Literature DB >> 8120828

Activation and inactivation of the bursting potassium channel from fused Torpedo synaptosomes.

J Edry-Schiller1, R Rahamimoff.   

Abstract

1. The voltage dependence of the bursting potassium channel in fused synaptosomes from Torpedo electric organ was studied in vitro, using the inside-out and the cell-attached configurations of the patch clamp technique. 2. The patch of membrane was held at various holding potentials (-140 to -50 mV) and then stepped to test potentials (-50 to +40 mV) for periods ranging from 5 to 300 ms. Each potential step was repeated 200-600 times. After subtraction of the capacitative transients and the leakage currents, an ensemble-averaged current was obtained. This ensemble current showed a marked activation upon depolarization, followed by an inactivation. 3. The activation of the bursting potassium channel is markedly dependent on the voltage step. Activation was detected at voltages positive to -50 mV. The peak of the ensemble current increases with the degree of depolarization, while the time to the peak decreases. With progressively larger depolarization, there is a shortening in the delay between the onset of the voltage step and the opening of the bursting potassium channels. 4. The inactivation phase of the ensemble current could be described adequately in most of the experiments, as a single exponential decay to a steady-state inactivation level. The time constant of inactivation was not markedly voltage dependent. 5. Single channel analysis of the inactivation reveals that it is due to a reduction in the number of channel openings and not due to changes in single channel current amplitude or channel mean open time along the pulse. 6. The holding potential has a marked effect on the peak amplitude of the ensemble current, indicating that hyperpolarization removes inactivation and depolarization induces it. The peak amplitude vs. voltage relation was fitted by the Boltzmann equation. The half-maximal inactivation was -105.2 +/- 5.8 mV (mean +/- S.E.M.), suggesting that at the resting potential a substantial fraction of the bursting potassium channels is in an inactivated state. 7. Two-pulse experiments show that the recovery from inactivation is a slow process which lasts well over 1 s. 8. High-frequency stimulation (20-66.7 Hz) by 5 ms pulses produces a progressive decline in the peak ensemble current amplitude. The decline is larger at higher stimulation frequencies.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8120828      PMCID: PMC1143982          DOI: 10.1113/jphysiol.1993.sp019921

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


  43 in total

1.  Biophysical and molecular mechanisms of Shaker potassium channel inactivation.

Authors:  T Hoshi; W N Zagotta; R W Aldrich
Journal:  Science       Date:  1990-10-26       Impact factor: 47.728

Review 2.  How might the diversity of potassium channels be generated?

Authors:  L Y Jan; Y N Jan
Journal:  Trends Neurosci       Date:  1990-10       Impact factor: 13.837

3.  A bursting potassium channel in isolated cholinergic synaptosomes of Torpedo electric organ.

Authors:  J Edry-Schiller; S Ginsburg; R Rahamimoff
Journal:  J Physiol       Date:  1991-08       Impact factor: 5.182

4.  Regulation of fast inactivation of cloned mammalian IK(A) channels by cysteine oxidation.

Authors:  J P Ruppersberg; M Stocker; O Pongs; S H Heinemann; R Frank; M Koenen
Journal:  Nature       Date:  1991-08-22       Impact factor: 49.962

5.  Action potential broadening and frequency-dependent facilitation of calcium signals in pituitary nerve terminals.

Authors:  M B Jackson; A Konnerth; G J Augustine
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-15       Impact factor: 11.205

Review 6.  Voltage-dependent potassium channels: minK and Shaker families.

Authors:  L K Kaczmarek
Journal:  New Biol       Date:  1991-04

7.  M-currents and other potassium currents in bullfrog sympathetic neurones.

Authors:  P R Adams; D A Brown; A Constanti
Journal:  J Physiol       Date:  1982-09       Impact factor: 5.182

8.  A fast, transient K+ current in neurohypophysial nerve terminals of the rat.

Authors:  P J Thorn; X M Wang; J R Lemos
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

9.  Nerve terminal excitability and neuromuscular transmission in T(X;Y)V7 and Shaker mutants of Drosophila melanogaster.

Authors:  A Mallart; D Angaut-Petit; C Bourret-Poulain; A Ferrús
Journal:  J Neurogenet       Date:  1991-02       Impact factor: 1.250

10.  Molecular basis of altered excitability in Shaker mutants of Drosophila melanogaster.

Authors:  R Lichtinghagen; M Stocker; R Wittka; G Boheim; W Stühmer; A Ferrus; O Pongs
Journal:  EMBO J       Date:  1990-12       Impact factor: 11.598

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  3 in total

Review 1.  Multitude of ion channels in the regulation of transmitter release.

Authors:  R Rahamimoff; A Butkevich; D Duridanova; R Ahdut; E Harari; S G Kachalsky
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

2.  The non-specific ion channel in Torpedo ocellata fused synaptic vesicles.

Authors:  N Yakir; R Rahamimoff
Journal:  J Physiol       Date:  1995-06-15       Impact factor: 5.182

3.  A-current modifies the spike of C-type neurones in the rabbit nodose ganglion.

Authors:  C Ducreux; J J Puizillout
Journal:  J Physiol       Date:  1995-07-15       Impact factor: 5.182

  3 in total

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