Literature DB >> 606245

Loss of haem from cytochrome P-450 caused by lipid peroxidation and 2-allyl-2-isoprophylacetamide. An abnormal pathway not involving production of carbon monoxide.

F De Matteis, A H Gibbs, A Unseld.   

Abstract

1. Microsomal preparations undergoing lipid peroxidation produce CO and lose haem from cytochrome P-450. 2. The amount of CO produced does not correlate with the amount of haem lost and, after pre-labelling of microsomal haem in its bridges with 5-amino[5-14C]laevulinate, the radioactivity lost from haem is not recorved as CO. 3. Similarly, when pre-labelled microsomal haem is destroyed by the action of 2-allyl-2-isopropylacetamide, no radioactivity is recovered as CO. In clear contrast, on degradation of haem by the haem oxygenase system, CO is produced in an amount equimolar to the haem lost. 4. It is concluded that (a) the CO produced during lipid peroxidation originates from a source different from haem and (b) the degradations of haem caused by lipid peroxidation and 2-allyl-2-isopropylacetamide do not involve to any significant extent evolution of the methene-bridge carbon of haem as CO.

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Year:  1977        PMID: 606245      PMCID: PMC1183788          DOI: 10.1042/bj1680417

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


  25 in total

1.  THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. I. EVIDENCE FOR ITS HEMOPROTEIN NATURE.

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

2.  CARBON MONOXIDE IN BLOOD: ANALYTICAL METHOD AND SOURCES OF ERROR.

Authors:  R F COBURN; G K DANIELSON; W S BLAKEMORE; R E FORSTER
Journal:  J Appl Physiol       Date:  1964-05       Impact factor: 3.531

3.  A new method of hemin isolation.

Authors:  R F LABBE; G NISHIDA
Journal:  Biochim Biophys Acta       Date:  1957-11

4.  180 studies of haem catabolism.

Authors:  S B Brown; R F King
Journal:  Biochem Soc Trans       Date:  1976       Impact factor: 5.407

5.  Degradation of hepatic haem to porphyrins and oxophlorins in rats treated with 2-allyl-2-isopropylacetamide.

Authors:  A F McDonagh; R Pospisil; U A Meyer
Journal:  Biochem Soc Trans       Date:  1976       Impact factor: 5.407

6.  Studies on the biosynthesis of blood pigments. I. Haem synthesis in haemolysed erythrocytes of chicken blood.

Authors:  E I DRESEL; J E FALK
Journal:  Biochem J       Date:  1954-01       Impact factor: 3.857

7.  The thiobarbituric acid reagent as a test for the oxidation of unsaturated fatty acids by various agents.

Authors:  K M WILBUR; F BERNHEIM; O W SHAPIRO
Journal:  Arch Biochem       Date:  1949-12

Review 8.  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

9.  Heme and hemoprotein catabolism during stimulation of microsomal lipid peroxidation.

Authors:  B A Schacter; H S Marver; U A Meyer
Journal:  Drug Metab Dispos       Date:  1973 Jan-Feb       Impact factor: 3.922

10.  The formation of carbon monoxide during peroxidation of microsomal lipids.

Authors:  D G Wolff
Journal:  Biochem Biophys Res Commun       Date:  1976-12-20       Impact factor: 3.575

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  9 in total

1.  Oxidative modification by low levels of HOOH can transform myoglobin to an oxidase.

Authors:  Y Osawa; K Korzekwa
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

2.  The use of proteinases to determine the topological location of cytochrome P-450 in vesicles derived from smooth endoplasmic reticulum of rat liver.

Authors:  M B Cooper; M R Estall; B R Rabin
Journal:  Biochem J       Date:  1981-05-15       Impact factor: 3.857

3.  The mechanism of haem catabolism. A study of haem breakdown in spleen microsomal fraction and in a model system by 18O labelling and metal substitution.

Authors:  R F King; S B Brown
Journal:  Biochem J       Date:  1978-07-15       Impact factor: 3.857

4.  Degradation of cytochrome P-450 haem by carbon tetrachloride and 2-allyl-2-isopropylacetamide in rat liver in vivo and in vitro. Involvement of non-carbon monoxide-forming mechanisms.

Authors:  P S Guzelian; R W Swisher
Journal:  Biochem J       Date:  1979-12-15       Impact factor: 3.857

5.  Formation of cobalt protoporphyrin in the liver of rats. A mechanism for the inhibition of liver haem biosynthesis by inorganic cobalt.

Authors:  P Sinclair; A H Gibbs; J F Sinclair; F de Matteis
Journal:  Biochem J       Date:  1979-03-15       Impact factor: 3.857

6.  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

7.  Alteration of the porphyrin nucleus of cytochrome P-450 caused in the liver by treatment with allyl-containing drugs. Is the modified porphyrin N-substituted?

Authors:  F De Matteis; L Cantoni
Journal:  Biochem J       Date:  1979-10-01       Impact factor: 3.857

8.  Degradation of endogenous hepatic heme by pathways not yielding carbon monoxide. Studies in normal rat liver and in primary hepatocyte culture.

Authors:  D M Bissell; P S Guzelian
Journal:  J Clin Invest       Date:  1980-05       Impact factor: 14.808

9.  Cimetidine induces hepatic heme oxygenase activity without altering hepatic heme catabolism.

Authors:  J Reichen; C Hoilien; G R Kirshenbaum
Journal:  Experientia       Date:  1986-08-15
  9 in total

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