Literature DB >> 224169

Dorsal root potentials and changes in extracellular potassium in the spinal cord of the frog.

R A Nicoll.   

Abstract

1. In the present study changes in extracellular potassium, ([K]e), were recorded in the isolated spinal cord of the frog with glial cell recordings and K-selective micro-electrodes to test the hypothesis that elevations in [K]e during neuronal activity produce the dorsal root potential (d.r.p.). 2. Sucrose gap recording from the dorsal root (d.r.) was used to record responses to root stimulation and to exogenously applied K+. 3. Stimulation of the ventral root, which elicits a d.r.p. in the frog spinal cord, was not associated with any change in [K]e, suggesting that d.r.p.s produced by ventral root stimulation are not due to changes in [K]e. 4. The largest change in [K]e observed following single stimuli to the dorsal root was 0.4 mM. Such a change in [K]e, if evenly distributed, would depolarize the dorsal root by about 1 mV and yet the simultaneously recorded d.r.p. evoked by stimulating an adjacent dorsal root (d.r.-d.r.p.) was over 10 mV. 5. The time-to-peak of the glidal cell responses was 10 times that of the d.r.-d.r.p. Low frequency (1-10 Hz) d.r. stimulation caused a decremental summation of glial cell responses, while there was no summation in the d.r.-d.r.p. These results suggest that the d.r.p. produced by single d.r. stimulation is generated in large part by a mechanism other than a change in [K]e. 6. During high frequency d.r. stimulation, which evoked 6-8 mM increases in [K]e, the adjacent d.r. was depolarized to a greater extent than that produced by single stimuli. The magnitude of this depolarization was similar to that produced by applying a [K]e equivalent to that observed in the spinal cord during high frequency stimulation. Thus, a substantial component of the sustained d.r. depolarization during high frequency d.r. stimulation may result from changes in [K]e. 7. In the presence of magnesium, high frequency d.r. stimulation evoked a picrotoxin resistant depolarization of an adjacent d.r. whose magnitude correlated well with the changes in [K]e recorded in the spinal cord. 8. In the presence of picrotoxin a slow, long duration depolarization of the d.r. occurred following single stimuli to the adjacent d.r. and the appearance and time course of this response correlated well with the time course of changes in [K]e. 9. Addition of K+ to the Ringer solution in concentrations up to 12 mM had a facilitatory action on reflex activity in the frog spinal cord. 10 The present results suggest that although changes in [K]e play a relatively minor role in generating d.r.p.s. elicited by single d.r. stimulation, the sustained dorsal root depolarization evoked either by high frequency stimulation or by single stimuli in the presence of picrotoxin may be due to a considerable extent to [K]e.

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Year:  1979        PMID: 224169      PMCID: PMC1278827          DOI: 10.1113/jphysiol.1979.sp012763

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


  36 in total

1.  Depolarization of primary afferents in the frog spinal cord under high Mg2+ concentrations.

Authors:  L Vyklický; E Syková; B Mellerová
Journal:  Brain Res       Date:  1976-11-19       Impact factor: 3.252

2.  Extracellular potassium and trasmitter release at the giant synapse of squid.

Authors:  S D Erulkar; F F Weight
Journal:  J Physiol       Date:  1977-04       Impact factor: 5.182

3.  A STUDY OF SPONTANEOUS MINIATURE POTENTIALS IN SPINAL MOTONEURONES.

Authors:  B KATZ; R MILEDI
Journal:  J Physiol       Date:  1963-09       Impact factor: 5.182

4.  Changes in potassium concentration around motor nerve terminals, produced by current flow, and their effects on neuromuscular transmission.

Authors:  A TAKEUCHI; N TAKEUCHI
Journal:  J Physiol       Date:  1961-01       Impact factor: 5.182

5.  The interpretation of potential changes in the spinal cord.

Authors:  D H Barron; B H Matthews
Journal:  J Physiol       Date:  1938-04-14       Impact factor: 5.182

6.  Potassium accumulation in muscle and associated changes.

Authors:  P J Boyle; E J Conway
Journal:  J Physiol       Date:  1941-08-11       Impact factor: 5.182

7.  The after effects of a tetanus on mammalian muscle.

Authors:  G L Brown; U S von Euler
Journal:  J Physiol       Date:  1938-06-14       Impact factor: 5.182

Review 8.  The role of GABA in primary afferent depolarization.

Authors:  R A Levy
Journal:  Prog Neurobiol       Date:  1977       Impact factor: 11.685

9.  Ultrastructural synaptology of Clarke's column.

Authors:  M Réthelyi
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

10.  Amino acids and presynaptic inhibition in the rat cuneate nucleus.

Authors:  N Davidson; C A Southwick
Journal:  J Physiol       Date:  1971-12       Impact factor: 5.182

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  14 in total

1.  Presynaptic NMDA receptors modulate glutamate release from primary sensory neurons in rat spinal cord dorsal horn.

Authors:  Rita Bardoni; Carole Torsney; Chi-Kun Tong; Massimiliano Prandini; Amy B MacDermott
Journal:  J Neurosci       Date:  2004-03-17       Impact factor: 6.167

2.  Accumulation of K+ in the synaptic cleft modulates activity by influencing both vestibular hair cell and calyx afferent in the turtle.

Authors:  Donatella Contini; Steven D Price; Jonathan J Art
Journal:  J Physiol       Date:  2016-11-04       Impact factor: 5.182

3.  Mechanisms involved in the depolarization of cutaneous afferents produced by segmental and descending inputs in the cat spinal cord.

Authors:  I Jiménez; P Rudomin; M Solodkin
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

4.  Extracellular potassium accumulation in the frog spinal cord induced by stimulation of the skin and ventrolateral columns.

Authors:  G Czéh; N Kríz; E Syková
Journal:  J Physiol       Date:  1981-11       Impact factor: 5.182

5.  Hyperpolarization of frog primary afferent fibres caused by activation of a sodium pump.

Authors:  R A Davidoff; J C Hackman
Journal:  J Physiol       Date:  1980-05       Impact factor: 5.182

6.  The signal-to-noise characteristics of rod-cone interaction.

Authors:  G M Bauer; T E Frumkes; R W Nygaard
Journal:  J Physiol       Date:  1983-04       Impact factor: 5.182

7.  Primary afferent activity, putative excitatory transmitters and extracellular potassium levels in frog spinal cord.

Authors:  R A Davidoff; J C Hackman; A M Holohean; J L Vega; D X Zhang
Journal:  J Physiol       Date:  1988-03       Impact factor: 5.182

8.  The supernormal period of the cerebellar parallel fibers effects of [Ca2+]o and [K+]o.

Authors:  R C Malenka; J D Kocsis; S G Waxman
Journal:  Pflugers Arch       Date:  1983-05       Impact factor: 3.657

9.  Primary afferent depolarization in the in vitro frog olfactory bulb.

Authors:  C E Jahr; R A Nicoll
Journal:  J Physiol       Date:  1981-09       Impact factor: 5.182

10.  Effects of extracellular potassium concentration on the excitability of the parallel fibres of the rat cerebellum.

Authors:  J D Kocsis; R C Malenka; S G Waxman
Journal:  J Physiol       Date:  1983-01       Impact factor: 5.182

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