Literature DB >> 132526

Post-tetanic hyperpolarization, sodium-potassium-activated adenosine triphosphatase and high energy phosphate levels in garfish olfactory nerve.

D B McDougal, L A Osborn.   

Abstract

1. While much is now known about the Na-K-ATPase and the posttetanic hyperpolarization of nervous tissue, they have yet to be studied together in the same preparation. 2. The post-tetanic hyperpolarization was studied in desheathed garfish olfactory nerve. The rate constant of decay of the post-tetanic hyperpolarization was determined by monitoring difference potentials after stimulation at 1/sec for 2-3 min. 3. In membrane fractions prepared from these nerves, the ouabain-sensitive ATPase activity (Na-K-ATPase) was determined by spectrophotometric measurements. 4. Both the post-tetanic hyperpolarization and the Na-K-ATPase showed a similar sigmoidal dependence on K+ concentration. The sequence of cation specificities measured at the K-site of the enzyme was the same as that determined by post-tetanic hyperpolarization measurements in whole nerve. 5. The rate constants of the enzyme showed a dependence on Na+ concentration that paralleled the way in which the post-tetanic hyperpolarization rate constants varied as a function of the number of impulses. When Na+ was completely replaced by Li+, neither enzyme activity nor post-tetanic hyperpolarization could be measured. 6. The pH optimum for enzyme activity was between pH 7-0 and 7-8, while the optimal pH for post-tetanic hyperpolarization was above pH 8-0. 7. Metabolite levels in preparations of this nerve studied in vitro correspond to levels found in vivo. 8. High energy phosphate levels were measured fluorometrically in extracts of nerve samples that had been stimulated in air at 1/sec for various intervals. 9. During the first 2 min of stimulation, there was a significant accumulation of inorganic phosphate, and the ATP/ADP.Pi ratio dropped appreciably. 10. The accumulation of ATPase products was commensurate with the approach of post-tetanic hyperpolarization rate constants to their maximum level. This provides direct evidence for an ATPase functioning in active Na+ transport in nerve. 11. The garfish Na-K-ATPase is sensitive to the ATP/ADP ratio of the incubating medium, but is relatively insensitive to orthophosphate, Pi. The fall in post-tetanic hyperpolarization rate constants observed with continued nerve stimulation may have been partially due to the falling ATP/ADP ratio measured in nerve under similar conditions.

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Year:  1976        PMID: 132526      PMCID: PMC1309290          DOI: 10.1113/jphysiol.1976.sp011310

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


  29 in total

1.  The movement of potassium ions during electrical activity, and the kinetics of the recovery process, in the non-myelinated fibres of the garfish olfactory nerve.

Authors:  J M Ritchie; R W Straub
Journal:  J Physiol       Date:  1975-07       Impact factor: 5.182

2.  Studies on the interaction of ouabain and other cardio-active steroids with sodium-potassium-activated adenosine triphosphatase.

Authors:  R W Albers; G J Koval
Journal:  Mol Pharmacol       Date:  1968-07       Impact factor: 4.436

3.  Phosphorus metabolism of intact crab nerve and its relation to the active transport of ions.

Authors:  P F Baker
Journal:  J Physiol       Date:  1965-09       Impact factor: 5.182

4.  Kinetic studies on a brain microsomal adenosine triphosphatase. Evidence suggesting conformational changes.

Authors:  J D Robinson
Journal:  Biochemistry       Date:  1967-10       Impact factor: 3.162

5.  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

6.  An axon plasma membrane preparation from the walking legs of the lobster Homarus americanus.

Authors:  J L Denburg
Journal:  Biochim Biophys Acta       Date:  1972-09-01

7.  Kinetic studies of membrane (Na+-K+-Mg2+)-ATPase.

Authors:  T Hexum; F E Samson; R H Himes
Journal:  Biochim Biophys Acta       Date:  1970-08-15

8.  Intracellular sodium activity and the sodium pump in snail neurones.

Authors:  R C Thomas
Journal:  J Physiol       Date:  1972-01       Impact factor: 5.182

9.  Physiological and biochemical changes in frog sciatic nerve during anoxia and recovery.

Authors:  Y Okada; D B McDougal
Journal:  J Neurochem       Date:  1971-12       Impact factor: 5.372

10.  Impulses at the artifactual nerve end.

Authors:  D M Easton
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1965
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  6 in total

Review 1.  Molecular mechanisms of memory formation.

Authors:  K T Ng; M E Gibbs; S F Crowe; G L Sedman; F Hua; W Zhao; B O'Dowd; N Rickard; C L Gibbs; E Syková
Journal:  Mol Neurobiol       Date:  1991       Impact factor: 5.590

2.  Increase in efflux of inorganic phosphate during electrical activity in small non-myelinated nerve fibres.

Authors:  J M Ritchie; R W Straub
Journal:  J Physiol       Date:  1978-01       Impact factor: 5.182

3.  Phosphate efflux and oxygen consumption in small non-myelinated nerve fibres at rest and during activity.

Authors:  J M Ritchie; R W Straub
Journal:  J Physiol       Date:  1979-02       Impact factor: 5.182

4.  Effects of divalent cations on responses of a sympathetic ganglion to 5-hydroxytryptamine and 1,1-dimethyl-4-phenyl piperazinium.

Authors:  H L Nash; D I Wallis
Journal:  Br J Pharmacol       Date:  1981-07       Impact factor: 8.739

5.  The electrogenic potential in rat C nerve fibres: some effects of lithium and thallium.

Authors:  I C Smith
Journal:  J Physiol       Date:  1979-09       Impact factor: 5.182

Review 6.  Ion dynamics during seizures.

Authors:  Joseph V Raimondo; Richard J Burman; Arieh A Katz; Colin J Akerman
Journal:  Front Cell Neurosci       Date:  2015-10-21       Impact factor: 5.505

  6 in total

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