Representation Of Visual Field Research Articles

Binocular Integration in the Mouse Lateral Geniculate Nuclei

SummaryA key task for the visual system is to combine spatially overlapping representations of the environment, viewed by either eye, into a coherent image. In cats and primates, this is accomplished in the cortex [1], with retinal outputs maintained as separate monocular maps en route through the lateral geniculate nucleus (LGN). While this arrangement is also believed to apply to rodents [2, 3], this has not been functionally confirmed. Accordingly, here we used multielectrode recordings to survey eye-specific visual responses across the mouse LGN. Surprisingly, while we find that regions of space visible to both eyes do indeed form part of a monocular representation of the contralateral visual field, we find no evidence for a corresponding ipsilateral representation. Instead, we find many cells that can be driven via either eye. These inputs combine to enhance the detection of weak stimuli, forming a binocular representation of frontal visual space. This extensive thalamic integration marks a fundamental distinction in mechanisms of binocular processing between mice and other mammals.

Impact of chiasma opticum malformations on the organization of the human ventral visual cortex.

Congenital malformations of the optic chiasm, such as enhanced and reduced crossing of the optic nerve fibers, are evident in albinism and achiasma, respectively. In early visual cortex the resulting additional visual input from the ipsilateral visual hemifield is superimposed onto the normal retinotopic representation of the contralateral visual field, which is likely due to conservative geniculo-striate projections. Counterintuitively, this organization in early visual cortex does not have profound consequences on visual function. Here we ask, whether higher stages of visual processing provide a correction to the abnormal representation allowing for largely normal perception. To this end we assessed the organization patterns of early and ventral visual cortex in five albinotic, one achiasmic, and five control participants. In albinism and achiasma the mirror-symmetrical superposition of the ipsilateral and contalateral visual fields was evident not only in early visual cortex, but also in the higher areas of the ventral processing stream. Specifically, in the visual areas VO1/2 and PHC1/2 no differences in the extent, the degree of superposition, and the magnitude of the responses were evident in comparison to the early visual areas. Consequently, the highly atypical organization of the primary visual cortex was propagated downstream to highly specialized processing stages in an undiminished and unchanged manner. This indicates largely unaltered cortico-cortical connections in both types of misrouting, i.e., enhanced and reduced crossing of the optic nerves. It is concluded that main aspects of visual function are preserved despite sizable representation abnormalities in the ventral visual processing stream.

Visual Circuits: Mouse Retina No Longer a Level Playing Field

Unlike humans, monkeys, or carnivores, mice are thought to lack a retinal subregion devoted to high-resolution vision; systematic analysis has now shown that mice encode visual space non-uniformly, increasing their spatial sampling of the binocular visual field.

Uniformity and diversity of response properties of neurons in the primary visual cortex: Selectivity for orientation, direction of motion, and stimulus size from center to far periphery

Although the primary visual cortex (V1) is one of the most extensively studied areas of the primate brain, very little is known about how the far periphery of visual space is represented in this area. We characterized the physiological response properties of V1 neurons in anaesthetized marmoset monkeys, using high-contrast drifting gratings. Comparisons were made between cells with receptive fields located in three regions of V1, defined by eccentricity: central (3-5°), near peripheral (5-15°), and far peripheral (>50°). We found that orientation selectivity of individual cells was similar from the center to the far periphery. Nonetheless, the proportion of orientation-selective neurons was higher in central visual field representation than in the peripheral representations. In addition, there were similar proportions of cells representing all orientations, with the exception of the representation of the far periphery, where we detected a bias favoring near-horizontal orientations. The proportions of direction-selective cells were similar throughout V1. When the center/surround organization of the receptive fields was tested with gratings with varying diameters, we found that the population of neurons that was suppressed by large gratings was smaller in the far periphery, although the strength of suppression in these cells tended to be stronger. In addition, the ratio between the diameters of the excitatory centers and suppressive surrounds was similar across the entire visual field. These results suggest that, superimposed on the broad uniformity of V1, there are subtle physiological differences, which indicate that spatial information is processed differently in the central versus far peripheral visual fields.

Il luogo logico dell'io entro la mappa cognitiva del Tractatus di Wittgenstein

Wittgenstein’s Tractatus has a tree-like form and requires a coherent topdown reading. Every remark has to be placed at specific point assigned to it on tree of Tractatus, starting from very first page containing a significant chain of seven cardinal propositions. The theme of solipsism and self can be elucidated by means of a cognitive map, where each proposition becomes a node on a hierarchical graph. In fact, difficulty in understanding group 5.6 on the limits of my is due to a consecutive reading of propositions 5.5571 / 5.6, 5.634 / 5.64, etc. As confirmed by a close philological examination of his diaries and of manuscript MS104, these erroneous combinations of remarks hide real development of Wittgenstein’s thinking. In contrast, cognitive tree shows that problem of limits of language and springs from a rigorous analysis of way in which logic fills world (line 5.1, 5.5, 5.6); that relationship between ego and does explain why solipsism and realism coincide (5.63, 5.64); that Wittgenstein’s elimination of any extra-logic a priori includes Kantian forms of phenomena (5.633, 5.634); and so on. Proposition 5.6331, with its picture showing a deceptive representation of visual field, reveals real focus, that is actual shape of field of vision (metaphor of phenomenological world). This is a much more remarkable problem than a supposed question about position of eye. Scholars and editors generally presume that Wittgenstein has drawn a picture (to dispute it) of an eye inside its own visual field. But that cannot be his theme and he never in fact drew such an absurd depiction, as examination of his handwritten drafts clearly reveals.

No blind alleys for blindsight: multiple active pathways into extrastriate cortex

Extra-striate visual area V5/MT has a central role in processing visual information about motion and binocular depth. Neuronal signals in V5/MT have been linked to the perception of direction of motion, 3D and structure from motion (Krug, 2004). V5/MT receives inputs from a number of cortical and subcortical structures. The main source of visual input is thought to come from the retina via the lateral geniculate nucleus (LGN), through primary visual cortex (V1) directly to MT or via secondary visual cortex (V2) (Ninomiya et al. 2011). However, there is also strong evidence for a direct pathway from the LGN to V5/MT (Sincich et al. 2004) (Fig. 1). Figure 1 A schematic diagram of some of the key feedforward pathways into primate V5/MT This pathway has been postulated to be of central importance for the remaining visual capacity in blindsight patients (Bridge et al. 2008). Patients with blindsight have lesions in V1, but can still discriminate high contrast moving stimuli seemingly without full awareness of the visual stimulus. The neural substrate for blindsight has also been investigated in monkeys with V1 lesions. A recent study blocking activity in the LGN underlined the importance of a direct pathway from the LGN to V5/MT to account for monkeys’ ability to discriminate visual stimuli within a V1 scotoma (Schmid et al. 2010). While such studies can provide evidence for the existence of the direct pathway, the question remains what functional significance this pathway has in healthy subjects. Recently, a human fMRI study suggested that voxels in human MT+ are more strongly correlated with voxels in the LGN than with voxels in V1 (Gaglianese et al. 2012). These data suggest that the direct LGN pathway could be an important driving force for neuronal responses in MT+. However, the result could also be influenced by the similar visual magnification factors in MT and LGN, while in V1 a similar extent of the visual field occupies generally a larger area of cortex, thereby diluting any correlation between voxels of the same size in the LGN and V1. A promising approach to understanding the contribution of the different pathways to visual processing is the functional dissection of the direct and indirect pathway as undertaken in a paper in this issue of The Journal of Physiology by Jayakumar et al. (2013). The LGN is subdivided in magno-, parvo- and koniocellular layers (Fig. 1); the neurons in each of these subcompartments show distinct response properties. Neurons in the magnocellular layers are selective for low spatial and high temporal frequencies and can respond to low contrast luminance stimuli. Neurons in the parvocellular layers preferentially respond to high spatial and low temporal frequencies and many are wavelength selective showing red–green opponency. Many neurons in the koniocellular layers are also wavelength selective showing blue-yellow opponency. Jayakumar and colleagues used S-cone isolating stimuli to selectively activate this latter pathway. They compared neuronal responses to these stimuli in visual area V5/MT before and after reversibly switching off the corresponding visual field representation in V1 through cooling. Even when visual stimuli were entirely presented in the centre of the visual field whose representation was inactivated in V1, neuronal responses in a number of neurons in V5/MT were not affected. This suggests that such neurons received their inputs through an alternative pathway that bypasses V1, presumably directly from the LGN. Conversely, the response of other V5/MT cells was affected. Taken together, this indicates that S-cone input reaches V5/MT through both pathways. Similar results were shown for luminance modulated stimuli. Interestingly, the timing of the responses in V5/MT for the indirect and direct pathways showed a large overlap. Conventionally, magnocellular inputs have been thought to dominate V5/MT responses serving the fast processing of visual motion information for quick action. A direct input from the LGN was thought to benefit such processing. The recent data on response times indicates that for each type of input, responses arrive through both pathways on overlapping time scales. The only partial abolition of responses in some V5/MT neurons by V1 cooling might be taken to indicate that both pathways feed into the same circuits. This underlines the functional importance of the direct pathway for preserving some visual function in blindsight. To probe deeper into the functional significance of the different pathways to V5/MT, experiments are required that selectively and reversibly alter activity in these distinct processing streams in the behaving animal.

Intrinsic signal optical imaging evidence for dorsal V3 in the prosimian galago (Otolemur garnettii).

Currently, we lack consensus regarding the organization along the anterior border of dorsomedial V2 in primates. Previous studies suggest that this region could be either the dorsomedial area, characterized by both an upper and a lower visual field representation, or the dorsal aspect of area V3, which only contains a lower visual field representation. We examined these proposals by using optical imaging of intrinsic signals to investigate this region in the prosimian galago (Otolemur garnettii). Galagos represent the prosimian radiation of surviving primates; cortical areas that bear strong resemblances across members of primates provide a strong argument for their early origin and conserved existence. Based on our mapping of horizontal and vertical meridian representations, visuotopy, and orientation preference, we find a clear lower field representation anterior to dorsal V2 but no evidence of any upper field representation. We also show statistical differences in orientation preference patches between V2 and V3. We additionally supplement our imaging results with electrode array data that reveal differences in the average spatial frequency preference, average temporal frequency preference, and sizes of the receptive fields between V1, V2, and V3. The lack of upper visual field representation along with the differences between the neighboring visual areas clearly distinguish the region anterior to dorsal V2 from earlier visual areas and argue against a DM that lies along the dorsomedial border of V2. We submit that the region of the cortex in question is the dorsal aspect of V3, thus strengthening the possibility that V3 is conserved among primates.

The Retinotopic Organization of Striate Cortex Is Well Predicted by Surface Topology

In 1918, Gordon Holmes combined observations of visual-field scotomas across brain-lesioned soldiers to produce a schematic map of the projection of the visual field upon the striate cortex. One limit to the precision of his result, and the mapping of anatomy to retinotopy generally, is the substantial individual variation in the size, volumetric position, and cortical magnification of area V1. When viewed within the context of the curvature of the cortical surface, however, the boundaries of striate cortex fall at a consistent location across individuals. We asked whether the surface topology of the human brain can be used to accurately predict the internal, retinotopic function of striate cortex as well. We used fMRI to measure polar angle and eccentricity in 25 participants and combined their maps within a left-right, transform-symmetric representation of the cortical surface. These data were then fit using a deterministic, algebraic model of visual-field representation. We found that an anatomical image alone can be used to predict the retinotopic organization of striate cortex for an individual with accuracy equivalent to 10-25 min of functional mapping. This indicates tight developmental linkage of structure and function within a primary, sensory cortical area.

Plasticity and Stability of the Visual System in Human Achiasma

The absence of the optic chiasm is an extraordinary and extreme abnormality in the nervous system. The abnormality produces highly atypical functional responses in the cortex, including overlapping hemifield representations and bilateral population receptive fields in both striate and extrastriate visual cortex. Even in the presence of these large functional abnormalities, the effect on visual perception and daily life is not easily detected. Here, we demonstrate that in two achiasmic humans the gross topography of the geniculostriate and occipital callosal connections remains largely unaltered. We conclude that visual function is preserved by reorganization of intracortical connections instead of large-scale reorganizations of the visual cortex. Thus, developmental mechanisms of local wiring within cortical maps compensate for the improper gross wiring to preserve function in human achiasma.

Heterogeneous auditory–visual integration: Effects of pitch, band-width and visual eccentricity

The identification of monosynaptic connections between primary cortices in non-human primates has recently been complemented by observations of early-latency and low-level non-linear interactions in brain responses in humans as well as observations of facilitative effects of multisensory stimuli on behavior/performance in both humans and monkeys. While there is some evidence in favor of causal links between early–latency interactions within low-level cortices and behavioral facilitation, it remains unknown if such effects are subserved by direct anatomical connections between primary cortices. In non-human primates, the above monosynaptic projections from primary auditory cortex terminate within peripheral visual field representations within primary visual cortex, suggestive of there being a potential bias for the integration of eccentric visual stimuli and pure tone (vs. broad-band) sounds. To date, behavioral effects in humans (and monkeys) have been observed after presenting (para)foveal stimuli with any of a range of auditory stimuli from pure tones to noise bursts. The present study aimed to identify any heterogeneity in the integration of auditory–visual stimuli. To this end, we employed a 3 × 3 within subject design that varied the visual eccentricity of an annulus (2.5°, 5.7°, 8.9°) and auditory pitch (250, 1000, 4000 Hz) of multisensory stimuli while subjects completed a simple detection task. We also varied the auditory bandwidth (pure tone vs. pink noise) across blocks of trials that a subject completed. To ensure attention to both modalities, multisensory stimuli were equi-probable with both unisensory visual and unisensory auditory trials that themselves varied along the abovementioned dimensions. Median reaction times for each stimulus condition as well as the percentage gain/loss of each multisensory condition vs. the best constituent unisensory condition were measured. The preliminary results reveal that multisensory interactions (as measured from simple reaction times) are indeed heterogeneous across the tested dimensions and may provide a means for delimiting the anatomo-functional substrates of behaviorally-relevant early–latency neural response interactions. Interestingly, preliminary results suggest selective interactions for visual stimuli when presented with broadband stimuli but not when presented with pure tones. More precisely, centrally presented visual stimuli show the greatest index of multisensory facilitation when coupled to a high pitch tone embedded in pink noise, while visual stimuli presented at approximately 5.7° of visual angle show the greatest slowing of reaction times.

Effects of healthy aging on human primary visual cortex.

Aging often results in reduced visual acuity from changes in both the eye and neural circuits [1-4]. In normally aging subjects, primary visual cortex has been shown to have reduced responses to visual stimulation [5]. It is not known, however, to what extent aging affects visual field representations and population receptive sizes in human primary visual cortex. Here we use functional MRI (fMRI) and population receptive field (pRF) modeling [6] to measure angular and eccentric retinotopic representations and population receptive fields in primary visual cortex in healthy aging subjects ages 57 - 70 and in healthy young volunteers ages 24 - 36 (n = 9). Retinotopic stimuli consisted of black and white, drifting checkerboards comprising moving bars 11 deg in radius. Primary visual cortex (V1) was clearly identifiable along the calcarine sulcus in all hemispheres. There was a significant decrease in the surface area of V1 from 0 to 3 deg eccentricity in the aging subjects with respect to the young subjects (p = 0.039). The coherence of the fMRI% BOLD modulation was significantly decreased in the aging subjects compared to the young subjects in the more peripheral eccentricity band from 7 to 10 deg (p = 0.029). Finally, pRF sizes were significantly increased within the 0 to 3 deg foveal representation of V1 in the aging subjects compared to the young subjects (p = 0.019). Understanding the extent of changes that occur in primary visual cortex during normal aging is essential both for understanding the normal aging process and for comparisons of healthy, aging subjects with aging patients suffering from age-related visual and cortical disorders.

The case for primate V3

The visual system in primates is represented by a remarkably large expanse of the cerebral cortex. While more precise investigative studies that can be performed in non-human primates contribute towards understanding the organization of the human brain, there are several issues of visual cortex organization in monkey species that remain unresolved. In all, more than 20 areas comprise the primate visual cortex, yet there is little agreement as to the exact number, size and visual field representation of all but three. A case in point is the third visual area, V3. It is found relatively early in the visual system hierarchy, yet over the last 40 years its organization and even its very existence have been a matter of debate among prominent neuroscientists. In this review, we discuss a large body of recent work that provides straightforward evidence for the existence of V3. In light of this, we then re-examine results from several seminal reports and provide parsimonious re-interpretations in favour of V3. We conclude with analysis of human and monkey functional magnetic resonance imaging literature to make the case that a complete V3 is an organizational feature of all primate species and may play a greater role in the dorsal stream of visual processing.

Functional Specialization of Seven Mouse Visual Cortical Areas

To establish the mouse as a genetically tractable model for high-order visual processing, we characterized fine-scale retinotopic organization of visual cortex and determined functional specialization of layer 2/3 neuronal populations in seven retinotopically identified areas. Each area contains a distinct visuotopic representation and encodes a unique combination of spatiotemporal features. Areas LM, AL, RL, and AM prefer up to three times faster temporal frequencies and significantly lower spatial frequencies than V1, while V1 and PM prefer high spatial and low temporal frequencies. LI prefers both high spatial and temporal frequencies. All extrastriate areas except LI increase orientation selectivity compared to V1, and three areas are significantly more direction selective (AL, RL, and AM). Specific combinations of spatiotemporal representations further distinguish areas. These results reveal that mouse higher visual areas are functionally distinct, and separate groups of areas may be specialized for motion-related versus pattern-related computations, perhaps forming pathways analogous to dorsal and ventral streams in other species.

New methods devised specify the size and color of the spots monkeys see when striate cortex (area V1) is electrically stimulated

Creating a prosthetic device for the blind is a central future task. Our research examines the feasibility of producing a prosthetic device based on electrical stimulation of primary visual cortex (area V1), an area that remains intact for many years after loss of vision attributable to damage to the eyes. As an initial step in this effort, we believe that the research should be carried out in animals, as it has been in the creation of the highly successful cochlear implant. We chose the rhesus monkey, whose visual system is similar to that of man. We trained monkeys on two tasks to assess the size, contrast, and color of the percepts created when single sites in area V1 are stimulated through microelectrodes. Here, we report that electrical stimulation within the central 5° of the visual field representation creates a small spot that is between 9 and 26 min of arc in diameter and has a contrast ranging between 2.6% and 10%. The dot generated by the stimulation in the majority of cases was darker than the background viewed by the animal and was composed of a variety of low-contrast colors. These findings can be used as inputs to models of electrical stimulation in area V1. On the basis of these findings, we derive what kinds of images would be expected when implanted arrays of electrodes are stimulated through a camera attached to the head whose images are converted into electrical stimulation using appropriate algorithms.

Transmission of colour and acuity signals by parvocellular cells in marmoset monkeys

The red-green axis of colour vision evolved recently in primate evolutionary history. Signals serving red-green colour vision travel together with signals serving spatial vision, in the parvocellular (PC) division of the subcortical visual pathway. However, the question of whether receptive fields of PC pathway cells are specialized to transmit red-green colour signals remains unresolved. We addressed this question in single-cell recordings from the lateral geniculate nucleus of anaesthetized marmosets. Marmosets show a high proportion of dichromatic (red-green colour-blind) individuals, allowing spatial and colour tuning properties of PC cells to be directly compared in dichromatic and trichromatic visual systems. We measured spatial frequency tuning for sine gratings that provided selective stimulation of individual photoreceptor types. We found that in trichromatic marmosets, the foveal visual field representation is dominated by red-green colour-selective PC cells. Colour selectivity of PC cells is reduced at greater eccentricities, but cone inputs to centre and surround are biased to create more selectivity than predicted by a purely 'random wiring' model. Thus, one-to-one connections in the fovea are sufficient, but not necessary, to create colour-selective responses. The distribution of spatial tuning properties for achromatic stimuli shows almost complete overlap between PC cells recorded in dichromatic and trichromatic marmosets. These data indicate that transmission of red-green colour signals has been enabled by centre-surround receptive fields of PC cells, and has not altered the capacity of PC cells to serve high-acuity vision at high stimulus contrast.

Refractive surgery in anisometropic adult patients induce plastic changes in primary visual cortex

To prospectively study the effect of refractive surgery in the primary visual cortex of adult anisometropic and isometropic myopic patients. Two anisometropic and two isometropic myopic patients were examined with multifocal functional magnetic resonance imaging technique (mffMRI) before refractive surgery and at 3, 6, 9 and 12 months postoperatively. Two controls without refractive surgery were also examined with mffMRI in the beginning and in the end of the study. Anisometropic patients had only their more myopic eye operated to correct the anisometropia. The myopic isometropic patients had their both eyes operated. Operated anisometropic eyes showed 65% reduced amount of active voxels in foveal data at 12 months postoperatively compared with the preoperative situation. In unoperated anisometropic eyes, the corresponding value was 86% and in myopic patients and controls 31% and 1%, respectively. To confirm this finding, the number of activated voxels representing the innermost ring of the stimulus was also calculated, and an exactly similar phenomenon was encountered in the anisometropic patients. Both anisometropic patients improved the best-spectacle-corrected visual acuity in the operated eye after refractive surgery. Our results suggest that plastic changes may take place in the primary visual cortex of anisometropic adult patients after refractive surgery.

Projections to Early Visual Areas V1 and V2 in the Calcarine Fissure from Parietal Association Areas in the Macaque

Non-extrastriate projections to area V1 in monkeys, now demonstrated by several anatomical studies, are potential substrates of physiologically documented multisensory effects in primary sensory areas. The full network of projections among association and primary areas, however, is likely to be complex and is still only partially understood. In the present report, we used the anterograde tracer biotinylated dextran amine to investigate projections to areas V1 and V2 from subdivisions of the parietal association cortex in macaque. Parietal cortex was chosen to allow comparisons between projections from this higher association area and from other previously reported areas. In addition, we were interested in further elucidating pathways to areas V1 and V2 from parietal areas, as potentially contributing to attention and active vision. Of eight cases, three brains had projections only to area V2, and the five others projected to both areas V1 and V2. Terminations in area V1 were sparse. These were located in supragranular layers I, II, upper III; occasionally in IVB; and in layer VI. Terminations in V2 were denser, and slightly more prevalent in the supragranular layers. For both areas, terminations were in the calcarine region, corresponding to the representation of the peripheral visual field. By reconstructions of single axons, we demonstrated that four of nine axons had collaterals, either to V1 and V2 (n = 1) or to area V1 and a ventral area likely to be TEO (n = 3). In area V1, axons extended divergently in layer VI as well as layer I. Overall, these and previous results suggest a nested connectivity architecture, consisting of multiple direct and indirect recurrent projections from association areas to area V1. Terminations in area V1 are not abundant, but could be potentiated by the network of indirect connections.

Self-organisation in the human visual system—Visuo-motor processing with congenitally abnormal V1 input

Due to an abnormal projection of the temporal retina the albinotic primary visual cortex receives substantial input from the ipsilateral visual field. To test whether representation abnormalities are also evident in higher tier visual, and in motor and somatosensory cortices, brain activity was measured with fMRI in 14 subjects with albinism performing a visuo-motor task. During central fixation, a blue or red target embedded in a distractor array was presented for 250ms in the left or right visual hemifield. After a delay, the subjects were prompted to indicate with left or right thumb button presses the target presence in the upper or lower hemifield. The fMRI responses were evaluated for different regions of interest concerned with visual, motor and somatosensory processing and compared to previously acquired data from 14 controls. The following results were obtained: (1) in albinism the hit rates in the visuo-motor task were indistinguishable from normal. (2) In area MT and the intraparietal sulcus there was an indication of abnormal lateralisation patterns. (3) Largely normal lateralisation patterns were evident in motor and somatosensory cortices. It is concluded that in human albinism, the abnormal visual field representation is made available for visuo-motor processing with a motor cortex that comprises an essentially normal lateralisation. Consequently, specific adaptations of the mechanisms mediating visuo-motor integration are required in albinism.

Retinotope Kartierung des menschlichen visuellen Kortex mit funktioneller Magnetresonanztomografie – Grundlagen, aktuelle Entwicklungen und Perspektiven für die Ophthalmologie

Since its initial introduction in the mid-1990s, retinotopic mapping of the human visual cortex, based on functional magnetic resonance imaging (fMRI), has contributed greatly to our understanding of the human visual system. Multiple cortical visual field representations have been demonstrated and thus numerous visual areas identified. The organisation of specific areas has been detailed and the impact of pathophysiologies of the visual system on the cortical organisation uncovered. These results are based on investigations at a magnetic field strength of 3Tesla or less. In a field-strength comparison between 3 and 7Tesla, it was demonstrated that retinotopic mapping benefits from a magnetic field strength of 7Tesla. Specifically, the visual areas can be mapped with high spatial resolution for a detailed analysis of the visual field maps. Applications of fMRI-based retinotopic mapping in ophthalmological research hold promise to further our understanding of plasticity in the human visual cortex. This is highlighted by pioneering studies in patients with macular dysfunction or misrouted optic nerves.

Functional MRI for patients with visual pathway diseases

Objective To observe the results of function MRI and perimetry in patients with visual pathway diseases. Methods Three patients (6 eyes) with pituitary adenoma and craniopharyngioma diagnosed via pathological examination and three healthy volunteers aged from 24 to 30 were collected. The best corrected visual acuity was non-light perception-1. 0 in the 6 sick eyes and 1. 0 in the healthy eyes;all the involved individuals had no other ocular diseases except myopia and without any contraindications of MRI. Common tests including the best visual acuity, fundus test by direct or indirect ophthalmoscope, center static visual field tested by Octopus 101 perimeter, program 32, tendency oriented perimetry were performed. The visual stimulation subtended a field of view of about 12 degrees,consisted of high contrast and drifting checkerboards. MRI parameters: GE signa VH/i 3. 0T scanner. Functional data: GRE-EPI sequence, 20 slices lying perpendicular to the calcarine sulcus. Anatomical data was obtained using 3DSPGR sequence to acquire high resolution. The cortical surface was unfolded and then cut and inflated. Functional data was presented to the inflated surface and subsequently analyzed by AFNI software. Results In six eyes, three had temporal defects, two had upper temporal visual field defects, and the other one did not finish the visual field test. The retinotopic representations of health adults were obtained by using the phase-encoded visual stimulation. The Eccentricity coordinate maps showed that foveal representations lay in the occipital poles and the representations appeared further anterior as eccentricity increased. The polar angle coordinate maps showed that early retinotopically organized areas had a representation of visual field. The visual cortex beneath the calcarine sulcus matched with the upper visual field of the opposite side and which upon the calcarine sulcus matched with the under visual field of the opposite side. Less or no visual cortex response was revealed in the patients' function MRI or the response in injury side was vanished. The visual cortex response related with the visual field defects could not be induced in function MRI. Conclusion There is a good correlation between function MRI data and the results of perimetric evaluation. The function MRI can show the visual cortex response correlated with the visual field defects of the patients with visual pathway diseases. Key words: Optic neuritis/diagnosis; Pituitary neoplasms/diagnosis; Craniopharyngioma/diagnosis; Magnetic resonance imaging/utilization; Perimetry/utilization