Literature DB >> 5653884

On the electrogenic sodium pump in mammalian non-myelinated nerve fibres and its activation by various external cations.

H P Rang, J M Ritchie.   

Abstract

1. A study has been made of the hyperpolarization that follows a period of electrical activity (the post-tetanic hyperpolarization) in mammalian non-myelinated nerve fibres.2. Evidence is presented that under certain circumstances this postetanic hyperpolarization is a result of activity of an electrogenic sodium pump that normally is absolutely dependent on the external presence of potassium.3. When the external chloride is replaced by sulphate or by isethionate the post-tetanic hyperpolarization, which in normal Locke solution is only a few millivolts in amplitude, is increased usually to about 20 mV, and on occasion to 35 mV.4. This effect of removing the chloride takes several minutes to develop and is consistent with the idea that the increase in the post-tetanic response is the result of removing the short-circuiting effect of internal chloride ions (by their being washed out into the chloride-free bathing medium).5. Small anions, such as chloride, nitrate, iodide, bromide, and thiocyanate can short-circuit the electrogenic pump, whereas larger anions such as sulphate and isethionate cannot. The bicarbonate ion, which is larger than chloride, short-circuits the pump but less effectively.6. In Locke solution containing 5 mM potassium the post-tetanic hyperpolarization declines exponentially, with a time constant of about 1-3 min. The time constant is inversely related to the external potassium concentration.7. However, when the external potassium concentration is zero the hyperpolarization declines rapidly to a very small value. Subsequent addition of potassium to the bathing medium causes a marked redevelopment of the hyperpolarization.8. This potassium-activated response declines exponentially with a time constant that is inversely related to the potassium concentration. When the added potassium concentration is 5 mM, the time constant is 1.9 min.9. The amplitude of the potassium-activated response increases with increasing concentrations of potassium.10. Other cations can produce this activated response. Thus, thallium is more effective than, rubidium as effective as, caesium and ammonium about 1/10 as effective as, and lithium ions about 1/30 as effective as potassium in producing the activated response. Choline is quite ineffective.11. The size of the post-tetanic response is little affected by changes in the duration of the period of stimulation. However, increasing the duration definitely increases the time constant of recovery.12. Reducing the external sodium concentration increases the size of the post-tetanic hyperpolarization (by about 25%), but the effect is complex and requires further study.13. Reducing the calcium of the Locke-solution from 2.2 to 0.2 mM has no appreciable effect on the post-tetanic response, nor has increasing the pH of the Locke from 7.2 to 9.2.14. When the membrane potential is increased or decreased, by externally applied currents, there is relatively little change in the post-tetanic response.15. A mathematical model of the electrogenic pump, devised to mimic the experimental results, was analysed with an analogue computer. A satisfactory agreement between model and experiment was achieved by a model in which: (1) the rate of extrusion of sodium ions depends on the degree to which a pool of carrier molecules on the inside surface of the membrane is combined with sodium; (2) each carrier molecule transfers three sodium ions at a time; (3) the rate constant for extrusion of sodium ions also depends on the presence externally of potassium ions, which combine with some sites on the external surface of the membrane that are half-saturated when the external concentration of potassium is 2.8 mM.

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Year:  1968        PMID: 5653884      PMCID: PMC1351742          DOI: 10.1113/jphysiol.1968.sp008502

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


  32 in total

1.  AN ELECTROGENIC SODIUM PUMP IN SNAIL NERVE CELLS.

Authors:  G A KERKUT; R C THOMAS
Journal:  Comp Biochem Physiol       Date:  1965-01

2.  SOME FURTHER OBSERVATIONS ON THE SODIUM EFFLUX IN FROG MUSCLE.

Authors:  R D KEYNES
Journal:  J Physiol       Date:  1965-05       Impact factor: 5.182

3.  Effects of pH, changes in potassium concentration and metabolic inhibitors on the after-potentials of mammalian non-medullated nerve fibres.

Authors:  O HOLMES
Journal:  Arch Int Physiol Biochim       Date:  1962-03

4.  The action of acetylcholine on conduction in mammalian non-myelinated fibres and its prevention by an anticholinesterase.

Authors:  C J ARMETT; J M RITCHIE
Journal:  J Physiol       Date:  1960-06       Impact factor: 5.182

5.  Membrane potential changes during sodium transport in frog sartorius muscle.

Authors:  R P KERNAN
Journal:  Nature       Date:  1962-03-10       Impact factor: 49.962

6.  On the permeability of mammalian non-myelinated fibres to sodium and to lithium ions.

Authors:  C J Armett; J M Ritchie
Journal:  J Physiol       Date:  1963-01       Impact factor: 5.182

7.  Post-tetanic hyperpolarization and electrogenic Na pump in stretch receptor neurone of crayfish.

Authors:  S Nakajima; K Takahashi
Journal:  J Physiol       Date:  1966-11       Impact factor: 5.182

8.  The dependence on external cations of the oxygen consumption of mammalian non-myelinated fibres at rest and during activity.

Authors:  H P Rang; J M Ritchie
Journal:  J Physiol       Date:  1968-05       Impact factor: 5.182

9.  The origin of the initial heat associated with a single impulse in mammalian non-myelinated nerve fibres.

Authors:  J V Howarth; R D Keynes; J M Ritchie
Journal:  J Physiol       Date:  1968-02       Impact factor: 5.182

10.  The concentration dependence of sodium efflux from muscle.

Authors:  L J MULLINS; A S FRUMENTO
Journal:  J Gen Physiol       Date:  1963-03       Impact factor: 4.086

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  165 in total

1.  Time course of post-excitatory effects separates afferent human C fibre classes.

Authors:  C Weidner; R Schmidt; M Schmelz; M Hilliges; H O Handwerker; H E Torebjörk
Journal:  J Physiol       Date:  2000-08-15       Impact factor: 5.182

2.  Extracellular potassium activity, intracellular and extracellular potential responses in the spinal cord.

Authors:  E W Lothman; G G Somjen
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

3.  Proceedings: Osmoreception and thirst in the dog.

Authors:  D J Ramsay; J B Rolls; R J Wood
Journal:  J Physiol       Date:  1975-11       Impact factor: 5.182

4.  A comparison of radioactive thallium and potassium fluxes in the giant axon of the squid.

Authors:  D Landowne
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

5.  Stimulation-induced factors which affect augmentation and potentiation of trasmitter release at the neuromuscular junction.

Authors:  K L Magleby; J E Zengel
Journal:  J Physiol       Date:  1976-09       Impact factor: 5.182

6.  Contribution of an electrogenic sodium pump to the membrane potential in rabbit sinoatrial node cells.

Authors:  A Noma; H Irisawa
Journal:  Pflugers Arch       Date:  1975-08-12       Impact factor: 3.657

7.  Contribution of an electrogenic sodium pump to membrane potential in mammalian skeletal muscle fibres.

Authors:  N Akaike
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

8.  Extra spike formation in sensory neurons and the disruption of afferent spike patterning.

Authors:  Ron Amir; Marshall Devor
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

9.  Inhibition of SERCA2 Ca(2+)-ATPases by Cs(+).

Authors:  Gary J Kargacin; Roozbeh Aschar-Sobbi; Margaret E Kargacin
Journal:  Pflugers Arch       Date:  2004-10-12       Impact factor: 3.657

10.  Some further observations on the electrogenic sodium pump in non-myelinated nerve fibres.

Authors:  A den Hertog
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

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