Literature DB >> 690884

Amino acid pharmacology of mammalian central neurones grown in tissue culture.

J L Barker, B R Ransom.   

Abstract

1. Spinal and cerebellar-brainstem areas of fetal mouse were dissociated and grown in tissue culture until large enough to permit stable intracellular recording. 2. The tissue-cultured neurones, growing as a monolayer and accessible under direct vision using phase contrast optics, allowed precise placement of intracellular recording and extracellular ionophoretic pipettes. 3. Ionophoresis of GABA and glutamate revealed a non-uniform distribution of responses over the cell surface, with a lack of spatial coincidence in sensitivity between the two. GABA inhibited and glutamate excited all cells tested. 4. GABA responses evoked at the cell body and on nearby process membrane were almost uniformly hyperpolarizing, while those at some peripheral process membrane were either hyperpolarizing, depolarizing or a combination of both events. All responses were associated with an increase in membrane slope conductance. 5. Membrane polarization showed that all hyperpolarizing events extrapolated to about the same inversion potential, which averaged about 9 mV more negative than resting potential (n = 95 cells). The depolarizing phases of responses evoked at peripheral membranes extrapolated to about 0 mV (n = 5 cells). 6. The hyperpolarization and increase in membrane conductance of GABA responses at the cell body were dependent on Cl- ions and the inversion potential of the response was dependent on the Cl- ion concentration gradient. The inversion potentials of GABA, glycine and beta-alanine responses were identical. 7. When matched in magnitude for evoked conductance increase, glycine responses decayed more rapidly than GABA. Glycine and beta-alanine voltage responses both decayed faster than GABA responses of comparable size. 8. In about half the cells tested sustained or rapidly repeated application of GABA and glycine transformed hyperpolarizing responses into depolarizations which were associated with a maintained conductance increase. Results from conditioning-test experiments with pairs of GABA and glycine responses suggest that the reversal of response polarity is due to a rapid redistribution of Cl- ions. 9. The limiting slope of log-log dose-response curves for GABA-induced conductance averaged about 2, while those for glutamate-induced depolarizations averaged about 1. The results suggest that two molecules of GABA and one molecule of glutamate participate in the respective post-synaptic responses. 10. The observation indicate that mammalian C.N.S. tissue grown in culture is a suitable model to study C.N.S. membrane pharmacology with increasing precision.

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Year:  1978        PMID: 690884      PMCID: PMC1282662          DOI: 10.1113/jphysiol.1978.sp012387

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


  49 in total

1.  Iontophoretic studies of neurones in the mammalian cerebral cortex.

Authors:  K KRNJEVIC; J W PHILLIS
Journal:  J Physiol       Date:  1963-02       Impact factor: 5.182

2.  The influence of potassium and chloride ions on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

3.  Physiological and kinetic properties of cholinergic receptors activated by multiaction interneurons in buccal ganglia of Aplysia.

Authors:  D Gardner; E R Kandel
Journal:  J Neurophysiol       Date:  1977-03       Impact factor: 2.714

4.  GABA and glycine actions on spinal motoneurons.

Authors:  K Krnjević; E Puil; R Werman
Journal:  Can J Physiol Pharmacol       Date:  1977-06       Impact factor: 2.273

5.  Mouse spinal cord in cell culture. III. Neuronal chemosensitivity and its relationship to synaptic activity.

Authors:  B R Ransom; P N Bullock; P G Nelson
Journal:  J Neurophysiol       Date:  1977-09       Impact factor: 2.714

6.  Differential chemosensitivity of synaptic and extrasynaptic areas on the neuronal surface membrane in parasympathetic neurons of the frog, tested by microapplication of acetylcholine.

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

7.  Pentobarbitone pharmacology of mammalian central neurones grown in tissue culture.

Authors:  J L Barker; B R Ransom
Journal:  J Physiol       Date:  1978-07       Impact factor: 5.182

8.  Mouse spinal cord in cell culture. II. Synaptic activity and circuit behavior.

Authors:  B R Ransom; C N Christian; P N Bullock; P G Nelson
Journal:  J Neurophysiol       Date:  1977-09       Impact factor: 2.714

9.  Mouse spinal cord in cell culture. I. Morphology and intrinsic neuronal electrophysiologic properties.

Authors:  B R Ransom; E Neale; M Henkart; P N Bullock; P G Nelson
Journal:  J Neurophysiol       Date:  1977-09       Impact factor: 2.714

10.  Acetylcholine receptors: topographic distribution and pharmacological properties of two receptor types on a single molluscan neurone.

Authors:  H Levitan; L Tauc
Journal:  J Physiol       Date:  1972-05       Impact factor: 5.182

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  41 in total

1.  Modulation of mammalian dendritic GABA(A) receptor function by the kinetics of Cl- and HCO3- transport.

Authors:  K J Staley; W R Proctor
Journal:  J Physiol       Date:  1999-09-15       Impact factor: 5.182

2.  GABA-evoked chloride currents do not differ between dendrites and somata of rat neocortical neurons.

Authors:  J F van Brederode; T Takigawa; C Alzheimer
Journal:  J Physiol       Date:  2001-06-15       Impact factor: 5.182

3.  Expression of the voltage-gated chloride channel ClC-2 in rod bipolar cells of the rat retina.

Authors:  R Enz; B J Ross; G R Cutting
Journal:  J Neurosci       Date:  1999-11-15       Impact factor: 6.167

4.  Kinetic properties of the glycine receptor main- and sub-conductance states of mouse spinal cord neurones in culture.

Authors:  R E Twyman; R L Macdonald
Journal:  J Physiol       Date:  1991-04       Impact factor: 5.182

5.  gamma-Aminobutyric acid responses in rat locus coeruleus neurones in vitro: a current-clamp and voltage-clamp study.

Authors:  S S Osmanović; S A Shefner
Journal:  J Physiol       Date:  1990-02       Impact factor: 5.182

6.  Imaging synaptic inhibition in transgenic mice expressing the chloride indicator, Clomeleon.

Authors:  Ken Berglund; Wolfram Schleich; Patrik Krieger; Li Shen Loo; Dongqing Wang; Nell B Cant; Guoping Feng; George J Augustine; Thomas Kuner
Journal:  Brain Cell Biol       Date:  2008-04-05

7.  Glycine induces two distinct membrane currents in neonatal rat sympathetic preganglionic neurones in vitro.

Authors:  S Y Wu; T Miyazaki; N J Dun
Journal:  J Physiol       Date:  1995-03-01       Impact factor: 5.182

8.  Convulsant-induced depression of amino acid responses in cultured mouse spinal neurones studied under voltage clamp.

Authors:  J L Barker; R N McBurney; D A Mathers
Journal:  Br J Pharmacol       Date:  1983-12       Impact factor: 8.739

9.  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

10.  Two different responses of hippocampal pyramidal cells to application of gamma-amino butyric acid.

Authors:  P Andersen; R Dingledine; L Gjerstad; I A Langmoen; A M Laursen
Journal:  J Physiol       Date:  1980-08       Impact factor: 5.182

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