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Orientation column

About: Orientation column is a research topic. Over the lifetime, 1142 publications have been published within this topic receiving 130169 citations.


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Journal ArticleDOI
TL;DR: In locally anesthetized cats, extracellular recordings were made from single neurons in the lateral cruciate gyrus of cerebral cortex, indicating that the low-threshold system to motor cortex utilizes extracerebellar pathways including medial lemniscus and is facilitated by dentate nucleus.
Abstract: 1. In locally anesthetized cats, extracellular recordings were made from single neurons in the lateral cruciate gyrus of cerebral cortex. These neurons responded to natural activation of stretch re...

103 citations

Journal ArticleDOI
TL;DR: Horseradish peroxidase was injected in relatively massive amounts to cover most, or portions, of opercular striate cortex in four macaques and it is argued that this group also includes the cells labelled in and around lateral hypothalamus and cerebral peduncle, and that as a whole the group constitutes a cholinergic counterpart of the diffusely projecting monoaminergic systems.
Abstract: Horseradish peroxidase (HRP) was injected in relatively massive amounts to cover most, or portions, of opercular striate cortex in four macaques. Absence of transcallosal or circumventricular labelling, plus discrete and consistent retrograde labelling in other areas in the four cases, assured the validity and specificity of the observations. Numerous labelled cells in regions directly bordering striate cortex, however, were excluded from the analysis because of the possibility of uptake consequent to physical diffusion. With this exception, all labelled cells were counted at roughly 2-mm intervals for one case with extensive unilateral injection of HRP. Even excluding the closely circumstriate population, the totals indicate that more than 30% of the afferent input to striate cortex arises from nongeniculate sources. Four areas of neocortex together make up about one-fourth of the total afferents: superior temporal sulcus 17.1%; inferior occipital area, 6.1%; intraparietal sulcus, 0.4%; and parahippocampal gyrus, 0.3%. Other areas projecting to striate cortex include claustrum, pulvinar, nucleus paracentralis, raphe system, locus coeruleus, and the nucleus basalis of Meynert. Cells of the latter were particularly striking with their very heavy uptake of HRP, and, even in cases of minimal effective injection, were scattered throughout an extensive area from the posterior edge of the globus pallidus passing rostrally beyond the chiasm and into the nucleus of the diagonal band. On the basis of their distribution and known cholinergic affinity, it is argued that this group also includes the cells labelled in and around lateral hypothalamus and cerebral peduncle, and that as a whole the group constitutes a cholinergic counterpart of the diffusely projecting monoaminergic systems. It seems possible that the basalis projection at first follows a fornical-subcallosal pathway to reach striate cortex via callosoperforant fibers.

102 citations

Journal ArticleDOI
12 Mar 2015-Nature
TL;DR: It is shown that cells with similar orientation preferences form large patches that span the vertical thickness of the retinorecipient layers in the mouse superior colliculus, a finding with implications for behavioural responses mediated by this brain centre.
Abstract: More than twenty types of retinal ganglion cells conduct visual information from the eye to the rest of the brain. Each retinal ganglion cell type tessellates the retina in a regular mosaic, so that every point in visual space is processed for visual primitives such as contrast and motion. This information flows to two principal brain centres: the visual cortex and the superior colliculus. The superior colliculus plays an evolutionarily conserved role in visual behaviours, but its functional architecture is poorly understood. Here we report on population recordings of visual responses from neurons in the mouse superior colliculus. Many neurons respond preferentially to lines of a certain orientation or movement axis. We show that cells with similar orientation preferences form large patches that span the vertical thickness of the retinorecipient layers. This organization is strikingly different from the randomly interspersed orientation preferences in the mouse’s visual cortex; instead, it resembles the orientation columns observed in the visual cortices of large mammals. Notably, adjacent superior colliculus orientation columns have only limited receptive field overlap. This is in contrast to the organization of visual cortex, where each point in the visual field activates neurons with all preferred orientations. Instead, the superior colliculus favours specific contour orientations within ~30° regions of the visual field, a finding with implications for behavioural responses mediated by this brain centre.

102 citations

Journal ArticleDOI
TL;DR: Visuotopic maps of foveal striate cortex have been obtained by means of single cell recordings from four hemispheres in two awake, behaving macaque monkeys, and were sufficiently compatible with one another that they could be combined into one.
Abstract: Visuotopic maps of foveal striate cortex have been obtained by means of single cell recordings from four hemispheres in two awake, behaving macaque monkeys. The numbers of successful separate striate penetration sites in the four hemispheres were 42, 58, 81, and 61, for a total of 242. The resolution of the maps is 10 min of visual angle, nearly an order of magnitude finer than previous maps. No striate receptive field center was found more than 5 min into the ipsilateral visual field. The four maps were sufficiently compatible with one another that they could be combined into one. There are only minor magnification differences between the right and left hemispheres and between the upper and lower quadrants. There is a vertical/horizontal magnification anisotropy of about 1.5:1 in central foveal cortex (0 to 20 min). The composite map can be approximated by the complex logarithmic equation, w = 7.7 * ln (x + iy + 0.33), where w is expressed in millimeters and x and y are expressed in degrees.

102 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20231
20223
20212
20208
20192
20189