Literature DB >> 6413214

Protoporphyrinogen oxidase and ferrochelatase in porphyria variegata.

D J Viljoen, R Cummins, J Alexopoulos, S Kramer.   

Abstract

Protoporphyrinogen oxidase activity and ferrochelatase activity were measured in leucocytes from patients with porphyria variegata. The mean activity of protoporphyrinogen oxidase (PPO) in porphyria variegata (PV) was about 50% of normal (P less than 0.05). The mean activity of ferrochelatase with 59Fe2+ sulphate and protoporphyrin as substrates (in the presence of ascorbic acid) was reduced by 40% (P less than 0.009). The mean activity of ferrochelatase with 59Fe3+ chloride and protoporphyrin as substrates (in the presence of reduced glutathione) was increased by 65% (P less than 0.005). Both are statistically highly significant. The findings are interpreted as follows: (a) The occurrence of a low level of protoporphyrinogen oxidase in PV is confirmed. (b) The findings indicate a concurrent structural change in ferrochelatase (this may be structurally related to (a) but no evidence of this is at present available).

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Year:  1983        PMID: 6413214     DOI: 10.1111/j.1365-2362.1983.tb00102.x

Source DB:  PubMed          Journal:  Eur J Clin Invest        ISSN: 0014-2972            Impact factor:   4.686


  3 in total

1.  Allosteric inhibition of human lymphoblast and purified porphobilinogen deaminase by protoporphyrinogen and coproporphyrinogen. A possible mechanism for the acute attack of variegate porphyria.

Authors:  P Meissner; P Adams; R Kirsch
Journal:  J Clin Invest       Date:  1993-04       Impact factor: 14.808

2.  Mouse protoporphyrinogen oxidase. Kinetic parameters and demonstration of inhibition by bilirubin.

Authors:  G C Ferreira; H A Dailey
Journal:  Biochem J       Date:  1988-03-01       Impact factor: 3.857

Review 3.  Ferrochelatase and N-alkylated porphyrins.

Authors:  S P Cole; G S Marks
Journal:  Mol Cell Biochem       Date:  1984-09       Impact factor: 3.396

  3 in total

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