Literature DB >> 6707974

Spatial contrast adaptation characteristics of neurones recorded in the cat's visual cortex.

D G Albrecht, S B Farrar, D B Hamilton.   

Abstract

Spatial contrast adaptation, produced by prolonged exposure to high contrast grating patterns, has become an important psychophysical method for isolating spatial and orientation selective channels in the human visual system. It has been reasonably argued that this adaptation may be fundamentally dependent upon the activity of neurones in the striate cortex. To test the validity of this hypothesis, and several others, we measured the general adaptation characteristics of 144 striate neurones using a stimulus protocol comparable to the typical psychophysical methods. In general, during prolonged high contrast stimulation, the responses of most cells exponentially decayed from a transient peak response to a sustained plateau response; following adaptation, the responses to lower contrasts were depressed relative to the unadapted state but then gradually recovered from the transient depression to a sustained plateau. Such adaptation was a property common to both simple and complex cells (the distributions of the quantitative of adaptation were overlapping); there were however small but reliable differences. We compared the neurophysiological contrast adaptation with two psychophysical estimates of human contrast adaptation (threshold contrast elevation and apparent contrast reduction) and found that the time courses and the magnitudes were quite similar. The effect of contrast adaptation on the spatial frequency tuning was assessed by measuring the contrast response function at several different test spatial frequencies before and after adaptation at the optimum centre frequency. We found that the effect of adaptation decreased as the difference between test and adaptation frequency increased. Grating contrast adaptation has been alternatively described as 'constructive gain control' on the one hand and as 'deleterious fatigue' on the other. We tested the effect of contrast adaptation on the contrast response function and found (a) that adaptation shifts the curves vertically downward parallel to the response axis (thus reflecting a decrease in the maximum rate of firing and a deleterious compression of the response range) and (b) that adaptation shifts the curves horizontally to the right parallel to the contrast axis (thus reflecting a true sensitivity shift of the remaining response range for constructive maintenance of high differential sensitivity around the prevailing background level).(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6707974      PMCID: PMC1199473          DOI: 10.1113/jphysiol.1984.sp015092

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


  38 in total

1.  The impulses produced by sensory nerve-endings: Part II. The response of a Single End-Organ.

Authors:  E D Adrian; Y Zotterman
Journal:  J Physiol       Date:  1926-04-23       Impact factor: 5.182

2.  Orientation specificity and spatial selectivity in human vision.

Authors:  J A Movshon; C Blakemore
Journal:  Perception       Date:  1973       Impact factor: 1.490

3.  Receptive fields and functional architecture of monkey striate cortex.

Authors:  D H Hubel; T N Wiesel
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

4.  Adaptation in a vertebrate retina: intracellular recording in Necturus.

Authors:  F S Werblin
Journal:  J Neurophysiol       Date:  1971-03       Impact factor: 2.714

5.  On the existence of neurones in the human visual system selectively sensitive to the orientation and size of retinal images.

Authors:  C Blakemore; F W Campbell
Journal:  J Physiol       Date:  1969-07       Impact factor: 5.182

6.  Human cone saturation as a function of ambient intensity: a test of models of shifts in the dynamic range.

Authors:  D C Hood; T Ilves; E Maurer; B Wandell; E Buckingham
Journal:  Vision Res       Date:  1978       Impact factor: 1.886

7.  Detection thresholds for stimuli in humans and monkeys: comparison with threshold events in mechanoreceptive afferent nerve fibers innervating the monkey hand.

Authors:  V B Mountcastle; R H LaMotte; G Carli
Journal:  J Neurophysiol       Date:  1972-01       Impact factor: 2.714

8.  The perceived spatial frequency shift: evidence for frequency-selective neurones in the human brain.

Authors:  C Blakemore; J Nachmias; P Sutton
Journal:  J Physiol       Date:  1970-10       Impact factor: 5.182

9.  Intracellular recordings from gecko photoreceptors during light and dark adaptation.

Authors:  J Kleinschmidt; J E Dowling
Journal:  J Gen Physiol       Date:  1975-11       Impact factor: 4.086

10.  Adaptation in skate photoreceptors.

Authors:  J E Dowling; H Ripps
Journal:  J Gen Physiol       Date:  1972-12       Impact factor: 4.086

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  79 in total

1.  Temporal contrast adaptation in the input and output signals of salamander retinal ganglion cells.

Authors:  K J Kim; F Rieke
Journal:  J Neurosci       Date:  2001-01-01       Impact factor: 6.167

2.  Nonlinear temporal dynamics of the cerebral blood flow response.

Authors:  K L Miller; W M Luh; T T Liu; A Martinez; T Obata; E C Wong; L R Frank; R B Buxton
Journal:  Hum Brain Mapp       Date:  2001-05       Impact factor: 5.038

3.  Contrast gain control in the visual cortex: monocular versus binocular mechanisms.

Authors:  A M Truchard; I Ohzawa; R D Freeman
Journal:  J Neurosci       Date:  2000-04-15       Impact factor: 6.167

4.  Cellular mechanisms of long-lasting adaptation in visual cortical neurons in vitro.

Authors:  M V Sanchez-Vives; L G Nowak; D A McCormick
Journal:  J Neurosci       Date:  2000-06-01       Impact factor: 6.167

5.  Membrane mechanisms underlying contrast adaptation in cat area 17 in vivo.

Authors:  M V Sanchez-Vives; L G Nowak; D A McCormick
Journal:  J Neurosci       Date:  2000-06-01       Impact factor: 6.167

6.  Membrane potential and firing rate in cat primary visual cortex.

Authors:  M Carandini; D Ferster
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

7.  Temporal contrast adaptation in salamander bipolar cells.

Authors:  F Rieke
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

8.  Adaptation to temporal contrast in primate and salamander retina.

Authors:  D Chander; E J Chichilnisky
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

9.  Selective adaptation to color contrast in human primary visual cortex.

Authors:  S A Engel; C S Furmanski
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

10.  Context-dependent adaptive coding of interaural phase disparity in the auditory cortex of awake macaques.

Authors:  Brian J Malone; Brian H Scott; Malcolm N Semple
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

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