Literature DB >> 5764408

The effect of cyanide on the efflux of calcium from squid axons.

M P Blaustein, A L Hodgkin.   

Abstract

1. The average rate constant for loss of (45)Ca from an unpoisoned squid axon was 1.8 x 10(-3) min(-1), corresponding to an efflux of 0.2 p-mole/cm(2) sec.2. The Ca efflux from unpoisoned axons was reduced if external calcium was replaced with magnesium, or external sodium with lithium, choline or dextrose. Replacing both sodium and calcium reduced the efflux to about 40%.3. Cyanide caused little immediate change in Ca efflux but after 1(1/2)-2(1/2) hr the efflux increased to 5-15 times its normal value. The effect was rapidly reversed when cyanide was removed.4. The large Ca efflux into cyanide was reduced by a factor of three when external calcium was replaced with magnesium and by a further factor of about six when external sodium was replaced with lithium.5. The Ca efflux from both poisoned and unpoisoned axons had a Q(10) of 2-3, was not affected by ouabain and was greatly reduced by injecting ethyleneglycol bis (aminoethylether)-N,N'-tetra-acetic acid (EGTA).6. After injecting (45)Ca along the axis, the efflux of calcium reached its maximum much more rapidly in a cyanide-treated axon than in an unpoisoned axon.7. Pre-treatment with cyanide greatly increased the rate at which calcium was lost from axoplasm extruded into flattened dialysis bags. A similar effect was observed when cyanide was applied after extrusion.8. Replacing external sodium glutamate with potassium glutamate greatly reduced the loss of (45)Ca from intact axons poisoned with cyanide but had little effect on the loss from extruded axoplasm.9. The rate constant for loss of the Ca EGTA complex was about 3 x 10(-5) min(-1) for intact axons and 2 x 10(-2) min(-1) for extruded axoplasm.10. A possible explanation of the cyanide effect is that, after poisoning, calcium ions are released from a store and can then exchange at a higher rate with external sodium or calcium.11. The experiments suggest that part of the calcium efflux may be coupled to sodium entry.12. Theoretical equations for ;diffusion and chemical reaction in a cylinder' are described in the Appendix.

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Year:  1969        PMID: 5764408      PMCID: PMC1350478          DOI: 10.1113/jphysiol.1969.sp008704

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  16 in total

1.  THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS.

Authors:  H PORTZEHL; P C CALDWELL; J C RUEEGG
Journal:  Biochim Biophys Acta       Date:  1964-05-25

2.  The effects of injecting 'energy-rich' phosphate compounds on the active transport of ions in the giant axons of Loligo.

Authors:  P C CALDWELL; A L HODGKIN; R D KEYNES; T L SHAW
Journal:  J Physiol       Date:  1960-07       Impact factor: 5.182

3.  Movements of labelled calcium in squid giant axons.

Authors:  A L HODGKIN; R D KEYNES
Journal:  J Physiol       Date:  1957-09-30       Impact factor: 5.182

4.  The intracellular calcium contents of some invertebrate nerves.

Authors:  R D KEYNES; P R LEWIS
Journal:  J Physiol       Date:  1956-11-28       Impact factor: 5.182

5.  A comparison of the phosphorus metabolism of intact squid nerve with that of the isolated axoplasm and sheath.

Authors:  P F Baker; T I Shaw
Journal:  J Physiol       Date:  1965-09       Impact factor: 5.182

6.  The dependence of calcium efflux from cardiac muscle on temperature and external ion composition.

Authors:  H Reuter; N Seitz
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

7.  ATP-dependent Ca++-extrusion from human red cells.

Authors:  H J Schatzmann
Journal:  Experientia       Date:  1966-06-15

8.  Some factors influencing sodium extrusion by internally dialyzed squid axons.

Authors:  L J Mullins; F J Brinley
Journal:  J Gen Physiol       Date:  1967-11       Impact factor: 4.086

9.  Sodium extrusion by internally dialyzed squid axons.

Authors:  F J Brinley; L J Mullins
Journal:  J Gen Physiol       Date:  1967-11       Impact factor: 4.086

10.  In vivo effect of uncoupling agents on the incorporation of calcium and strontium into mitochondria and other subcellular fractions of rat liver.

Authors:  E Carafoli
Journal:  J Gen Physiol       Date:  1967-08       Impact factor: 4.086

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  169 in total

1.  Effect of Na/Ca exchange on plateau fraction and [Ca]i in models for bursting in pancreatic beta-cells.

Authors:  D Gall; I Susa
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

2.  Roles of Na(+)-Ca2+ exchange and of mitochondria in the regulation of presynaptic Ca2+ and spontaneous glutamate release.

Authors:  A L Scotti; J Y Chatton; H Reuter
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

3.  Dependence of transient and residual calcium dynamics on action-potential patterning during neuropeptide secretion.

Authors:  M Muschol; B M Salzberg
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

4.  Responses of type I cells dissociated from the rabbit carotid body to hypoxia.

Authors:  T J Biscoe; M R Duchen
Journal:  J Physiol       Date:  1990-09       Impact factor: 5.182

5.  Evaluation of cellular mechanisms for modulation of calcium transients using a mathematical model of fura-2 Ca2+ imaging in Aplysia sensory neurons.

Authors:  H Blumenfeld; L Zablow; B Sabatini
Journal:  Biophys J       Date:  1992-10       Impact factor: 4.033

6.  The kinetics of Ca-Na exchange in excitable tissue.

Authors:  A Y Wong; J B Bassingthwaighte
Journal:  Math Biosci       Date:  1981-04       Impact factor: 2.144

7.  Kinetics of phototransduction in retinal rods of the newt Triturus cristatus.

Authors:  S Forti; A Menini; G Rispoli; V Torre
Journal:  J Physiol       Date:  1989-12       Impact factor: 5.182

8.  Calcium transport abnormality in uremic rat brain synaptosomes.

Authors:  C L Fraser; P Sarnacki; A I Arieff
Journal:  J Clin Invest       Date:  1985-11       Impact factor: 14.808

9.  Calcium entry in response to maintained depolarization of squid axons.

Authors:  P F Baker; H Meves; E B Ridgway
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

10.  Mobility and transport of magnesium in squid giant axons.

Authors:  P F Baker; A C Crawford
Journal:  J Physiol       Date:  1972-12       Impact factor: 5.182

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