Literature DB >> 16992510

Chloride distribution in Aplysia neurones.

P Ascher1, D Kunze, T O Neild.   

Abstract

1. The intracellular Cl(-) concentration (Cl(i)) and the membrane potential (E(m)) were measured in the medial pleural neurones of Aplysia under various experimental conditions designed to determine the Cl(-) conductance of the neurones and investigate the possibility of an active Cl(-) transport.2. The magnitude of the Cl(-) conductance of the cell depends on the experimental conditions.3. In normal sea water, large changes of E(m) produced by passing current across the cell membrane caused no change of Cl(i), suggesting that the Cl(-) conductance was low. Similarly, moderate changes of E(Cl) produced by decreasing Cl(o) or increasing Cl(i) had little or no effect on E(m).4. A high Cl(-) conductance was observed in high K(o) or very low Cl(o). It was greatly reduced if the external Ca(2+) was replaced by Co(2+), or in the presence of tubocurarine, or if the experiment was performed on an isolated cell soma. The high Cl(-) conductance is therefore attributed to the release of ACh and perhaps other transmitters from synaptic terminals.5. High concentrations of tetraethylammonium ions or procaine induced a depolarization of the cell, but a decrease of Cl(i). The rate of fall of Cl(i) was increased by lowering external K(+) or raising external Ca(2+), and was decreased by replacing external Ca(2+) by Co(2+).6. NH(4) (+) ions applied externally had effects similar to those of K(+) ions. In situations in which intracellular NH(4) (+) might be increased a fall in Cl(i) was observed.7. The changes of Cl(i) caused by TEA, procaine, or internal NH(4) (+) occur against the driving force for passive Cl(-) movements. They are still observed in isolated cell bodies, and cannot be attributed to the activation of synaptic channels.8. Some interpretations of these anomalous Cl(-) movements are discussed which could also account for the difference between E(Cl) and E(m) observed under normal conditions.

Entities:  

Year:  1976        PMID: 16992510      PMCID: PMC1309315          DOI: 10.1113/jphysiol.1976.sp011332

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


  32 in total

1.  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

2.  The action of ammonium on postsynaptic inhibition of cat spinal motoneurons.

Authors:  H D Lux; C Loracher; E Neher
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

3.  Single presynaptic neurone mediates a two component postsynaptic inhibition.

Authors:  J Kehoe
Journal:  Nature       Date:  1969-03-01       Impact factor: 49.962

4.  Pharmacological characteristics and ionic bases of a 2 component postsynaptic inhibition.

Authors:  J Kehoe
Journal:  Nature       Date:  1967-09-30       Impact factor: 49.962

5.  [Modified electrical nature of giant axon membranes following the increase of external concentration of potassium ions].

Authors:  V D Gerasimov; P G Kostiuk; V A Maĭskiĭ
Journal:  Biofizika       Date:  1965

6.  The effect of ions on the membrane potential of snail neurones.

Authors:  G A Kerkut; R W Meech
Journal:  Comp Biochem Physiol       Date:  1967-02

7.  Ionic permeability of the inhibitory postsynaptic membrane of lobster muscle fibers.

Authors:  F Motokizawa; J P Reuben; H Grundfest
Journal:  J Gen Physiol       Date:  1969-10       Impact factor: 4.086

8.  Voltage clamp experiments in striated muscle fibres.

Authors:  R H Adrian; W K Chandler; A L Hodgkin
Journal:  J Physiol       Date:  1970-07       Impact factor: 5.182

9.  The ionic permeability changes during acetylcholine-induced responses of Aplysia ganglion cells.

Authors:  M Sato; G Austin; H Yai; J Maruhashi
Journal:  J Gen Physiol       Date:  1968-03       Impact factor: 4.086

10.  Increased chloride conductance as the proximate cause of hydrogen ion concentration effects in Aplysia neurons.

Authors:  A M Brown; R B Sutton; J L Walker
Journal:  J Gen Physiol       Date:  1970-11       Impact factor: 4.086

View more
  16 in total

1.  A zinc-dependent Cl- current in neuronal somata.

Authors:  T Tabata; A T Ishida
Journal:  J Neurosci       Date:  1999-07-01       Impact factor: 6.167

2.  Nonselective ionic channels in Aplysia neurones.

Authors:  D Chesnoy-Marchais; M G Evans
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

3.  Permeability, phase-boundary potential and conductance in a cholinergic channel without constant field.

Authors:  T L Schwartz; R T Kado
Journal:  Biophys J       Date:  1977-06       Impact factor: 4.033

4.  Modulation of transmission at an inhibitory synapse in the central nervous system of the leech.

Authors:  J Nicholls; B G Wallace
Journal:  J Physiol       Date:  1978-08       Impact factor: 5.182

5.  Continuous direct measurement of intracellular chloride and pH in frog skeletal muscle.

Authors:  T B Bolton; R D Vaughan-Jones
Journal:  J Physiol       Date:  1977-09       Impact factor: 5.182

6.  Liquid and solid-state Cl- -sensitive microelectrodes. Characteristics and application to intracellular Cl- activity in Balanus photoreceptor.

Authors:  J H Saunders; H M Brown
Journal:  J Gen Physiol       Date:  1977-10       Impact factor: 4.086

7.  The role of bicarbonate, chloride and sodium ions in the regulation of intracellular pH in snail neurones.

Authors:  R C Thomas
Journal:  J Physiol       Date:  1977-12       Impact factor: 5.182

8.  Endogenous Na(+)-K+ (or NH4+)-2Cl- cotransport in Rana oocytes; anomalous effect of external NH4+ on pHi.

Authors:  E Keicher; R Meech
Journal:  J Physiol       Date:  1994-02-15       Impact factor: 5.182

9.  Characterization of a chloride conductance activated by hyperpolarization in Aplysia neurones.

Authors:  D Chesnoy-Marchais
Journal:  J Physiol       Date:  1983-09       Impact factor: 5.182

10.  Genetically encoded optical sensors for monitoring of intracellular chloride and chloride-selective channel activity.

Authors:  Piotr Bregestovski; Tatyana Waseem; Marat Mukhtarov
Journal:  Front Mol Neurosci       Date:  2009-12-04       Impact factor: 5.639

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.