Premium
Effects of calcium and calcium‐chelating agents on the inward and outward current in the membrane of mollusc neurones
Author(s) -
Kostyuk P. G.,
Krishtal O. A.
Publication year - 1977
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1977.sp011969
Subject(s) - egta , chemistry , biophysics , calcium , intracellular , divalent , chelation , extracellular , helix pomatia , conductance , membrane potential , biochemistry , inorganic chemistry , biology , snail , ecology , mathematics , organic chemistry , combinatorics
1. Effects of internal and external Ca and Ca‐chelating agents, EGTA and EDTA on transmembrane ionic currents were studied in isolated, internally dialysed neurones from the molluscs, Helix pomatia and Limnea stagnalis . 2. The possible pharmacological effect of internally applied EGTA was investigated on the background of constant free Ca concentration (5·3 × 10 −9 M ). EGTA had no effect on Ca and Na inward currents but considerably depressed the delayed K outward current. No effective removal of this action could be achieved by the elevation of intracellular free Ca. 3. In the absence of divalent cations in the external medium, EGTA (as well as EDTA) applied either intra‐ or extracellularly caused the appearance of a very large Na inward current with kinetics similar to those of Ca inward current and with the reversal potential around 10 mV. Effective concentrations of chelating agents were 0·1 m M (extracellular) and 1·0 m M (intracellular). 4. Increase in intracellular Ca in the absence of EGTA (by dialysis of the cell with Ca‐saturated solutions) did not produce any significant effect on the delayed K outward current. The small change observed in this current could be evaluated as a depression of maximum slope conductance and a shift to more negative membrane potential. 5. Ca inward current has been found extremely sensitive to internal Ca. 5·8 × 10 −8 M of internal free Ca produced its complete depression. This effect was reversible. Na inward current could be inhibited with 3·5 × 10 −7 M intracellular Ca.