Tetronothiodin, a novel cholecystokinin type-B receptor antagonist produced by Streptomyces sp. NR0489. II. Isolation, characterization and biological activities

J Antibiot (Tokyo). 1993 Jan;46(1):11-7. doi: 10.7164/antibiotics.46.11.

Abstract

A novel cholecystokinin type-B receptor antagonist named tetronothiodin has been isolated by column chromatography and preparative HPLC from the fermentation broth of Streptomyces sp. NR0489. Tetronothiodin inhibited the binding of CCK8 (C-terminal octapeptide of cholecystokinin) to rat cerebral cortex membranes (CCK type-B receptors) with an IC50 of 3.6 nM, whereas it did not inhibit CCK8 binding to rat pancreatic membranes (CCK type-A receptors). It also inhibited CCK8 induced Ca2+ mobilization in GH3 cells, a rat anterior pituitary cell line, but was without effect on the basal cytosolic Ca2+ concentration. This finding indicated tetronothiodin was an antagonist of CCK type-B receptors.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Line
  • Cerebral Cortex / drug effects
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid
  • Furans / chemistry*
  • Furans / isolation & purification
  • Furans / pharmacology
  • Magnetic Resonance Spectroscopy
  • Pancreas / drug effects
  • Pituitary Gland, Anterior / drug effects
  • Rats
  • Receptors, Cholecystokinin / antagonists & inhibitors*
  • Sincalide / antagonists & inhibitors
  • Streptococcus / chemistry*
  • Thiophenes / chemistry*
  • Thiophenes / isolation & purification
  • Thiophenes / pharmacology

Substances

  • Furans
  • Receptors, Cholecystokinin
  • Thiophenes
  • tetronothiodin
  • Sincalide
  • Calcium