Literature DB >> 8308724

Characteristics of multiple voltage-activated K+ currents in acutely dissociated chick ciliary ganglion neurones.

M E Wisgirda1, S E Dryer.   

Abstract

1. The properties of voltage-activated K+ currents were examined using whole-cell recording techniques in acutely isolated chick ciliary ganglion neurones. 2. Application of depolarizing voltage pulses from a holding potential of -60 mV evoked sustained outward currents that inactivated with time constants of hundreds of milliseconds (IDR). Bath application of 10 mM tetraethylammonium (TEA) caused a 70-90% reduction of IDR. Application of depolarizing voltage steps from a holding potential of -120 mV revealed a second class of TEA-resistant outward currents. These currents activated quickly but inactivated completely within tens of milliseconds (IA). IA activated at more negative command potentials than IDR. However, IDR exhibited a steeper voltage dependence of activation than IA. 3. The midpoint of the steady-state inactivation curve of IA was between -95 and -110 mV. By contrast the midpoint of the steady-state inactivation curve of IDR was between -80 and -90 mV. It was not possible to produce a complete inactivation of IDR using prepulses of up to 2 s duration. 4. The time course of IA inactivation could only be fitted with double-exponential curves with time constants of 5-18 ms and 30-60 ms at membrane potentials positive to -30 mV. The inactivation of IA was slower at more positive membrane potentials because of a greater contribution of the long time constant. The individual time constants were not markedly voltage dependent. 5. Bath application of 5 mM 4-aminopyridine (4-AP) caused a 70-100% block of IA whereas 1 mM 4-AP was ineffective. Bath application of 560 nM alpha-dendrotoxin (DTX) produced a 50-70% reduction of IA, but application of 280 nM DTX had no effect on IA. 6. Application of 1 mM 4-AP produced a reversible 55-80% block of IDR measured at the end of a 500 ms depolarizing pulse. The 4-AP-sensitive components of IDR activated rapidly and exhibited a gradual inactivation with continued depolarization. The 4-AP-resistant components of IDR activated much more slowly and showed very little tendency to inactivate. Significant blockade of IDR was produced by 10 microM 4-AP. 7. The decay of IDR tail currents could only be fitted with double exponential curves with time constants of 3-6 and 40-60 ms, respectively. The fast and slow components of the tail currents behaved independently with respect to the duration of the depolarizing voltage step. 8. Application of 1 mM 4-AP eliminated the fast, but not the slow component of IDR tail currents.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8308724      PMCID: PMC1143912          DOI: 10.1113/jphysiol.1993.sp019853

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


  31 in total

1.  An inward rectifier is present in presynaptic nerve terminals in the chick ciliary ganglion.

Authors:  G H Fletcher; V A Chiappinelli
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2.  Alternative splicing contributes to K+ channel diversity in the mammalian central nervous system.

Authors:  C J Luneau; J B Williams; J Marshall; E S Levitan; C Oliva; J S Smith; J Antanavage; K Folander; R B Stein; R Swanson
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

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Authors:  A L HODGKIN; A F HUXLEY
Journal:  J Physiol       Date:  1952-04       Impact factor: 5.182

4.  Heteromultimeric channels formed by rat brain potassium-channel proteins.

Authors:  J P Ruppersberg; K H Schröter; B Sakmann; M Stocker; S Sewing; O Pongs
Journal:  Nature       Date:  1990-06-07       Impact factor: 49.962

5.  K+ current diversity is produced by an extended gene family conserved in Drosophila and mouse.

Authors:  A Wei; M Covarrubias; A Butler; K Baker; M Pak; L Salkoff
Journal:  Science       Date:  1990-05-04       Impact factor: 47.728

6.  4-Aminopyridine and dendrotoxin induce repetitive firing in rat visceral sensory neurones by blocking a slowly inactivating outward current.

Authors:  C E Stansfeld; S J Marsh; J V Halliwell; D A Brown
Journal:  Neurosci Lett       Date:  1986-03-14       Impact factor: 3.046

7.  Heteropolymeric potassium channels expressed in Xenopus oocytes from cloned subunits.

Authors:  M J Christie; R A North; P B Osborne; J Douglass; J P Adelman
Journal:  Neuron       Date:  1990-03       Impact factor: 17.173

8.  Changes in densities and kinetics of delayed rectifier potassium channels during neuronal differentiation.

Authors:  G L Harris; L P Henderson; N C Spitzer
Journal:  Neuron       Date:  1988-10       Impact factor: 17.173

Review 9.  Tetraethylammonium ions and the potassium permeability of excitable cells.

Authors:  P R Stanfield
Journal:  Rev Physiol Biochem Pharmacol       Date:  1983       Impact factor: 5.545

10.  Three pharmacologically distinct potassium channels in molluscan neurones.

Authors:  S H Thompson
Journal:  J Physiol       Date:  1977-02       Impact factor: 5.182

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  5 in total

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Authors:  S Raucher; S E Dryer
Journal:  J Physiol       Date:  1994-08-15       Impact factor: 5.182

3.  Effects of caffeine and 3-isobutyl-1-methylxanthine on voltage-activated potassium currents in vertebrate neurones and secretory cells.

Authors:  M A Reiser; T D'Souza; S E Dryer
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4.  kappa- and mu-opioids reverse the somatostatin inhibition of Ca2+ currents in ciliary and dorsal root ganglion neurons.

Authors:  L Polo-Parada; G Pilar
Journal:  J Neurosci       Date:  1999-07-01       Impact factor: 6.167

5.  Regulation of A-currents by cell-cell interactions and neurotrophic factors in developing chick parasympathetic neurones.

Authors:  M M Dourado; S E Dryer
Journal:  J Physiol       Date:  1994-02-01       Impact factor: 5.182

  5 in total

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