7-O-methyl-14C]- and [6-O-methyl-14C]-scoparone as substrate. The two phenobarbital inducible forms P-450PB-B and P-450PB-D have a 1:0.8 +/- 0.05 scopoletin to isoscopoletin ratio, and the two beta-naphthoflavone inducible forms P-450 beta NF-B and P-450 beta NF/ISF-G have ratios of 1:4.4 +/- 0.1 and 1:3.8 +/- 0.1, respectively. The scoparone-O-demethylation activities of the reconstituted preformed complexes of the four P-450 isozymes are given.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The activation of the cytochrome P-450 dependent monooxygenase system by light.

The cytochrome P-450 dependent monooxygenase system of rat liver microsomes is investigated by light dosimetry (action spectroscopy). The scoparone-O-demethylation activity is enhanced by light and depends on the wavelength of the irradiating light. The relative increase of the activity (about 15%) by the irradiating light (approximately 0.5 mW/cm2) is maximal at a wavelength of 400 nm. The lig...

متن کامل

Substrate specificity and alkyl group selectivity in the metabolism of N-nitrosodialkylamines.

Metabolic activation may be a key step in determining the tissue specificity of carcinogenic nitrosamines. In previous work, we characterized P450IIE1 (an acetone/ethanol-inducible form of cytochrome P-450) as the major enzyme for the metabolic activation of N-nitrosodimethylamine. In this work, we investigated the metabolism of other N-nitrosodialkylamines in rat liver microsomes and in recons...

متن کامل

Positional specificity for methyl-n-amylnitrosamine hydroxylation by cytochrome P-450 isozymes determined with monoclonal antibodies.

Inhibitory monoclonal antibodies (MAbs) were used to determine the contribution of epitope-specific cytochrome P-450 isozymes in rat liver microsomes to hydroxylation of the esophageal carcinogen methyl-n-amylnitrosamine. These P-450-catalyzed reactions form 2-, 3-, 4-, and 5-hydroxymethyl-n-amylnitrosamine, formaldehyde (demethylation), and pentaldehyde (depentylation). With uninduced microsom...

متن کامل

Metabolism of nitrosamines by purified rabbit liver cytochrome P-450 isozymes.

The metabolism of nitrosamines by microsomal cytochrome P-450 (P-450) isozymes was studied in a reconstituted monooxygenase system. P-450 LM2, LM3a, LM3b and LM3c, LM4, and LM6 were purified, respectively, from the livers of phenobarbital-treated, ethanol-treated, untreated, isosafrole-treated, and imidazole-treated rabbits. Of these isozymes, LM3a had the highest N-nitrosodimethylamine demethy...

متن کامل

Substrate Specificity and Alkyl Group Selectivity in the Metabolism of TV-Nitrosodialkylamines1

Metabolic activation may be a key step in determining the tissue specificity of carcinogenic nitrosamines. In previous work, we character ized P450IIE1 (an acetone/ethanol-inducible form of cytochrome P-450) as the major enzyme for the metabolic activation of ¿Y-nitrosodimethylamine. In this work, we investigated the metabolism of other .•V-nitrosndialkylamim-s in rat liver microsomes and in...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Zeitschrift fur Naturforschung. Section C, Biosciences

دوره 40 9-10  شماره 

صفحات  -

تاریخ انتشار 1985