Biomedical subjects
Publications and source records attributed to L Maffei.
A square-wave grating from which the fundamental harmonic has been subtracted (missing fundamental grating) when viewed from a suitable distance appears similar to another grating of periodicity three times higher. The neurons of the visual cortex of the cat, in a given range of spatial frequencies characteristic of each cell, give similar responses to the two gratings.
1. The activity of neurones of the visual cortex (area 17) has been recorded in anaesthetized cats in response to gratings of different profile and to single light and dark bars. 2. At very low spatial frequencies, outside the frequency response range to sinusoidal gratings, the response to square-wave drifting gratings is obtainable from a combination of the response to the single bars of the grating presented in isolation. At higher spatial frequencies this is no longer true. 3. At very low spatial frequencies the responses to square-wave gratings and to missing-fundamental gratings (obtained by subtraction from the square-wave grating of its fundamental gratings (obtained by subtraction from the square-wave grating of its fundamental harmonic) are very similar. 4. At spatial frequencies near the peak of the spatial frequency tuning curve of the cell, the responses to square-wave grating and to sinusoidal gratings are very similar. At these spatial frequencies the response to the missing-fundamental grating is practically zero. 5. At spatial frequencies lower than that of best sensitivity for the cell, the response to square-wave gratings is correlated with the 1st and 3rd harmonic of the stimulus. 6. We conclude that at very low spatial frequencies of the grating the response of cortical cells is correlated with the light or dark edges (or light or dark bars) of the stimulus, because the edges contain high frequencies within the range of sensitivity of the cells. At higher spatial frequencies the results are interpreted best by assuming that cortical cells respond to the harmonics of the visual periodic stimulus. 7. When a background of dynamic visual noise is added to increase the spontaneous discharge of simple cells, their response to visual stimuli becomes linear or quasi-linear. The stimuli could be either single bars or gratings.
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We investigated the pathogenesis of isolated erythrocytosis of 14 yr duration in a 28-yr-old man. The increase in red cell mass was attributed to increased erythropoietin production. An extensive search for recognized causes of secondary erythrocytosis was unrevealing. Family members were found to be hematologically normal. After reduction of the circulating red cell mass by 20%, erythropoietin activity nearly quadrupled, thus suggesting a normal erythropoietin response to phlebotomy. When bone marrow cells of the patient were cultured in plasma clots in the absence of added erythropoietin, endogenous erythroid colony formation was observed, a pattern previously believed to be specific for polycythemia vera bone marrow cells. Our observations suggest that the erythrocytosis in this individual is best explained by an abnormal "servoregulatory" mechanism of erythropoietin production. In addition, this is the first instance in which the rule that endogenous erythroid colony formation is correlated with the diagnosis of polycythemia vera has not held.
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1. Kittens were exposed to a periodic grating orientated vertically during the critical period of their life. 2. At the end of the critical period the amplitude of the response to drifting gratings was found to be reduced at the spatial frequency of exposure in multi-unit and in some single unit recordings at lateral geniculate level. 3. The contrast sensitivity measured with behavioural methods also showed a depression at the spatial frequency of exposure. 4. An analysis of the preferred stimulus orientation of cortical units in area 17 showed that all orientations were represented.
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Electrical stimulation of the intraorbital part of the motor branches of extraocular muscles, where proprioceptive fibers run, evokes responses in 25% of the units of the striate cortex of the cat. The latency ranges between 25 and 40 msec. Mechanical stretch of extraocular muscles evokes multiunit responses in the striate cortex. The response is abolished by injection of xylocaine into the stretched muscle. The suppression of the response is reversible.
Experiments have been performed on unanaesthetized and paralysed cats. The tuning curves for spatial frequency of retinal, lateral geniculate and simple and complex cells of the cortex have been determined in response to sinusoidal gratings of various spatial frequencies at different levels of mean luminance. For all neurones, decreasing the mean luminance leads to a progressive loss of spatial resolution and contrast sensitivity. Retinal ganglion cells of type X show, for scotopic levels of luminance, a flattening of their spatial frequency tuning curves in the low spatial frequency range. For geniculate and cortical neurones, on the contrary, the spatial frequency characteristics at the various levels of luminance remain practically invariant in their bandwidth. On the average, complex cells still respond to mean luminances ten times lower than simple cells. The tuning curves for orientation of cortical cells maintain, to a first approximation, the same shape at the various levels of mean luminance. The results are discussed comparing the electrophysiological with psychophysical data.
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Immobilization of one eye in the adult cat following section of the oculomotor cranial nerves causes a decrease of the proportion of binocularly activated cells in the striate cortex. This change in the binocular properties of cortical cells also takes place if the animal is deprived of vision from the day on which the nerves are cut to the day of the electrophysiological recording. No similar change in the proportion of binocular cortical cells is observed in cats where both eyes have been immobilized.
Artificial strabismus in kittens decreases the proportion of binocularly driven units in area 17 of the cortex. This change in the binocular interaction of cortical cells also takes place if the kittens are deprived of vision from the day in which the strabismus is surgically produced to the day of the electrophysiological recording. Thus, altered motility of the eyes per se is sufficient to affect binocular interaction in the neurons of area 17 of the cortex.