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The primary focus of this paper is the abrupt transition that occurs midway through the rhesus lateral geniculate nucleus (LGN) from six layers posteriorly (conventionally numbered 1-6, ventral to dorsal) to four layers anteriorly. At this transition, layers 4 and 6 fuse into a single layer, as do layers 3 and 5, requiring an inversion of the stacking order of the cell categories making up layers 4 and 5. To understand the topology of this transition and its relationship to geniculate retinotopy, we have created a functional atlas of a rhesus LGN that affords three-dimensional views of morphology and retinotopy at a resolution of 25 microm. The projection of the path of the transition into visual space is highly biased toward lower visual fields, intersecting the upper vertical meridian at 6.4 degrees , the horizonal meridian at 15.4 degrees, and the lower vertical meridian at 25.0 degrees. Between inclinations of -31 degrees and 55 degrees, layers 3 and 5 merge through an elongated tear in layer 4 that subsumes the optic disk gap and extends medially and laterally; elsewhere, layers 4 and 6 merge through a tear in layer 5. These tears cause substantial violations of retinotopy and laminar integrity, so the inversion of layers 4 and 5 requires that the forces establishing retinotopy and grouping by cell class be locally overcome during morphogenesis. The transition and associated tears are evaluated in the context of recent computational models of geniculate morphogenesis. We have also used the atlas to estimate the borders of the binocular (55 approximately 62 degrees) and monocular (91 approximately 97 degrees) visual fields. Files containing the atlas are made publicly available on a website.

Stimulation of the somatosensory system is more likely to evoke pain in patients with chronic pain after nervous system injury than in patients without somatosensory abnormalities. We now describe results of stimulation through a microelectrode at microampere thresholds (threshold microstimulation; TMIS) in the region of the human thalamic principal sensory nucleus (ventral caudal; Vc) during operations for treatment of movement disorders or of chronic pain. Patients were trained preoperatively to use a standard questionnaire to describe the location (projected field) and quality of sensations evoked by TMIS intraoperatively. The region of Vc was divided on the basis of projected fields into areas representing the part of the body where the patients experienced chronic pain (pain affected) or did not experience chronic pain (pain unaffected) and into a control area located in the thalamus of patients with movement disorders and no experience of chronic pain. The region of the Vc was also divided into a core region and a posterior-inferior region. The core was defined as the region above a standard radiologic horizontal line (anterior commissure-posterior commissure line; ACPC line) where the majority of cells responded to innocuous somatosensory stimulation. The posterior-inferior area was a cellular area posterior and inferior to the core. In both the core and the posterior-inferior regions, the proportion of sites where TMIS evoked pain was larger in pain-affected and unaffected areas than in control areas. The number of sites where thermal (warm or cold) sensations were evoked was correspondingly smaller, so that the total of pain-plus-thermal (sensation of warmth or cold) sites was the same in all areas. Therefore, sites pain where stimulation evoked pain in patients with neuropathic pain (i.e., pain following an injury to the nervous system) may correspond to sites where thermal sensations were evoked by stimulation in patients without somatosensory abnormality.

The laminar morphology and electrophysiologically determined retinotopic organization of a single rhesus macaque lateral geniculate nucleus (LGN) were reconstructed on series of coronal, sagittal, and horizontal cuts through a three-dimensional computer representation of the nucleus. Neurons were counted in this same nucleus, allowing the magnification functions (cells/degree2 as functions of eccentricity) of magnocellular and parvocellular layers to be determined after eliminating the effects of nonuniform volume shrinkage. Parvocellular magnification was approximately 10,000 times higher in the foveola than in the far periphery. On average, magnocellular neurons made up 2.6% of the LGN in the central 2 degrees (but probably a smaller fraction in the central fovea). The magnocellular portion increased steadily with eccentricity to 27% in the far periphery. Thus the magno/parvo ratio increases from foveola to far periphery by a factor of at least 14. The parvocellular magnification function matches estimates of cortical magnification, whereas the density of magnocellular afferents to cortex increases monotonically with eccentricity. At the posterior pole of the nucleus, the numbers of layers are reduced through a fusion of two layers and the disappearance of one or two others, a feature that may be associated with the foveal ipsilateral hemifield representation.

The response properties of neurons in the region of striate cortex subserving central retina (0 degrees-2 degrees) and in a region of representation of parafoveal retina (4 degrees-7 degrees) were studied in unanesthetized paralyzed macaque monkeys. Neurons sensitive to the orientation of the stimulus in the visual field (simple, complex, and hypercomplex), and neurons lacking orientation selectivity (concentric, and a new class termed uniform) were found. In foveal cortex non-oriented cells were more numerous, and orientation sensitive cells had less strict spatial stimulus requirements than in parafoveal cortex. Most neurons received a monocular input, either exclusively or very predominantly. Three types of neurons were recognized on the basis of their responses to chromatic stimuli. (1) Luminosity neurons (about half the population) gave the same qualitative response to all effective wayelengths and had a spectral sensitivity similar to that of the macaque, determined behaviorally. Cells with all spatial types of receptive fields, except simple, occurred in this group. (2) Spectrally-treated neurons also responded in the same manner to different wavelengths, but over a narrower range than luminosity neurons, and their maximal sensitivity was shifted toward one or the other end of the visible spectrum. All tuned neurons had uniform or complex receptive field. (3) Spectrally-opponent neurons were either excited or inhibited by long wavelengths and responded in the opposite manner to short wavelengths. For cells with uniform or complex receptive fields the two opponent systems were coextensive. Simple or concentric neurons often had dual-opponent organization. The distribution of functional types among different cortical layers was similar in parafoveal and foveal cortex. The functional attributes of ocular dominance and orientation sensitivity were found to be statistically independent dimensions of cortical organization. On the other hand, the correlation between spatial and chromatic properties did not vary between different cytoarchitectonic layers, a finding suggesting that these neuronal properties depend on conjoined projectional and intracortical connecting mechanisms.

Microelectrode recording techniques were used to investigate the projection of the visual field into the lateral geniculate nucleus (LGN) of Macaca mulatta. The data were used to construct charts plotting visual direction, designated in terms of azimuth and elevation, onto sections of the nucleus cut in coronal, sagittal and horizontal Horsley-Clarke planes. The projection of the horizontal meridian divides the LGN along its plane of symmetry into a medial-superior half having negative elevations and a lateral-inferior half having positive elevations. Elevations become more positive or negative with distance from this plane. Azimuths closest to the vertical meridian are located posteriorly, while the most peripheral azimuths are found at the anterior pole. Two families of surfaces representing visual directions of constant azimuth and elevation are described. Visual field zones of increasing eccentricity are represented serially along the posterior-anterior axis of the LGN, with the foveal area restricted to the posterior pole and the monocular crescent projecting to the anterior pole. The mapping is completely continuous across the horizontal meridian. The edges of the stacked cell laminae exposed around the periphery of the LGN form an oval band which receives the projection of the perimeter of the contralateral hemifield. The vertical meridian is represented by the posterior two-thirds of this band, while the periphery of the hemifield projects to the anterior third. The central visual field out to the optic disc is represented by six cell layers, while the rest of the binocular field projects to four layers only (2 parvocellular and 2 magnocellular). The monocular crescent is represented by one parvocellular and one magnocellular layer. Features associated with the projection column of the optic disc are integrated into the transition from six to four layers. Details of the receptive field topography in the vicinity of the optic disc discontinuities indicate that these gaps are produced by intralaminar mechanisms. The magnification factor (mm-3/steradian) increased monotonically from peripheral visual fields to the foveal center, varying over a range of three decades. This range is intermediate between those derived from data reported in the literature for the retina and the striate cortex. The ratio of LGN magnifications at any two angular eccentricities is a power function, with an exponent of 1.34, of the corresponding ratio of retinal ganglion cell densities. Similarly, the ratio of cortical magnifications (mm-2/steradian) at any two eccentricites is a power function, with an exponent of 1.35, of the corresponding ratio of LGN magnifications.