Literature DB >> 7097593

Effects of cholinergic drugs on receptive field properties of rabbit retinal ganglion cells.

M Ariel, N W Daw.   

Abstract

1. Retinal ganglion cells were recorded extracellularly from the rabbit's eye in situ to study the effects of cholinergic drugs on receptive field properties. Physostigmine, an acetylcholinesterase inhibitor, and nicotine increased the spontaneous activity of nearly all retinal ganglion cell types. The effectiveness of physostigmine was roughly correlated with the neurone's inherent level of spontaneous activity. Brisk cells, having high rates of spontaneous firing, showed large increases in their maintained discharge, whereas sluggish cells, with few or no spontaneous spikes, showed small and sometimes transient increases in spontaneous activity during physostigmine.2. The sensitivity of ganglion cells to spots of optimal size and position did not change substantially during the infusion of physostigmine. However, the responsiveness to light (number of spikes per stimulus above the spontaneous level) increased. This effect occurred with sluggish and more complex cells, rarely with brisk cells.3. Another effect of physostigmine on sluggish and more complex cells was to make these cells ;on-off'. The additional response to the inappropriate change in contrast had a long latency and lacked an initial transient burst.4. Complex receptive field properties such as orientation sensitivity, radial grating inhibition, speed tuning and size specificity were also examined. These inhibitory properties were still present during infusion of physostigmine and, in most cases, the trigger feature of each cell type remained.5. These results are consistent with pharmacological results on ACh release from the retina. There appear to be two types of release of ACh, having their most powerful influences on separate classes of cells. One release (transient), occurs at light onset and offset and acts primarily on sluggish and more complex ganglion cells; the other release (tonic) is not light-modulated and acts primarily on brisk cells. A wiring diagram for the ACh cells is suggested.

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Year:  1982        PMID: 7097593      PMCID: PMC1250697          DOI: 10.1113/jphysiol.1982.sp014104

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


  35 in total

1.  Properties of cat retinal ganglion cells: a comparison of W-cells with X- and Y-cells.

Authors:  J Stone; Y Fukuda
Journal:  J Neurophysiol       Date:  1974-07       Impact factor: 2.714

2.  Properties of rarely encountered types of ganglion cells in the cat's retina and an overall classification.

Authors:  B G Cleland; W R Levick
Journal:  J Physiol       Date:  1974-07       Impact factor: 5.182

3.  Brisk and sluggish concentrically organized ganglion cells in the cat's retina.

Authors:  B G Cleland; W R Levick
Journal:  J Physiol       Date:  1974-07       Impact factor: 5.182

4.  Neurotransmission in central nervous tissue: a study of isolated rabbit retina.

Authors:  A Ames; D A Pollen
Journal:  J Neurophysiol       Date:  1969-05       Impact factor: 2.714

5.  Comparison of the localization of acetylcholinesterase and non-specific cholinesterase activities in mammalian and avian retinas.

Authors:  C W Nichols; G B Koelle
Journal:  J Comp Neurol       Date:  1968-05       Impact factor: 3.215

6.  The effect of iontophoretically applied acetylcholine upon the cat's retinal ganglion cells.

Authors:  M Straschill; J Perwein
Journal:  Pflugers Arch       Date:  1973       Impact factor: 3.657

7.  Sampling properties of microelectrodes assessed in the cat's retina.

Authors:  J Stone
Journal:  J Neurophysiol       Date:  1973-11       Impact factor: 2.714

8.  Very slow-conducting ganglion cells in the cat's retina: a major, new functional type?

Authors:  J Stone; K P Hoffmann
Journal:  Brain Res       Date:  1972-08-25       Impact factor: 3.252

9.  Changes in the maintained discharge with adaptation level in the cat retina.

Authors:  H B Barlow; W R Levick
Journal:  J Physiol       Date:  1969-06       Impact factor: 5.182

10.  Receptive fields and trigger features of ganglion cells in the visual streak of the rabbits retina.

Authors:  W R Levick
Journal:  J Physiol       Date:  1967-02       Impact factor: 5.182

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  25 in total

1.  The nondiscriminating zone of directionally selective retinal ganglion cells: comparison with dendritic structure and implications for mechanism.

Authors:  S He; Z F Jin; R H Masland
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

2.  Synaptic connections of starburst amacrine cells and localization of acetylcholine receptors in primate retinas.

Authors:  Elizabeth S Yamada; Nina Dmitrieva; Kent T Keyser; Jon M Lindstrom; Louis B Hersh; David W Marshak
Journal:  J Comp Neurol       Date:  2003-06-16       Impact factor: 3.215

3.  Role of ACh-GABA cotransmission in detecting image motion and motion direction.

Authors:  Seunghoon Lee; Kyongmin Kim; Z Jimmy Zhou
Journal:  Neuron       Date:  2010-12-22       Impact factor: 17.173

4.  Stratification of α ganglion cells and ON/OFF directionally selective ganglion cells in the rabbit retina.

Authors:  Jian Zhang; Wei Li; Hideo Hoshi; Stephen L Mills; Stephen C Massey
Journal:  Vis Neurosci       Date:  2005 Jul-Aug       Impact factor: 3.241

Review 5.  The role of starburst amacrine cells in visual signal processing.

Authors:  W R Taylor; R G Smith
Journal:  Vis Neurosci       Date:  2012-01       Impact factor: 3.241

6.  Neurotransmission in the frog retina: possible physiological and histological correlations.

Authors:  N Bonaventure; B Jardon; J Sahel; N Wioland
Journal:  Doc Ophthalmol       Date:  1989-05       Impact factor: 2.379

Review 7.  Voltage-dependent conductances of solitary ganglion cells dissociated from the rat retina.

Authors:  S A Lipton; D L Tauck
Journal:  J Physiol       Date:  1987-04       Impact factor: 5.182

8.  Nicotinic and muscarinic acetylcholine receptors shape ganglion cell response properties.

Authors:  Christianne E Strang; Ye Long; Konstantin E Gavrikov; Franklin R Amthor; Kent T Keyser
Journal:  J Neurophysiol       Date:  2014-10-08       Impact factor: 2.714

9.  Synaptic transmission at N-methyl-D-aspartate receptors in the proximal retina of the mudpuppy.

Authors:  P D Lukasiewicz; J S McReynolds
Journal:  J Physiol       Date:  1985-10       Impact factor: 5.182

10.  Nicotinic acetylcholine receptor subunits in rhesus monkey retina.

Authors:  Ji Liu; Alice M McGlinn; Alcides Fernandes; Ann H Milam; Christianne E Strang; Margot E Andison; Jon M Lindstrom; Kent T Keyser; Richard A Stone
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-10-24       Impact factor: 4.799

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