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Biomedical subjects

C Blakemore

Publications and source records attributed to C Blakemore.

At least 109 records · Page 6Linked to original sources
PubMed1978

Physiological basis of anisometropic amblyopia.

In the visual cortex of kittens that have received their only visual experience while wearing a high-power lens before one eye, most neurons are dominated by input from the normal eye. Moreover, contrast sensitivity and resolving power are lower for stimulation through the originally defocused eye, mimicking psychophysical results from human anisometropic amblyopes.

Amblyopia↗
PubMed1978

Modification of the kitten's visual cortex by exposure to spatially periodic patterns.

Kittens were dark-reared except for exposure to three types of spatially periodic, vertically striped pattern: 1. single, widely spaced black bars; 2. wide areas of regular vertical grating separated by large blank patches; 3. a uniform, continuous grating with a spatial frequency of 0.5 c/deg. In each case there was a bias towards vertical in the distribution of preferred orientations of cells recorded in the visual cortex. The contrast sensitivity of individual neurones for gratings of different spatial frequencies was analysed quantitatively. In kittens exposed to a uniform grating of 0.5 c/deg, many cells were maximally sensitive close to 0.5 c/deg, as they are in normal cats. The occipital potential evoked by vertical gratings higher in frequency than 0.3 c/deg was consistently greater in amplitude than that for horizontal, and a vertical grating of 0.5 c/deg produced the maximum activity. These results are compared with those of Maffei and Fiorentini (1974); the differences between our results and theirs may be attributable to the degree of variability in spatial frequency and orientation during rearing, and to the duration of exposure.

Animals↗
PubMed1978

The physiological effects of monocular deprivation and their reversal in the monkey's visual cortex.

1. 1127 single units were recorded during oblique penetrations in area 17 of one normal, three monocularly deprived and four reverse sutured monkeys. 2. In all animals most cells outside layer IV c were orientation-selective, and preferred orientation usually shifted from cell to cell in a regular progressive sequence. 3. The presence in layer IV c of non-oriented, monocularly driven units, organized in alternating right-eye and left-eye 'stripes' (LeVay, Hubel & Wiesel, 1975) was confirmed. 4. Early monocular deprivation (2--5 1/2 weeks) caused a strong shift of ocular dominance towards the non-deprived eye. However, even outside layer IV c, neural background and some isolated cells could still be driven from the deprived eye in regularly spaced, narrow columnar regions. In layer IV c the non-deprived eye's stripes were almost three times wider, on average, than the deprived. 5. Later monocular deprivation (11--16 months) had no detectable influence on layer IV c but seemed to cause a small shift in ocular dominance outside IV c. Deprivation for 6 1/4 months in an adult had no such effect. 6. After early reverse suturing (at 5 1/2 weeks) the originally deprived eye gained dominance over cells outside layer IV c just as complete as that originally exercised by the eye that was first non-deprived. 7. The later reverse suturing was delayed, the less effective was recapture by the originally deprived eye. Reversal at 8 weeks led to roughly equal numbers of cells being dominated by each eye; fewer cells became dominated by the newly open eye after reverse suturing at 9 weeks and most of them were non-oriented; reversal at 38 1/2 weeks had no effect. 8. Binocular cells, though rare in reverse sutured animals, always had very similar preferred orientations in the two eyes. The columnar sequences of preferred orientation were not interrupted at the borders of ocular dominance columns. 9. Even within layer IV c there was evidence for re-expansion of physiologically determined ocular dominance stripes. After early reverse suture, stripes for the two eyes became roughly equal in width. Possible mechanisms for these changes are discussed.

Action Potentials↗
PubMed1977

An attempt to assess the effects of monocular deprivation and strabismus on synaptic efficiency in the kitten's visual cortex.

The relative effectiveness of the two eyes in exciting cells in the visual cortex was assessed, using both natural stimulation and electrical stimulation of the optic discs. It is is argued that supramaximal electrical stimulation of the optic nerve could possibly reveal 'subliminal' synaptic inputs even after monocular deprivation or artificial strabismus has caused a loss of natural input from that eye, if such 'silent' synaptic input still survives. However, in kittens monocularly deprived for various periods of time or made artificially strabismic, there was usually excellent agreement between the relative visual excitability in the two eyes and their relative electrical excitability. In one animal, monocularly deprived continuously until 23 weeks of age, we examined the effect of reversibly turning off signals from the normal eye by pressure blinding. There was no evidence of a very rapid return of sensitivity to either electrical or natural stimulation of the deprived eye.

Animals↗
PubMed1977

Uptake of horseradish peroxidase by geniculo-cortical axons in the golden hamster: analysis by computer reconstruction.

Micro-injections of horseradish peroxidase (HRP) were made into the visual cortex of the golden hamster. The "projection lines" of labelled neurons in the dorsal lateral geniculate nucleus (LGNd) were three-dimensionally reconstructed, using a computer graphics technique. The lines run rostrally and medially from their origins at the lateral surface of the nucleus. Using an anatomically determined retinotopic map of the LGNd, the positions of all labelled cells near the lateral surface were converted into equivalent visual field co-ordinates and displayed on a physiologically determined retinotopic map of the primary visual cortex. Comparison between the scatter of these equivalent retinotopic loci and an actual reconstruction of the injection site revealed that: 1. there was general agreement between the independent retinotopic maps of LGNd and visual cortex; 2. there was greater retinotopic scatter of labelled LGNd cells than could be accounted for by the area of tissue injury in the cortex; 3. the retinotopic scatter matched more closely the total visible halo of HRP staining in the grey matter; 4. HRP can be taken up from a cytoarchitectonic field into which it diffuses after injection into a neighbouring area; 5. HRP is probably not taken up by undamaged axons in the white matter. These results are compared with those obtained in other animals and other systems. No general rules emerge, but the possibility of uptake from wide areas of diffusion must be considered when interpreting results of HRP injection.

Animals↗
PubMed1977

The effects of monocular deprivation on different neuronal classes in the lateral geniculate nucleus of the cat.

Retrograde axonal transport of horseradish peroxidase (HRP) was used to identify two populations of cells in the lateral geniculate nucleus (LGN) of the cat. HRP was injected into area 17 and 18 separately in the same animals, and the neuronal somata giving rise to thalamo-cortical axons, identified by the presence of granular HRP reaction product within them, were measured. The mean size of LGN neurones labelled by injections in area 17 ("17-relay" cells) was less than of neurones filled from area 18 ("18-rely" cells). Similar separate injections into area 17 and 18 of monocularly deprived kittens also showed that in non-deprived LGN laminae 17-relay cells were, on average, smaller than 18-relay cells. In deprived laminae, 17-relay cells were some 20% smaller than in non-deprived laminae, but deprived 18-relay cells were 50-60% smaller than normal, being on average, actually smaller than deprived 17-relay cells. We conclude that the population of large LGN neurones projecting to area 18 is more severely affected by monocular deprivation than the smaller neurones projecting to area 17, and discuss the relationship of the morphological results to physiologically defined X and Y cells in the LGN.

Animals↗
PubMed1977

Monocular deprivation: morphological effects on different classes of neurons in the lateral geniculate nucleus.

Retrograde axonal transport of horseadish peroxidase from areas 17 and 18 of the cat's visual cortex labels, principally, the small (X) and large (Y) cells, respectively, of the lateral geniculate nucleus. Quantitative analysis of the sizes of these morphologically identified neurons after monocular deprivation shows that the arrest of cell growth in the deprived laminae involves mainly Y cells.

Animals↗
PubMed1976

Regional specialization in the golden hamster's retina.

Ganglion cell swere counted and measured in whole mounts of the hamster's retina, stained with methylene blue. Their density varies between about 1,000/mm2 at the edge of the retina to about 5-6,000/mm2 in a broad area centralis centred about 1.9 mm(39 deg) directly temporal to the optic disk. Maps of cell density show a long horizontal extension of the dense area in the nasal direction. The sizes of ganglion cell somata fall into two main groups--small cells (5-11 mum diameter) and large cells (greater than 11 mum), the latter including a small proportion of giant cells (greater than 17 mum). All three classes of cells are maximal in density in the area centralis, although the small cells are relatively more numerous there. The total number of cells is about 114,000 with about 63,000 small cells and about 51,000 large. The optic nerve contains about 69,000 unmyelinated axons and about 50,000 myelinated axons, suggesting that the latter are the fibres of the larger ganglion cells. It is likely that the projections of the centres of the areae centrales of the two eyes are normally divergent in space; they are therefore not on "corresponding retinal points."

Animals↗
PubMed1976

Functional organization in the visual cortex of the golden hamster.

The visual cortex of the golden hamster was studied by means of multi-unit and single unit recording, which revealed three separate retinotopic maps of the visual field in the posterior cortex. V1, corresponding to cyto-architectonic area 17, has the contralateral temporal field represented medially, the central visual field (extending about 10 deg ipsilateral) represented laterally and the lower field anteriorly. The borders of the map, especially for the upper field, seem to be more restricted than the whole visual field available to the contralateral hemiretina: V1 probably does not represent the extreme periphery of the field. A large fraction of V1 has binocular input, for up to about 50 deg lateral to the vertical midline. There is a retinotopic reversal near the representation of the vertical midline where V1 meets V2 (corresponding to the more lateral "area 18a"). There is another retinotopic reversal at the extremity of the contralateral field representation, where V1 meets Vm (the medial visual area, corresponding to "area 18"). V2 and Vm each contain a reduced mirror image version of the map in V1. Almost all isolated single units in V1 have receptive fields that can be classified as radially symmetrical (60%) or asymmetrical (35%). Symmetrical fields have ON (13%), OFF (4%), ON-OFF (30%) or "SILENT" (12%) central areas when plotted with flashing spots. There are minor but not striking differences between these groups in their field sizes, velocity preferences and so on. They almost invariably prefer moving to stationary stimuli but are not selective for orientation or direction of movement. Asymmetrical fields are of four types, three of which (type 1, 11%; type 2, 17%; and type 3, 2%) are orientation selective and resemble simple, complex and hypercomplex cells in the cat cortex. Some of these have direction as well as orientation preference. Axial movement detectors (5%) have a selectivity for one axis of motion, and thus prefer one orientation of edge, but respond equally well to movement of a spot. Vertical and horizontal orientation preferences, especially the latter, are much the most common. There is some evidence of clustering of cells according to receptive field type and, possibly, preferred orientation. Asymmetrical cells are, relatively somewhat rarer in the deeper cortical layers. Within the binocular segment, fully 89% of cells are binocularly driven and the receptive fields are similar in the two eyes. Receptive fields tend to increase in size away from the area centralis representation and, in a complementary fashion, the magnification factor decreases from up to 0.1 mm/deg at the area centralis representation to about 0.02 mm/deg for the peripheral field.

Animals↗
PubMed1976

Functional organization in the superior colliculus of the golden hamster.

The superior colliculus of the golden hamster was investigated by means of multi-unit and single unit recording. The retinotopic map, which probably embraces a projection from the entire retina of the contralateral eye, is organized as in other vertebrates, with the central field represented in the anterior colliculus, the upper field medially. Magnification factor is fairly uniform and is about 0.02 mm/deg. There is a small binocular segment (where almost half of all neurones have input from the ipsilateral eye) in the anterior colliculus, representing the area of field around the area centralis and the anterior pole of the field. In the more superficial layers, units have small (about 10 deg diameter) receptive fields, which can be classified as symmetrical, responding to slow movement (80%), very fast movement detectors (6%), directional movement detectors (13%) and axial movement detectors (1%). In the deeper layers, below the stratum opticum, receptive field size increases dramatically and many cells habituate rapidly, making them sensitive only to new events. Receptive fields can be classified as movement detectors (89%), directional movement detectors (10%) and axial movement detectors (2%). All directional receptive fields, at least in the upper visual field, have an upward component in their directional preferences. About 42% of deeper layer cells have somatic sensory input, responding to light touch on the fur or whiskers of the contralateral half of the body. Some 5% of cells respond to complex sounds on the contralateral side of the animal. Many of these somatic and auditory cells also have visual receptive fields and, throughout the colliculus, there is general correspondence between the maps of visual space, auditory space and the body surface. This correlation may be important in the regulation of orienting behaviour towards novel peripheral stimuli.

Animals↗