Literature DB >> 6294289

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

J L Bixby, N C Spitzer.   

Abstract

1. We have examined the onset and subsequent development of chemosensitivity in Rohon-Beard neurones from the Xenopus spinal cord. These cells become sensitive to bath-applied gamma-aminobutyric acid (GABA) around stage 25 (early tailbud, about 1 d old), and remain so at least until stage 49 (9 d old). In contrast, a number of other neurotransmitter candidates tested caused no potential or conductance change during the same period.2. We examined ionophoretic dose-response relations of the cells at stage 26, a couple of hours after the first acquisition of GABA sensitivity. Sensitivities as high as 450 mV/nC were recorded. Comparable sensitivities were recorded between stages 46-49 (5-9 d old).3. Measurements of ionophoretic sensitivities and input resistances during several periods from stage 26 to maturity show that the underlying conductance change for a given GABA dose is likely to increase steadily during this time. A ;sensitivity index' (ionophoretic sensitivity/input resistance) was calculated, which is low at stage 26, higher at intermediate stages (stages 31-42), and highest for mature cells (stages 46-49; 5-9 d of development).4. The reversal potential of the ionophoretic GABA response is the same at stage 26 (-30 mV) as it is in mature cells. Ion substitution experiments show that Na(+) and K(+), but not Cl(-) or Ca(2+), are involved in the response.5. GABA responses at stage 26 are pharmacologically similar to those of mature cells. The responses are blocked by 10 muM-picrotoxin or curare, and muscimol is an agonist in concentrations as low as 1 muM.6. GABA responses at stage 26 desensitize in a manner similar to that seen for mature cells, either with prolonged bath application of GABA or with repetitive ionophoretic application.7. Nearly half of the cells tested at stage 26 respond to glycine, in concentrations as low as 5 muM. This sensitivity is absent by 3(1/2) d of development.8. The responses of Rohon-Beard neurones to GABA are similar to those of other cells in that they involve a conductance increase, are mimicked by muscimol, and are blocked by picrotoxin. These responses are different in that they do not involve Cl(-) and are blocked by low concentrations of curare.9. Many of the characteristics of GABA receptors, i.e. the reversal potential, desensitization, and pharmacology, are constant during development. However, the sensitivity of the cells to GABA and the spectrum of transmitters to which they are sensitive appear to change.

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Year:  1982        PMID: 6294289      PMCID: PMC1225313          DOI: 10.1113/jphysiol.1982.sp014356

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


  40 in total

1.  LOCALIZED ACTION OF GAMMA-AMINOBUTYRIC ACID ON THE CRAYFISH MUSCLE.

Authors:  A TAKEUCHI; N TAKEUCHI
Journal:  J Physiol       Date:  1965-03       Impact factor: 5.182

2.  Embryonic development of identified neurons: origin and transformation of the H cell.

Authors:  C S Goodman; M Bate; N C Spitzer
Journal:  J Neurosci       Date:  1981-01       Impact factor: 6.167

3.  Depolarising effect of curare on embryonic rat muscles.

Authors:  L Ziskind; M J Dennis
Journal:  Nature       Date:  1978-12-07       Impact factor: 49.962

4.  Development of neuromuscular junctions in rat embryos.

Authors:  M J Dennis; L Ziskind-Conhaim; A J Harris
Journal:  Dev Biol       Date:  1981-01-30       Impact factor: 3.582

5.  Low resistance junctions between mesoderm cells during development of trunk muscles.

Authors:  S E Blackshaw; A E Warner
Journal:  J Physiol       Date:  1976-02       Impact factor: 5.182

6.  The pharmacology and ionic dependency of amino acid responses in the frog spinal cord.

Authors:  J L Barker; R A Nicoll
Journal:  J Physiol       Date:  1973-01       Impact factor: 5.182

7.  The development of electrical properties of identified neurones in grasshopper embryos.

Authors:  C S Goodman; N C Spitzer
Journal:  J Physiol       Date:  1981       Impact factor: 5.182

8.  Analysis of Mauthner cell responses to iontophoretically delivered pulses of GABA, glycine and L-glutamate.

Authors:  J Diamond; S Roper
Journal:  J Physiol       Date:  1973-07       Impact factor: 5.182

9.  Rohon-beard cells and other large neurons in Xenopus embryos originate during gastrulation.

Authors:  J E Lamborghini
Journal:  J Comp Neurol       Date:  1980-01-15       Impact factor: 3.215

10.  Characterization and ionic basis of GABA-induced depolarizations recorded in vitro from cat primary afferent neurones.

Authors:  J P Gallagher; H Higashi; S Nishi
Journal:  J Physiol       Date:  1978-02       Impact factor: 5.182

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  12 in total

1.  Evidence that different cation chloride cotransporters in retinal neurons allow opposite responses to GABA.

Authors:  N Vardi; L L Zhang; J A Payne; P Sterling
Journal:  J Neurosci       Date:  2000-10-15       Impact factor: 6.167

2.  Differentiation of voltage-gated potassium current and modulation of excitability in cultured amphibian spinal neurones.

Authors:  M E Barish
Journal:  J Physiol       Date:  1986-06       Impact factor: 5.182

3.  Embryonically expressed GABA and glutamate drive electrical activity regulating neurotransmitter specification.

Authors:  Cory M Root; Norma A Velázquez-Ulloa; Gabriela C Monsalve; Elena Minakova; Nicholas C Spitzer
Journal:  J Neurosci       Date:  2008-04-30       Impact factor: 6.167

4.  Increases in intracellular calcium ion concentration during depolarization of cultured embryonic Xenopus spinal neurones.

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

5.  On the basis of delayed depolarization and its role in repetitive firing of Rohon-Beard neurones in Xenopus tadpoles.

Authors:  N C Spitzer
Journal:  J Physiol       Date:  1984-12       Impact factor: 5.182

6.  Sensory physiology, anatomy and immunohistochemistry of Rohon-Beard neurones in embryos of Xenopus laevis.

Authors:  J D Clarke; B P Hayes; S P Hunt; A Roberts
Journal:  J Physiol       Date:  1984-03       Impact factor: 5.182

7.  Nicotinic and muscarinic ACh receptors in rhythmically active spinal neurones in the Xenopus laevis embryo.

Authors:  R Perrins; A Roberts
Journal:  J Physiol       Date:  1994-07-15       Impact factor: 5.182

8.  Ionic and pharmacological properties of reciprocal inhibition in Xenopus embryo motoneurones.

Authors:  S R Soffe
Journal:  J Physiol       Date:  1987-01       Impact factor: 5.182

9.  GABAB receptors modulate glycinergic inhibition and spike threshold in Xenopus embryo spinal neurones.

Authors:  M J Wall; N Dale
Journal:  J Physiol       Date:  1993-09       Impact factor: 5.182

10.  The appearance and development of neurotransmitter sensitivity in Xenopus embryonic spinal neurones in vitro.

Authors:  J L Bixby; N C Spitzer
Journal:  J Physiol       Date:  1984-08       Impact factor: 5.182

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