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Effects of cyanate on the distribution of isotope-labeled H2O and extracellular markers in rat liver and tumors.

Abstract
Previous work has shown that administration of sodium cyanate inhibits the uptake of several metabolites in tumors under conditions in which there is generally no inhibition in normal tissues of the rat. In the present work, it was found that cyanate treatment inhibits the distribution of 3H2O, [3H]methoxyinulin, and [14C]sucrose in rats with greater effects in the tumors than the normal tissues examined. Tumor-bearing rats received i.p. injections of sodium cyanate (250 mg/kg body weight). After 60 min, the rats received s.c. injections of 3H2O. Treatment with cyanate decreased the radioactivity in blood and liver, but greater effects were seen in five transplanted tumors (LK1 colon tumor and Morris hepatomas 5123C, 7288CTC, 7777, and 9618A2). At 10 min after injection of 3H2O, the mean radioactivities in tumors of cyanate-treated rats were 11 to 23% of control values and in some tumors were still less than in controls at 60 min after isotope injection. Evidence was obtained that the action of cyanate was not due to osmotic effects or loss of water from the tissues. The distribution of the extracellular markers [3H]methoxyinulin and [14C]sucrose was also decreased in hepatomas in cyanate-treated rats. The data do not exclude effects on membrane permeability but suggested that cyanate decreased circulation in the tumors.
AuthorsM A Lea, J Parsons
JournalCancer research (Cancer Res) Vol. 41 Issue 12 Pt 1 Pg. 4988-92 (Dec 1981) ISSN: 0008-5472 [Print] United States
PMID7306999 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Cyanates
  • Thiocyanates
  • Water
  • Tosylphenylalanyl Chloromethyl Ketone
  • Sucrose
  • Inulin
Topics
  • Animals
  • Cyanates (pharmacology)
  • Extracellular Space (metabolism)
  • Inulin (metabolism)
  • Liver (metabolism)
  • Liver Neoplasms, Experimental (blood supply, metabolism)
  • Rats
  • Regional Blood Flow (drug effects)
  • Sucrose (metabolism)
  • Thiocyanates (pharmacology)
  • Tosylphenylalanyl Chloromethyl Ketone (pharmacology)
  • Water (metabolism)

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