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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.
Adams,
Actions of gamma-aminobutyric acid on sympathetic ganglion cells.
1975, Pubmed
Adams,
Actions of gamma-aminobutyric acid on sympathetic ganglion cells.
1975,
Pubmed
Adams,
A study of desensitization using voltage clamp.
1975,
Pubmed
Andersen,
Two different responses of hippocampal pyramidal cells to application of gamma-amino butyric acid.
1980,
Pubmed
Baccaglini,
Developmental changes in the inward current of the action potential of Rohon-Beard neurones.
1977,
Pubmed
,
Xenbase
Barker,
Amino acid pharmacology of mammalian central neurones grown in tissue culture.
1978,
Pubmed
Barker,
The pharmacology and ionic dependency of amino acid responses in the frog spinal cord.
1973,
Pubmed
Bennett,
Gap junctions, electrotonic coupling, and intercellular communication.
1978,
Pubmed
,
Xenbase
Bevan,
The distribution of alpha-bungarotoxin binding sites of mammalian skeletal muscle developing in vivo.
1977,
Pubmed
Blackshaw,
Low resistance junctions between mesoderm cells during development of trunk muscles.
1976,
Pubmed
,
Xenbase
Blackshaw,
Onset of acetylcholine sensitivity and endplate activity in developing myotome muscles of Xenopus.
1976,
Pubmed
,
Xenbase
Brookes,
Discrete states of responsiveness of a locust muscle gamma-aminobutyric acid receptor: the influence of extracellular ion concentrations.
1980,
Pubmed
Burden,
Development of the neuromuscular junction in the chick embryo: the number, distribution, and stability of acetylcholine receptors.
1977,
Pubmed
Choi,
GABA conductance of chick spinal cord and dorsal root ganglion neurons in cell culture.
1981,
Pubmed
Colquhoun,
The actions of tubocurarine at the frog neuromuscular junction.
1979,
Pubmed
Dennis,
Development of neuromuscular junctions in rat embryos.
1981,
Pubmed
Diamond,
Analysis of Mauthner cell responses to iontophoretically delivered pulses of GABA, glycine and L-glutamate.
1973,
Pubmed
DIAMOND,
A study of foetal and new-born rat muscle fibres.
1962,
Pubmed
Dichter,
Physiological identification of GABA as the inhibitory transmitter for mammalian cortical neurons in cell culture.
1980,
Pubmed
Dunlap,
Neurotransmitters decrease the calcium ocmponent of sensory neurone action potentials.
,
Pubmed
Gallagher,
Characterization and ionic basis of GABA-induced depolarizations recorded in vitro from cat primary afferent neurones.
1978,
Pubmed
Goodman,
Embryonic development of identified neurones: differentiation from neuroblast to neurone.
1979,
Pubmed
Goodman,
The development of electrical properties of identified neurones in grasshopper embryos.
1981,
Pubmed
Goodman,
Embryonic development of identified neurons: origin and transformation of the H cell.
1981,
Pubmed
Harris,
Differential chemosensitivity of synaptic and extrasynaptic areas on the neuronal surface membrane in parasympathetic neurons of the frog, tested by microapplication of acetylcholine.
1971,
Pubmed
Horn,
Alpha-drenergic inhibition of calcium-dependent potentials in rat sympathetic neurones.
1980,
Pubmed
KATZ,
On the factors which determine the amplitude of the miniature end-plate potential.
1957,
Pubmed
Krnjević,
GABA and glycine actions on spinal motoneurons.
1977,
Pubmed
Lamborghini,
Rohon-beard cells and other large neurons in Xenopus embryos originate during gastrulation.
1980,
Pubmed
,
Xenbase
Nishi,
Primary afferent neurones: the ionic mechanism of GABA-mediated depolarization.
1974,
Pubmed
Ohmori,
Development of neuromuscular transmission in a larval tunicate.
1977,
Pubmed
Potter,
Connections between cells of the developing squid as revealed by electrophysiological methods.
1966,
Pubmed
Ravdin,
Inhibition of neuronal acetylcholine sensitivity by alpha-toxins from Bungarus multicinctus venom.
1979,
Pubmed
Ritchie,
Electrophysiological properties of the membrane and acetylcholine receptor in developing rat and chick myotubes.
1975,
Pubmed
Spitzer,
Voltage- and stage-dependent uncoupling of Rohon-Beard neurones during embryonic development of Xenopus tadpoles.
1982,
Pubmed
,
Xenbase
Spitzer,
The ionic basis of the resting potential and a slow depolarizing response in Rohon-Beard neurones of Xenopus tadpoles.
1976,
Pubmed
,
Xenbase
TAKEUCHI,
LOCALIZED ACTION OF GAMMA-AMINOBUTYRIC ACID ON THE CRAYFISH MUSCLE.
1965,
Pubmed
TAKEUCHI,
On the permeability of end-plate membrane during the action of transmitter.
1960,
Pubmed
THESLEFT,
The mode of neuromuscular block caused by acetylcholine, nicotine, decamethonium and succinylcholine.
1955,
Pubmed
Yarowsky,
Receptors for gamma-aminobutyric acid (GABA) on Aplysia neurons.
1978,
Pubmed
Ziskind,
Depolarising effect of curare on embryonic rat muscles.
1978,
Pubmed