Literature DB >> 6251380

The sodium channel and intracellular H+ blockage in squid axons.

E Wanke, E Carbone, P L Testa.   

Abstract

Sodium channels in plasma membranes can be blocked by a large variety of toxins and local anaesthetics. This property, however, is not confined to relatively large molecules. For instance, extracellularly applied small ions like hydrogen may also prevent the passive transport of permeant cations across open Na+ channels. A typical feature of this phenomenon is that the blocking action of hydrogen is gradually relieved by increasing the voltage applied across the membrane. Although in the frog skeletal muscle there is no clear evidence for a similar intracellular action, we report here for the squid giant axon remarkable effects on the ionic permeability of Na+ channels when the internal perfusate contains an excess of protons. Analysing the action of low pH inside and outside the fibre in terms of a kinetic model, we could conclude that Na+ channels in squid axons are controlled by two independent groups: one with an apparent pKa of 4.6 and the other with pKa 5.8, the former feeling one-fifth of the applied membrane potential, the latter three-quarters. As with pharmacological agents, we also show that the voltage-dependence of the H+ blockage is not affected by the presence of the inactivation gate.

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Year:  1980        PMID: 6251380     DOI: 10.1038/287062a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  13 in total

1.  Sodium channel function and the excitability of human cutaneous afferents during ischaemia.

Authors:  Cindy S-Y Lin; Julian Grosskreutz; David Burke
Journal:  J Physiol       Date:  2002-01-15       Impact factor: 5.182

2.  IK inactivation in squid axons is shifted along the voltage axis by changes in the intracellular pH.

Authors:  J R Clay
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

3.  Changes in human sensory axonal excitability induced by focal nerve compression.

Authors:  S Eric Han; Cindy S-Y Lin; Robert A Boland; Lynne E Bilston; Matthew C Kiernan
Journal:  J Physiol       Date:  2010-03-29       Impact factor: 5.182

4.  Proton block of rat brain sodium channels. Evidence for two proton binding sites and multiple occupancy.

Authors:  P Daumas; O S Andersen
Journal:  J Gen Physiol       Date:  1993-01       Impact factor: 4.086

5.  Intracellular pH and ionic channels in the Loligo vulgaris giant axon.

Authors:  E Carbone; P L Testa; E Wanke
Journal:  Biophys J       Date:  1981-08       Impact factor: 4.033

6.  Evidence for negative gating charges in Myxicola axons.

Authors:  C L Schauf
Journal:  Biophys J       Date:  1983-06       Impact factor: 4.033

7.  Pace-maker current changes during intracellular pH transients in sheep cardiac Purkinje fibres.

Authors:  P P Van Bogaert
Journal:  Pflugers Arch       Date:  1985-05       Impact factor: 3.657

8.  A novel inward-rectifying K+ current with a cell-cycle dependence governs the resting potential of mammalian neuroblastoma cells.

Authors:  A Arcangeli; L Bianchi; A Becchetti; L Faravelli; M Coronnello; E Mini; M Olivotto; E Wanke
Journal:  J Physiol       Date:  1995-12-01       Impact factor: 5.182

9.  Ungulate cardiac purkinje fibres: the influence of intracellular pH on the electrical cell-to-cell coupling.

Authors:  W R Reber; R Weingart
Journal:  J Physiol       Date:  1982-07       Impact factor: 5.182

10.  The asymmetrical effects of some ionized n-octyl derivatives on the sodium current of the giant axon of Loligo forbesi.

Authors:  J R Elliott; D A Haydon; B M Hendry
Journal:  J Physiol       Date:  1984-05       Impact factor: 5.182

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