The actions of barium and strontium on exocytosis and endocytosis in the synaptic terminal of goldfish bipolar cells

J Physiol. 2001 Sep 15;535(Pt 3):809-24. doi: 10.1111/j.1469-7793.2001.t01-1-00809.x.

Abstract

1. We investigated the properties of Ca2+-sensitive steps in the cycling of synaptic vesicles by comparing the actions of Ca2+, Ba2+ and Sr2+ in the synaptic terminal of depolarizing bipolar cells isolated from the retina of goldfish. FM1-43 fluorescence and capacitance measurements demonstrated that exocytosis, endocytosis and vesicle mobilization were maintained when external Ca2+ was replaced by either Ba2+ or Sr2+. 2. The rapidly releasable pool of vesicles (RRP) was equivalent to 1.5 % of the membrane surface area when measured in the presence of 2.5 mM Ca2+, but only 0.4 % in 2.5 mM Sr2+. The relative sizes of the RRP in Ca2+, Sr2+ and Ba2+ were 1.0, 0.28 and 0.1, respectively. We conclude that a smaller proportion of docked vesicles are available for fast exocytosis triggered by the influx of Sr2+ or Ba2+ compared to Ca2+. 3. The slow phase of exocytosis was not altered when Ca2+ was replaced by Ba2+, but it was accelerated 1.6-fold in Sr2+. The peak concentrations of Ca2+, Sr2+ and Ba2+ (measured using Mag-fura-5) were approximately 4, approximately 14 and approximately 60 microM, respectively. The order of efficiency for the stimulation of slow exocytosis was Ca2+ approximately Sr2+ > Ba2+. 4. Exocytosis was prolonged after the influx of Sr2+ and Ba2+. Sr2+ was cleared from the synaptic terminal with the same time constant as Ca2+ (1.3 s), but Ba2+ was cleared 10-100 times more slowly. Although Ba(2+) stimulates the slow release of a large number of vesicles, it did so less efficiently than Ca2+ or Sr2+. 5. The recovery of the membrane capacitance was equally rapid in Sr2+ and Ca2+, demonstrating that the fast mode of endocytosis could be triggered by either cation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Barium / metabolism
  • Barium / pharmacology*
  • Calcium / metabolism
  • Electric Capacitance
  • Endocytosis / drug effects*
  • Exocytosis / drug effects*
  • Fluorescent Dyes
  • Goldfish
  • In Vitro Techniques
  • Ion Channels / drug effects
  • Neurons / drug effects
  • Neurons / metabolism*
  • Presynaptic Terminals / drug effects*
  • Pyridinium Compounds
  • Quaternary Ammonium Compounds
  • Strontium / metabolism
  • Strontium / pharmacology*
  • Synaptic Vesicles / drug effects
  • Synaptic Vesicles / metabolism

Substances

  • FM1 43
  • Fluorescent Dyes
  • Ion Channels
  • Pyridinium Compounds
  • Quaternary Ammonium Compounds
  • Barium
  • Calcium
  • Strontium