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Effect of bathocuproine disulfonate, a copper chelator, on cyst(e)ine metabolism by freshly isolated rat hepatocytes.

Abstract
The metabolism of L-cysteine was studied in freshly isolated rat hepatocytes. Because cysteine is rapidly oxidized in oxygenated incubation medium at neutral pH, the effect of bathocuproine disulfonate, a copper-specific chelator, was investigated. Addition of bathocuproine disulfonate resulted in a higher extracellular cysteine-to-half-cystine ratio in incubations of hepatocytes with cysteine. Bathocuproine disulfonate also increased the total uptake and metabolism of cysteine plus cystine [cyst(e)ine] by hepatocytes, which is consistent with the more efficient transport of cysteine than of cystine by freshly isolated rat hepatocytes. The partitioning of cysteine between cysteinesulfinate-dependent and cysteinesulfinate-independent pathways of catabolism was also altered by the addition of bathocuproine disulfonate; the percentage of total catabolic flux that resulted in taurine plus hypotaurine formation was greater, and the percentage of total catabolic flux that occurred by the beta-cleavage of cystine in a reaction catalyzed by gamma-cystathionase was less in incubations that contained bathocuproine disulfonate. Thus addition of bathocuproine disulfonate to maintain a higher extracellular thiol-to-disulfide ratio favored cysteinesulfinate-dependent catabolism of cysteine in rat hepatocytes.
AuthorsR M Coloso, M R Drake, M H Stipanuk
JournalThe American journal of physiology (Am J Physiol) Vol. 259 Issue 3 Pt 1 Pg. E443-50 (Sep 1990) ISSN: 0002-9513 [Print] United States
PMID2399977 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Alkynes
  • Chelating Agents
  • Phenanthrolines
  • Cystine
  • propargylglycine
  • bathocuproine sulfonate
  • Copper
  • Pargyline
  • Cysteine
  • Glycine
Topics
  • Alkynes
  • Animals
  • Cells, Cultured
  • Chelating Agents (pharmacology)
  • Copper (metabolism)
  • Cysteine (metabolism, pharmacology)
  • Cystine (metabolism, pharmacology)
  • Glycine (analogs & derivatives, pharmacology)
  • Kinetics
  • Liver (drug effects, metabolism)
  • Male
  • Models, Biological
  • Pargyline (analogs & derivatives, pharmacology)
  • Phenanthrolines (pharmacology)
  • Rats
  • Rats, Inbred Strains

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