Literature DB >> 5789945

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

H B Barlow, W R Levick.   

Abstract

1. The mean rate, impulse interval distribution, and pulse number distribution of the maintained discharge of ganglion cells in the retina of the cat have been studied after prolonged adaptation at different luminance levels.2. From a state of complete dark adaptation up to a luminance of about 5 x 10(-3) cd/m(2) (viewed through a 7 mm(2) pupil) the mean rate of on-centre units increases. From darkness up to a somewhat higher luminance the mean rate of some off-centre units decreases, but others show little change.3. Above 10(-2) cd/m(2) the mean rate ceases to show a regular relation with adaptation level. On units often decrease and then increase again at a higher level. Rhythmical fluctuations are common near 10(-2) cd/m(2), especially if the retina is not in first class condition. Mean rates above 70/sec and below 1/sec are very rare at any adaptation level.4. Over the range where mean rate increases monotonically with adaptation level, it is shown that the surround of on-centre units does not inhibit and off responses cannot be elicited. When the monotonic increase is slowed or reversed it becomes possible to elicit responses from the surround. We suspect that the surround exerts a sustained, tonic, inhibiting effect at higher adaptation levels, thus holding down the maintained discharge.5. There are rare units, forming less than 1% of those isolated, that show a regularly increasing frequency with increase of adaptation level above 10(-2) cd/m(2). These units have concentric ;on' and ;off' zones in their receptive fields, but the responses to rapidly changing stimuli are sluggish and they have an unusually regular maintained discharge. They have been tentatively called ;luminance units'.6. The impulse-interval and pulse-number distributions of on-centre units change predictably with adaptation level; the variance of the pulse number distribution is usually several times the mean at very low adaptation levels, but only a fraction of the mean at high levels. Off-centre units do not show predictable changes. Luminance units fire more regularly, and have narrower pulse-number and impulse interval distributions than other concentric units.7. A simple model is proposed to account for the statistical characteristics of the maintained discharge of on-centre units.

Mesh:

Year:  1969        PMID: 5789945      PMCID: PMC1351438          DOI: 10.1113/jphysiol.1969.sp008836

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


  16 in total

1.  An approach to the quantitative analysis of electrophysiological data from single neurons.

Authors:  G L GERSTEIN; N Y KIANG
Journal:  Biophys J       Date:  1960-09       Impact factor: 4.033

2.  [Spontaneous activity of individual fibers of the optic nerve of cats, and activity upon illumination. I. Influence of shortlasting retinal ischemia].

Authors:  H BORNSCHEIN
Journal:  Z Biol       Date:  1958-05

3.  Maintained activity in the cat's retina in light and darkness.

Authors:  S W KUFFLER; R FITZHUGH; H B BARLOW
Journal:  J Gen Physiol       Date:  1957-05-20       Impact factor: 4.086

4.  Increment thresholds at low intensities considered as signal/noise discriminations.

Authors:  H B BARLOW
Journal:  J Physiol       Date:  1957-05-23       Impact factor: 5.182

5.  Change of organization in the receptive fields of the cat's retina during dark adaptation.

Authors:  H B BARLOW; R FITZHUGH; S W KUFFLER
Journal:  J Physiol       Date:  1957-08-06       Impact factor: 5.182

6.  Discharge patterns and functional organization of mammalian retina.

Authors:  S W KUFFLER
Journal:  J Neurophysiol       Date:  1953-01       Impact factor: 2.714

7.  Three factors limiting the reliable detection of light by retinal ganglion cells of the cat.

Authors:  H B Barlow; W R Levick
Journal:  J Physiol       Date:  1969-01       Impact factor: 5.182

8.  [Statistical properties of neuron activity in the ascending visual system].

Authors:  A Herz; O Creutzfeldt; J Fuster
Journal:  Kybernetik       Date:  1964-06

9.  [The activity of neurones of the optic tract and of the lateral geniculate body during long lasting light stimuli of different intensity].

Authors:  M Straschill
Journal:  Kybernetik       Date:  1966-01

10.  Maintained activity of cat retinal ganglion cells.

Authors:  R W Rodieck
Journal:  J Neurophysiol       Date:  1967-09       Impact factor: 2.714

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  93 in total

1.  Negative interspike interval correlations increase the neuronal capacity for encoding time-dependent stimuli.

Authors:  M J Chacron; A Longtin; L Maler
Journal:  J Neurosci       Date:  2001-07-15       Impact factor: 6.167

2.  Effects of remote stimulation on the mean firing rate of cat retinal ganglion cells.

Authors:  C L Passaglia; C Enroth-Cugell; J B Troy
Journal:  J Neurosci       Date:  2001-08-01       Impact factor: 6.167

3.  A dopamine- and protein kinase A-dependent mechanism for network adaptation in retinal ganglion cells.

Authors:  C F Vaquero; A Pignatelli; G J Partida; A T Ishida
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

4.  Nonrenewal statistics of electrosensory afferent spike trains: implications for the detection of weak sensory signals.

Authors:  R Ratnam; M E Nelson
Journal:  J Neurosci       Date:  2000-09-01       Impact factor: 6.167

5.  Responses of single units in the monkey superior colliculus to stationary flashing stimuli.

Authors:  J Moors; A J Vendrik
Journal:  Exp Brain Res       Date:  1979-04-02       Impact factor: 1.972

6.  The control of retinal ganglion cell discharge by receptive field surrounds.

Authors:  C Enroth-Cugell; P Lennie
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

7.  Surround contribution to light adaptation in cat retinal ganglion cells.

Authors:  C Enroth-Cugell; P Lennie; R M Shapley
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

8.  Impact of noise on retinal coding of visual signals.

Authors:  Christopher L Passaglia; John B Troy
Journal:  J Neurophysiol       Date:  2004-04-07       Impact factor: 2.714

9.  Action and localization of gamma-aminobutyric acid in the cat retina.

Authors:  J Bolz; T Frumkes; T Voigt; H Wässle
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

10.  Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity.

Authors:  Hannah L Payne; Ranran L French; Christine C Guo; Td Barbara Nguyen-Vu; Tiina Manninen; Jennifer L Raymond
Journal:  Elife       Date:  2019-05-03       Impact factor: 8.140

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