Literature DB >> 7316996

Destruction of liver haem by norethindrone. Conversion into green pigments.

I N White.   

Abstract

1. Factors affecting the norethindrone-mediated conversion of hepatic haem into green pigments have been studied in the rat. Concentrations of haem and green pigments were estimated spectrophotometrically after esterification and separation by silica gel high-pressure liquid chromatography (h.p.l.c.). 2. Accumulation of green pigments in the liver was dependent on the dose of steroid and the time after dosing, maximum values being reached after 4-8h. Phenobarbitone pretreatment of rats resulted in an 8-fold increase in the concentration of green pigments at these times. 3. In microsomal systems in vitro, the formation of green pigments in the presence of NADPH and norethindrone was also dependent on the concentration of steroid and incubation times. Reaction rates very rapidly became non-linear with time, consistent with the self-catalysed destruction of the form(s) of cytochrome P-450 responsible for the metabolic activation of norethindrone. Microsomal mixtures incubated for a short period of time (1min) with norethindrone gave only one green-pigment peak after h.p.l.c. Longer incubation times gave four or five additional green pigments. Results suggested that multiple green pigments may arise by metabolic transformation of a single precursor. 4. When liver haem was prelabelled with (14)C by using 5-amino[4-(14)C]laevulinic acid, subsequent dosing with norethindrone in vivo gave rise to three major (14)C-labelled-green-pigment peaks on h.p.l.c. None of these components had the same retention times as the green pigments produced by microsomal fractions in vitro. 5. When liver haem was prelabelled with (59)Fe by using (59)FeCl(3), norethindrone administration resulted in the detection of (59)Fe-labelled green pigments if subsequent esterification was carried out under neutral conditions with trimethyloxonium tetrafluoroborate, but not when carried out under acidic conditions with methanol/H(2)SO(4). These results suggested that green pigments normally contain chelated iron and that metal-free green pigments are not produced by the liver.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7316996      PMCID: PMC1163031          DOI: 10.1042/bj1960575

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  15 in total

1.  THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. II. SOLUBILIZATION, PURIFICATION, AND PROPERTIES.

Authors:  T OMURA; R SATO
Journal:  J Biol Chem       Date:  1964-07       Impact factor: 5.157

2.  Cleavage of the haem-protein link by acid methylethylketone.

Authors:  F W TEALE
Journal:  Biochim Biophys Acta       Date:  1959-10

3.  Decreased liver cytochrome P-450 in rats caused by norethindrone or ethynyloestradiol.

Authors:  I N White; U Muller-Eberhard
Journal:  Biochem J       Date:  1977-07-15       Impact factor: 3.857

4.  Loss of haem in rat liver caused by the porphyrogenic agent 2-allyl-2-isopropylacetamide.

Authors:  F De Matteis
Journal:  Biochem J       Date:  1971-10       Impact factor: 3.857

5.  Incorporation of exogenous heme into hepatic cytochrome P-450 in vivo.

Authors:  M A Correia; G C Farrell; R Schmid; P R Ortiz de Montellano; G S Yost; B A Mico
Journal:  J Biol Chem       Date:  1979-01-10       Impact factor: 5.157

Review 6.  Increased liver haem degradation caused by foreign chemicals: a comparison of the effects of 2-allyl-2-isopropylacetamide and cobaltous chloride.

Authors:  F De Matteis; A Unseld
Journal:  Biochem Soc Trans       Date:  1976       Impact factor: 5.407

7.  Drug-induced conversion of liver haem into modified porphyrins. Evidence for two classes of products.

Authors:  F De Matteis; A H Gibbs
Journal:  Biochem J       Date:  1980-04-01       Impact factor: 3.857

8.  Self-catalyzed destruction of cytochrome P-450: covalent binding of ethynyl sterols to prosthetic heme.

Authors:  P R Ortiz de Montellano; K L Kunze; G S Yost; B A Mico
Journal:  Proc Natl Acad Sci U S A       Date:  1979-02       Impact factor: 11.205

9.  Metabolic activation of acetylenic substituents to derivatives in the rat causing the loss of hepatic cytochrome P-450 and haem.

Authors:  I N White
Journal:  Biochem J       Date:  1978-09-15       Impact factor: 3.857

10.  The effect of fluroxene [(2,2,2-trifluoroethoxy)ethane] on haem biosynthesis and degradation.

Authors:  M R Ziman; J J Bradshaw; K M Ivanetich
Journal:  Biochem J       Date:  1980-09-15       Impact factor: 3.857

View more
  6 in total

Review 1.  Acetylenes: cytochrome P450 oxidation and mechanism-based enzyme inactivation.

Authors:  Paul R Ortiz de Montellano
Journal:  Drug Metab Rev       Date:  2019-07-07       Impact factor: 4.518

2.  Factors responsible for the formation of different N-alkylated porphyrins in rat liver microsomal systems exposed to norethindrone. The role of 3 alpha-hydroxysteroid dehydrogenase.

Authors:  I N White; D C Blakey; M L Green; M Jarman; H R Schulten
Journal:  Biochem J       Date:  1986-06-01       Impact factor: 3.857

3.  Metabolic activation of acetylenes. Covalent binding of [1,2-14C]octyne to protein, DNA and haem in vitro and the protective effects of certain thiol compounds.

Authors:  I N White; J B Campbell; P B Farmer; E Bailey; N H Nam; D C Thang
Journal:  Biochem J       Date:  1984-05-15       Impact factor: 3.857

4.  Suicidal destruction of cytochrome p-450 by ethynyl substituted compounds.

Authors:  I N White
Journal:  Pharm Res       Date:  1984-07       Impact factor: 4.200

Review 5.  The association between chemical-induced porphyria and hepatic cancer.

Authors:  Andrew G Smith; John R Foster
Journal:  Toxicol Res (Camb)       Date:  2018-06-01       Impact factor: 3.524

6.  Development of methods to monitor exposure to 1-nitropyrene.

Authors:  K el-Bayoumy; B Johnson; A K Roy; P Upadhyaya; S Partian; S S Hecht
Journal:  Environ Health Perspect       Date:  1994-10       Impact factor: 9.031

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.