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Potassium Fluxes in Dialyzed Squid Axons

Measurements have been made of K influx in squid giant axons under internal solute control by dialysis. With [ATP](i) = 1 µM, [Na](i) = 0, K influx was 6 ± 0.6 pmole/cm(2) sec; an increase to [ATP](i) = 4 mM gave an influx of 8 ± 0.5 pmole/cm(2) sec, while [ATP](i) 4, [Na](i) 80 gave a K influx of 1...

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Detalles Bibliográficos
Autores principales: Mullins, L. J., Brinley, F. J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1969
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2202880/
https://www.ncbi.nlm.nih.gov/pubmed/5795918
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author Mullins, L. J.
Brinley, F. J.
author_facet Mullins, L. J.
Brinley, F. J.
author_sort Mullins, L. J.
collection PubMed
description Measurements have been made of K influx in squid giant axons under internal solute control by dialysis. With [ATP](i) = 1 µM, [Na](i) = 0, K influx was 6 ± 0.6 pmole/cm(2) sec; an increase to [ATP](i) = 4 mM gave an influx of 8 ± 0.5 pmole/cm(2) sec, while [ATP](i) 4, [Na](i) 80 gave a K influx of 19 ± 0.7 pmole/cm(2) sec (all measurements at ∼16°C). Strophanthidin (10 µM) in seawater quantitatively abolished the ATP-dependent increase in K influx. The concentration dependence of ATP-dependent K influx on [ATP](i), [Na](i), and [K](o) was measured; an [ATP](i) of 30 µM gave a K influx about half that at physiological concentrations (2–3 mM). About 7 mM [Na](i) yielded half the K influx found at 80 mM [Na](i). The ATP-dependent K influx responded linearly to [K](o) from 1–20 mM and was independent of whether Na, Li, or choline was the principal cation of seawater. Substances tested as possible energy sources for the K pump were acetyl phosphate, phosphoarginine, PEP, and d-ATP. None was effective except d-ATP and this substance gave 70% of the maximal flux only when phosphoarginine or PEP was also present.
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spelling pubmed-22028802008-04-23 Potassium Fluxes in Dialyzed Squid Axons Mullins, L. J. Brinley, F. J. J Gen Physiol Article Measurements have been made of K influx in squid giant axons under internal solute control by dialysis. With [ATP](i) = 1 µM, [Na](i) = 0, K influx was 6 ± 0.6 pmole/cm(2) sec; an increase to [ATP](i) = 4 mM gave an influx of 8 ± 0.5 pmole/cm(2) sec, while [ATP](i) 4, [Na](i) 80 gave a K influx of 19 ± 0.7 pmole/cm(2) sec (all measurements at ∼16°C). Strophanthidin (10 µM) in seawater quantitatively abolished the ATP-dependent increase in K influx. The concentration dependence of ATP-dependent K influx on [ATP](i), [Na](i), and [K](o) was measured; an [ATP](i) of 30 µM gave a K influx about half that at physiological concentrations (2–3 mM). About 7 mM [Na](i) yielded half the K influx found at 80 mM [Na](i). The ATP-dependent K influx responded linearly to [K](o) from 1–20 mM and was independent of whether Na, Li, or choline was the principal cation of seawater. Substances tested as possible energy sources for the K pump were acetyl phosphate, phosphoarginine, PEP, and d-ATP. None was effective except d-ATP and this substance gave 70% of the maximal flux only when phosphoarginine or PEP was also present. The Rockefeller University Press 1969-06-01 /pmc/articles/PMC2202880/ /pubmed/5795918 Text en Copyright © 1969 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Mullins, L. J.
Brinley, F. J.
Potassium Fluxes in Dialyzed Squid Axons
title Potassium Fluxes in Dialyzed Squid Axons
title_full Potassium Fluxes in Dialyzed Squid Axons
title_fullStr Potassium Fluxes in Dialyzed Squid Axons
title_full_unstemmed Potassium Fluxes in Dialyzed Squid Axons
title_short Potassium Fluxes in Dialyzed Squid Axons
title_sort potassium fluxes in dialyzed squid axons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2202880/
https://www.ncbi.nlm.nih.gov/pubmed/5795918
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