Literature DB >> 2430631

Effects of some chemical reagents on sodium current inactivation in myelinated nerve fibers of the frog.

M Rack, N Rubly, C Waschow.   

Abstract

The effect of several chemical reagents on the sodium current was studied in voltage-clamped single nerve fibers of the frog. The oxidants halazone and hypochlorous acid drastically inhibited inactivation. Their effect was similar to that of chloramine T (Wang, 1984a). The curve relating the steady-state inactivation parameter h infinity to the conditioning potential E became nonmonotonic after treatment with the oxidants, i.e., dh infinity/dE greater than 0 for E greater than -20 mV. By contrast, the oxidants periodate, iodate, and hydrogen peroxide (applied for the same time, but at higher concentrations) merely produced a parallel shift of the h infinity(E) curve to more negative values of membrane potential. Diethylpyrocarbonate, a reagent that preferentially modifies histidine groups, had one marked effect: a strong shift of the h infinity(E) curve to more negative values of membrane potential. Almost no effect was observed after application of the tyrosine-reactive reagent N-acetylimidazole. Similarly, the arginine-reactive reagent glyoxal had only minor effects on the Na permeability. The results suggest that methionine is not critically involved in the kinetics of Na current inactivation. Similarly, an essential tyrosine or arginine residue seems to be unavailable to chemical reagents from outside on the frog node of Ranvier. Deduced from the reactivities of (some of) the reagents used, modification of membrane lipids is a tentative explanation for the effects observed on inactivation kinetics.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 2430631      PMCID: PMC1329833          DOI: 10.1016/S0006-3495(86)83495-6

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  30 in total

1.  Sodium channel inactivation in squid axon is removed by high internal pH or tyrosine-specific reagents.

Authors:  M S Brodwick; D C Eaton
Journal:  Science       Date:  1978-06-30       Impact factor: 47.728

2.  Effect of several "specific" chemical reagents on the Na+, K+ and leakage currents in voltage-clamped single nodes of Ranvier.

Authors:  J F Keana; R Stämpfli
Journal:  Biochim Biophys Acta       Date:  1974-11-27

3.  Arginine-specific reagents remove sodium channel inactivation.

Authors:  D C Eaton; M S Brodwick; G S Oxford; B Rudy
Journal:  Nature       Date:  1978-02-02       Impact factor: 49.962

4.  Effects of proteolytic enzymes on ionic conductances of squid axon membranes.

Authors:  C Sevcik; T Narahashi
Journal:  J Membr Biol       Date:  1975-12-04       Impact factor: 1.843

5.  Removal of sodium channel inactivation in squid giant axons by n-bromoacetamide.

Authors:  G S Oxford; C H Wu; T Narahashi
Journal:  J Gen Physiol       Date:  1978-03       Impact factor: 4.086

6.  Slow sodium inactivation in nerve after exposure to sulhydryl blocking reagents.

Authors:  P Shrager
Journal:  J Gen Physiol       Date:  1977-02       Impact factor: 4.086

7.  Destruction of the sodium conductance inactivation by a specific protease in perfused nerve fibres from Loligo.

Authors:  E Rojas; B Rudy
Journal:  J Physiol       Date:  1976-11       Impact factor: 5.182

8.  Effects of chemical modification of carboxyl groups on the voltage-clamped nerve fiber of the frog.

Authors:  M Rack; K H Woll
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

9.  Chemical modification of sodium channel surface charges in frog skeletal muscle by trinitrobenzene sulphonic acid.

Authors:  M D Cahalan; P A Pappone
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

10.  Interaction of deoxycholate with the sodium channel of squid axon membranes.

Authors:  C H Wu; P J Sides; T Narahashi
Journal:  J Gen Physiol       Date:  1980-09       Impact factor: 4.086

View more
  22 in total

1.  Na activation delays and their relation to inactivation in frog skeletal muscle.

Authors:  R Hahin
Journal:  J Membr Biol       Date:  1990-12       Impact factor: 1.843

2.  Mechanism of inactivation of single sodium channels after modification by chloramine-T, sea anemone toxin and scorpion toxin.

Authors:  K Nagy
Journal:  J Membr Biol       Date:  1988-11       Impact factor: 1.843

3.  Cytochemical localization of guanylate cyclase in photoreceptor cells of the mouse.

Authors:  U Schraermeyer; P Esser; S Grisanti; M Rack; K Heimann
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1997-03       Impact factor: 3.117

4.  Effects of chemical modification on Na channel function.

Authors:  M Rack; G Drews
Journal:  J Protein Chem       Date:  1989-06

5.  Voltage and temperature dependence of normal and chemically modified inactivation of sodium channels. Quantitative description by a cyclic three-state model.

Authors:  J Schmidtmayer
Journal:  Pflugers Arch       Date:  1989-07       Impact factor: 3.657

6.  Chloramine-T-induced modifications of K+ channel inactivation in neuroblastoma cells.

Authors:  B Rouzaire-Dubois; J M Dubois
Journal:  Pflugers Arch       Date:  1989       Impact factor: 3.657

7.  Na+ currents in cultured mouse pancreatic B-cells.

Authors:  T D Plant
Journal:  Pflugers Arch       Date:  1988-04       Impact factor: 3.657

8.  Removal of sodium inactivation and block of sodium channels by chloramine-T in crayfish and squid giant axons.

Authors:  J M Huang; J Tanguy; J Z Yeh
Journal:  Biophys J       Date:  1987-08       Impact factor: 4.033

9.  Mapping a region associated with Na channel inactivation using antibodies to a synthetic peptide corresponding to a part of the channel.

Authors:  H Meiri; G Spira; M Sammar; M Namir; A Schwartz; A Komoriya; E M Kosower; Y Palti
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

10.  The inactivating K+ current in GH3 pituitary cells and its modification by chemical reagents.

Authors:  G S Oxford; P K Wagoner
Journal:  J Physiol       Date:  1989-03       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.