Literature DB >> 1148850

The action of thiamine and its di- and triphosphates on the slow exponential decline of the ionic currents in the node of Ranvier.

J M Fox, W Duppel.   

Abstract

Sodium and potassium currents in the node of Ranvier decrease exponentially with time during long lasting voltage clamp experiments. This decline is strongly dependent on temperature (Q10 approximately 3). Thiamine and, particularly, its diand triphosphoric acid esters are shown to prevent this exponential decline of the ionic currents. Thiamine acts from the outside and from the inside of the nodal membrane, but more potently from the inside. Thiamine diphosphate prevents the exponential decline of the ionic currents only when applied internally. Thiamine triphosphate, the most effective thiamine derivative was tested form the inside only. Bacterial thiaminases applied externally were not effective, presumably because they do not permeate the nodal membrane. Tetrodotoxin, that has been shown by other investigators to induce a release of thiamine from nerve membranes, does not alter the action of thiamine on the exponential decline of current and vice versa. It is concluded that: (1) thiamine diphosphate or thiamine triphosphate are the active thiamine compounds in nerve membranes; (2) the site of action is located at the internal suface of the membrane; (3) the reduction of the thiamine concentration in the membrane or in the axoplasm could cause the exponetial decline of currents; (4) the release of thiamine from nerve membranes induced by tetrodotoxin is interpreted as a side effect not even related to the mechanism by which tetrodotoxin blocks the sodium channels; (5) thiamine polyphosphates appear to stabilise the intrinsic electric field strength of the nodal membrane in the resing state. Threfore, as a working hypothesis, it is suggested that the thiamine derivatives control the number of functioning ionic channels by stabilising the density of negative surface charges at the inner side of the nerve membrane.

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Year:  1975        PMID: 1148850     DOI: 10.1016/0006-8993(75)90720-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  11 in total

1.  Remarkable electron-microscopic localization of thiamine diphosphate phosphohydrolase (TDPase) in the tanycytes of the rat.

Authors:  H Luppa; J Weiss; H G Bernstein
Journal:  Histochemistry       Date:  1976-11-12

2.  The role of thiamine in nervous tissue.

Authors:  J R Cooper; J H Pincus
Journal:  Neurochem Res       Date:  1979-04       Impact factor: 3.996

3.  Ultraviolet-induced alterations of the sodium inactivation in myelinated nerve fibres.

Authors:  W Schwarz; J M Fox
Journal:  J Membr Biol       Date:  1977-09-15       Impact factor: 1.843

4.  Morphological studies on neuroglia. V. Microglial cells in the cerebral cortex of the rat, with special reference to their possible involvement in synaptic function.

Authors:  Y Murabe; Y Sano
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

5.  Characteristics of an acid active thiamine diphosphatase from beef brain.

Authors:  J V Murphy; F E Frerman; A Hodach
Journal:  Neurochem Res       Date:  1980-02       Impact factor: 3.996

Review 6.  Thiamine in excitable tissues: reflections on a non-cofactor role.

Authors:  L Bettendorff
Journal:  Metab Brain Dis       Date:  1994-09       Impact factor: 3.584

Review 7.  Role of astrocytes in thiamine deficiency.

Authors:  Szeifoul Afadlal; Rémi Labetoulle; Alan S Hazell
Journal:  Metab Brain Dis       Date:  2014-06-15       Impact factor: 3.584

8.  Immunohistochemical demonstration of a new thiamine diphosphate-binding protein in the rat digestive tract.

Authors:  H Yoshioka; K Nishino; T Usui; M Sung; G Ohshio; T Sugiyama; T Kita
Journal:  Histochemistry       Date:  1992

9.  Thiamine as an integral component of brain synaptosomal membranes.

Authors:  T Matsuda; J R Cooper
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

10.  Thiamine triphosphate activates an anion channel of large unit conductance in neuroblastoma cells.

Authors:  L Bettendorff; H A Kolb; E Schoffeniels
Journal:  J Membr Biol       Date:  1993-12       Impact factor: 1.843

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