Literature DB >> 1255512

The ionic basis of the resting potential and a slow depolarizing response in Rohon-Beard neurones of Xenopus tadpoles.

N C Spitzer.   

Abstract

1. Rohon-Beard cells in the spinal cord of Xenopus laevis tadpoles have been studied in animals 4-days to 2-weeks-old (Nieuwkoop & Faber, 1956, stages 45-49). These neurones have an unusually large resting membrane potential of -88 mV, in Ringer solution containing 3-0 mM K+. 2. Their resting potential (R..) depends on the concentration gradient of K+ across the cell membrane. These cells follow the prediction of the Nernst equation for a K+-selective electrode, down to external K+ concentrations as low as 1-0 mM (R.P. -118 mV). 3. The resting potentials of muscle cells in these animals exhibit the same dependence on external [K+], as has been shown previously. 4. Rohon-Beard cells can be driven antidromically, bu stimulation of the anterior end of the spinal cord with brief current pulses through a suction electrode. Antidromic action potentials fail to invade the cell body with repeated stimulation at 1Hz. 5. Even when impulses fail to invade Rohon-Beard somata, slow depolarizations can be produced by single shocks or trains of shocks which cause impulse activity in other neurones. The response can be observed to a single stimulus or to a train of stimuli. The magnitude of the depolarization is graded, depending on the number of stimuli and the frequency of stimulation. 6. Support is presented for the hypothesis that the slow depolarization in Rohon-Beard cells is mediated by the release of K+ into their environment by the impulse activity of neighbouring neurones. The slow depolarization increases in solutions containing 1-5 mM-K+, and decreases in solutions containing 6-0 mM-K+. The changes are in quantitative agreement with those anticipated by theory. 7. The slow depolarization is unlikely to be due to a conductance change produced by a synaptic transmitter, since hyperpolarization and depolarization of the Rohon-Beard cell with injected current do not change the amplitude of the response. Further, low Ca-high Mg solutions which block neuromuscular transmission do not block the response. 8. The possible role of the slow depolarizing response in the physiological activity of these neurones is discussed.

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Year:  1976        PMID: 1255512      PMCID: PMC1309237          DOI: 10.1113/jphysiol.1976.sp011272

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


  27 in total

1.  Visual identification of synaptic boutons on living ganglion cells and of varicosities in postganglionic axons in the heart of the frog.

Authors:  U J McMahan; S W Kuffler
Journal:  Proc R Soc Lond B Biol Sci       Date:  1971-04-27

2.  Synaptic transmission and its duplication by focally applied acetylcholine in parasympathetic neurons in the heart of the frog.

Authors:  M J Dennis; A J Harris; S W Kuffler
Journal:  Proc R Soc Lond B Biol Sci       Date:  1971-04-27

3.  Electrophysiologic and morphologic properties of neurons in dissociated chick spinal cord cell cultures.

Authors:  G D Fischbach; M A Dichter
Journal:  Dev Biol       Date:  1974-03       Impact factor: 3.582

4.  Intracellular and intercellular potentials in the early amphibian embryo.

Authors:  C Slack; A E Warner
Journal:  J Physiol       Date:  1973-07       Impact factor: 5.182

5.  Excitability and conduction in neurons of dissociated ganglionic cell cultures.

Authors:  S Varon; C Raiborn
Journal:  Brain Res       Date:  1971-07-09       Impact factor: 3.252

6.  Extracellular K + activity and slow potential changes in spinal cord and medulla.

Authors:  K Krnjević; M E Morris
Journal:  Can J Physiol Pharmacol       Date:  1972-12       Impact factor: 2.273

7.  Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leech.

Authors:  D A Baylor; J G Nicholls
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

8.  After-effects of nerve impulses on signalling in the central nervous system of the leech.

Authors:  D A Baylor; J G Nicholls
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

9.  Evidence for cholinergic synapses between dissociated rat sympathetic neurons in cell culture.

Authors:  P H O'Lague; K Obata; P Claude; E J Furshpan; D D Potter
Journal:  Proc Natl Acad Sci U S A       Date:  1974-09       Impact factor: 11.205

10.  New membrane formation during cytokinesis in normal and cytochalasin B-treated eggs of Xenopus laevis. II. Electrophysiological observations.

Authors:  W S de Laat; J G Bluemink
Journal:  J Cell Biol       Date:  1974-03       Impact factor: 10.539

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  18 in total

1.  The development of the action potential mechanism of amphibian neurons isolated in culture.

Authors:  N C Spitzer; J E Lamborghini
Journal:  Proc Natl Acad Sci U S A       Date:  1976-05       Impact factor: 11.205

2.  Dorsal-ventral gradient for neuronal plasticity in the embryonic spinal cord.

Authors:  Ricardo H Pineda; Angeles B Ribera
Journal:  J Neurosci       Date:  2008-04-02       Impact factor: 6.167

3.  Zebrafish In Situ Spinal Cord Preparation for Electrophysiological Recordings from Spinal Sensory and Motor Neurons.

Authors:  Rosa L Moreno; Megan Josey; Angeles B Ribera
Journal:  J Vis Exp       Date:  2017-04-18       Impact factor: 1.355

4.  Voltage-gated calcium currents in cultured embryonic Xenopus spinal neurones.

Authors:  M E Barish
Journal:  J Physiol       Date:  1991-12       Impact factor: 5.182

5.  Action potentials of embryonic dorsal root ganglion neurones in Xenopus tadpoles.

Authors:  P I Baccaglini
Journal:  J Physiol       Date:  1978-10       Impact factor: 5.182

6.  Contractile activation in myotomes from developing larvae of Xenopus laevis.

Authors:  C L Huang
Journal:  J Physiol       Date:  1986-06       Impact factor: 5.182

7.  Excitatory amino acid receptors in Xenopus embryo spinal cord and their role in the activation of swimming.

Authors:  N Dale; A Roberts
Journal:  J Physiol       Date:  1984-03       Impact factor: 5.182

8.  The appearance and development of chemosensitivity in Rohon-Beard neurones of the Xenopus spinal cord.

Authors:  J L Bixby; N C Spitzer
Journal:  J Physiol       Date:  1982-09       Impact factor: 5.182

9.  Formation of electrical coupling between embryonic Xenopus muscle cells in culture.

Authors:  I Chow; M M Poo
Journal:  J Physiol       Date:  1984-01       Impact factor: 5.182

10.  Zebrafish touch-insensitive mutants reveal an essential role for the developmental regulation of sodium current.

Authors:  A B Ribera; C Nüsslein-Volhard
Journal:  J Neurosci       Date:  1998-11-15       Impact factor: 6.167

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