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G6PD hillbrow: a new variant of glucose-6-phosphate dehydrogenase associated with drug-induced haemolytic anaemia.

Abstract
A new genetic variant of the red cell enzyme glucose-6-phosphate dehydrogenase is described. It was observed in a patient presenting with severe haemolytic anaemia and renal failure following ingestion of an overdose of Beserol (paracetamol and chlormezanone). The enzyme in the red cell had 12% of the activity of a normal B+ control, but only slightly lower activity in the kidney compared with a normal control. The red cell enzyme showed normal electrophoretic mobility and thermostability, a biphasic pH optimum curve, higher than normal utilization of the substrate analogues 2-deoxy-glucose-6-phosphate and deamino-NADP, and lower than normal Michaelis constants for both substrates, glucose-6-phosphate and NADP. The enzyme was strongly inhibited in vitro by high concentrations of paracetamol and chlormezanone. The extent of inhibition was similar to that for the enzyme from a normal B+ individual.
AuthorsE Cayanis, E D Gomperts, D Balinsky, P Disler, A Myers
JournalBritish journal of haematology (Br J Haematol) Vol. 30 Issue 3 Pg. 343-50 (Jul 1975) ISSN: 0007-1048 [Print] England
PMID1201217 (Publication Type: Journal Article)
Chemical References
  • Drug Combinations
  • acetaminophen, caffeine, carisoprodol, diclofenac drug combination
  • Diclofenac
  • Carisoprodol
  • Acetaminophen
  • Caffeine
  • Glucosephosphate Dehydrogenase
  • Chlormezanone
Topics
  • Acetaminophen (pharmacology)
  • Adult
  • Anemia, Hemolytic (chemically induced)
  • Caffeine
  • Carisoprodol
  • Chlormezanone (pharmacology)
  • Diclofenac
  • Drug Combinations
  • Erythrocyte Aging (drug effects)
  • Erythrocytes (enzymology)
  • Genetic Variation
  • Glucosephosphate Dehydrogenase (antagonists & inhibitors, blood, isolation & purification)
  • Humans
  • Male

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