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Time course and inhibition of stavaroside K, veratramine and cevine-induced hemolysis by other pregnane glycosides and Veratrum alkaloids.

Abstract
Stavaroside K, veratramine and cevine induce hemolysis, whereas 7 other pregnane stavarosides and 8 Veratrum alkaloids are not hemolytic. On the other hand, erythrocytes pretreated or incubated with low concentrations of stavarosides D-F or with the 8 other Veratrum alkaloids were resistant to hemolysis induced by authentic saponin, stavaroside K, cevine or veratramine. Veratridine, zygadenine and angeloylzygadenine (the known Na-Channel-Gate toxins) revealed the most potent reduction of hemolytic activity.
AuthorsF A Badria, J D McChesney, A F Halim, A M Zaghloul, K A el Sayed
JournalDie Pharmazie (Pharmazie) Vol. 50 Issue 6 Pg. 421-3 (Jun 1995) ISSN: 0031-7144 [Print] Germany
PMID7651981 (Publication Type: Journal Article)
Chemical References
  • Cevanes
  • Glucosides
  • Pregnanes
  • Saponins
  • Veratrum Alkaloids
  • stavaroside K
  • cevine
  • veratramine
Topics
  • Cevanes (antagonists & inhibitors, pharmacology)
  • Erythrocytes (drug effects)
  • Glucosides (antagonists & inhibitors, pharmacology)
  • Hemolysis (drug effects)
  • Humans
  • In Vitro Techniques
  • Pregnanes (pharmacology)
  • Saponins (pharmacology)
  • Veratrum Alkaloids (antagonists & inhibitors, pharmacology)

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