Biomedical subjects

O Creutzfeldt

Publications and source records attributed to O Creutzfeldt.

14 recordsLinked to original sources

PubMed1990

Chromatic induction and brightness contrast: a relativistic color model.

It has been suggested that object colors in a colored environment are the result of combining in perception the (relative) brightness of each spectral component rather than of just mixing the spectral luminances. We tested this hypothesis with the following experiment: A pair of center-surround targets made of colored papers was illuminated with trichromatic white light. Two identical central color plates (test and match field, respectively) were surrounded by frames of different colors and thus looked different because of simultaneous color contrast. Observers were asked to match the colors by changing the illumination of the match field by means of a color-mixture projector (color match, CM). This color-matched reflectance was measured with a photometer, and its CIE coordinates were determined. We then illuminated the display with one of the three primaries that made up our trichromatic white light. The different reflectances of the different surrounds at each primary induced simultaneous brightness contrast. The brightnesses of the two central plates were therefore different. Observers were asked to change the intensity of the illumination of the match field at the respective primary so that it looked equally bright as the test field. This procedure was repeated for each primary (primary brightness match, PBM). Then the whole display except for the match field was illuminated with the trichromatic white as before, while the latter was illuminated with a trichromatic mixture consisting of the primaries at the intensities as set in the PBM experiment, and the CIE values were determined with the photometer. The CIE values of the match field after the CM and PBM procedures were nearly identical. This indicates that composite colors are composed in perception by combining the scaled (or relative) brightness of each spectral component and that this brightness scaling is largely restricted to interactions in the same spectral region. The results are compared with those of other models concerned with contrast colors as well as with neurophysiological data. Some limitations are mentioned.

Adult↗

PubMed1989

Neuronal activity in the human lateral temporal lobe. I. Responses to speech.

Single and multiple unit neuronal activity was recorded from the cortex of the lateral temporal lobe in conscious humans during open brain surgery for the treatment of epilepsy. Recordings were obtained from the right and left superior, middle and inferior temporal gyrus of 34 patients (41 recording sites). Recordings were restricted to regions to be resected during subsequent surgery. This excluded recordings from language areas proper. Neuronal responses to words and sentences presented over a loudspeaker and during free conversation were recorded. No significant differences between the right and left hemisphere were obvious. All neurons in the superior temporal gyrus responded to various aspects of spoken language with temporally well defined activation/inhibition patterns, but not or only little to non-linguistic noises or tones. Excitatory responses were typically short or prolonged (up to several hundred ms) bursts of discharges at rates above 20/sec, reaching peak rates of 50-100/s. Such responses could be specifically related to certain combinations of consonants suggesting a function in categorization, they could depend on word length, could differentiate between polysyllabic and compound words of the same length or could be unspecifically related to language as such. No formant specific responses were found, but the prolonged excitations across syllables suggest that consonant/vowel combinations may play a role for some activation patterns. Responses of some neurons (or neuronal populations) depended on the attention paid to the words and sentences, or the task connected with them (repeat words, speech addressed to the patient demanding something). Neurons in the middle and inferior temporal gyrus were only little affected by listening to single words or sentences, but some were unspecifically activated by words or while listening to sentences. Excitatory responses varied within a limited range of discharge rates usually below 5-10/s. Phonetic distortion of spoken language could reduce responses in superior temporal gyrus neurons, but also the slight changes in discharge rate of middle temporal neurons could be absent during distorted and uncomprehensible speech sounds. We conclude that superior temporal gyrus neuron responses reflect some general phonetic but not semantic aspects of spoken language. Middle and inferior temporal gyrus neurons do not signal phonetic aspects of language, but may be involved in understanding language under certain conditions.

Epilepsy↗

PubMed1989

Neuronal activity in the human lateral temporal lobe. II. Responses to the subjects own voice.

We have recorded neuronal responses in the lateral temporal lobe of man to overt speech during open brain surgery for epilepsy. Tests included overt naming of objects and reading words or short sentences shown on a projector screen, repetition of tape recorded words or sentences presented over a loudspeaker, and free conversation. Neuronal activity in the dominant and non-dominant temporal lobe were about equally affected by overt speech. As during listening to language (see Creutzfeldt et al. 1989), responses differed between recordings from sites in the superior and the middle or inferior temporal gyrus. In the superior temporal gyrus all neurons responded clearly and each in a characteristic manner. Activation could be related to phonemic aspects, to segmentation or to the length of spoken words or sentences. However, neurons were mostly differently affected by listening to words and language as compared to overt speaking. In neuronal populations recorded simultaneously with one or two microelectrodes, some neurons responded predominantly to one or the other type of speech. Excitatory responses during overt speaking were always auditory. In the middle temporal gyrus more neurons (about 2/3) responded to overt speaking than to listening alone. Activations elicited during overt speech were seen in about 1/3 of our sample, but they were more sluggish than those recorded in the superior gyrus. A prominent feature was suppression of on-going activity, which we found in about 1/3 of middle and in some superior temporal gyrus neurons. This suppression could precede vocalization by up to a few hundred ms, and could outlast it by up to 1 s. Evoked ECoG-potentials to words heard or spoken were different, and those to overt speech were more widespread.

Emotions↗

PubMed1989

Neuronal activity in the human lateral temporal lobe. III. Activity changes during music.

During open brain surgery under local anesthesia for the treatment of medically intractable temporal lobe epilepsy we have recorded neuronal activity from the lateral temporal lobe with microelectrodes while the patients listened to short pieces of music. Three groups of music were tested: A) Simple familiar or unknown classical tunes at a simple rhythm and harmony, played on piano; B) Orchestrated folk music; C) Drumming without a tune. All types of music lead to changes of neuronal discharge rate. Musical pieces of type A produced a decrease in 48% of the recordings, an increase in about 17% and had no effect in 30%. A similar distribution of effects was found during type B-music (48%, 22%, 30%, respectively). During type C, only 26% showed a decrease and 74% an increase. When music was turned off, usually the reverse change from that caused by music was seen. In addition to changes of discharge rate, a slight entrainment of activity by single, regularly appearing notes (rhythm) was seen in some neurons. A few neurons showed a change of activity related to musical phrases (activation towards the end of a 4-bar 4/4 phrase). In contrast to the effects of verbal stimuli and overt speech, the effects of music on discharge rates did not show obvious topographical differences between superior, middle and inferior temporal gyrus. They also were bilateral with no significant right-left differences.

Acoustic Stimulation↗

PubMed1988

Neuronal activity in human lateral temporal cortex related to short-term verbal memory, naming and reading.

Extracellular microelectrode recordings were obtained from lateral temporal cortex that was subsequently resected in patients undergoing craniotomies under local anaesthesia for treatment of medically intractable epilepsy. During these recordings patients performed visually presented measures of overt and silent naming and word reading, short-term verbal memory and a control task requiring matching of angles. These measures were designed so that the same visual stimuli elicited language, short-term memory or spatial responses. Statistically significant changes within and between these various measures were identified. Technically satisfactory recordings were obtained from 17 populations reflecting activity predominantly from 1 neuron, in 13 patients. Two populations demonstrated no significant changes in any measured functions. Only 1 population showed changes suggesting a relation to visual perception. Four populations in or adjacent to the superior temporal gyrus altered activity with overt speech. Four other populations in the anterior temporal lobe altered activity during silent, but not overt speech. Some relation to language or memory was established for 13 of the 17 populations: 1 altered activity during reading alone, 6 during memory alone, and 6 to both. Most of the recording sites showing these language and memory changes were not essential for those functions based on surface electrical stimulation mapping. Thus the area of temporal lobe that participates in language and memory, as indicated by changes in neuronal activity, is substantially larger than the areas essential for those functions as determined by stimulation mapping. Within that participatory area, changes related to language were most often an increase in activity sustained throughout the task, a pattern suggestive of mechanisms of selective attention. Changes related to memory most often included a sustained increase in activity at the time of entry of information into memory, and again at retrieval, with decreased activity during the time the memory was stored. A few neuronal populations demonstrated relative inhibition of activity during the memory task, compared with control measures.

Electric Stimulation↗

PubMed1987

Darkness induction, retinex and cooperative mechanisms in vision.

We have investigated the darkness induction of surround fields of various composition on a centrally located test field. Darkness induction can be described as a linear subtraction of the luminance of the induction region from the test field luminance, weighted for the size, the length of immediate contact and the distance of the induction field from the test field. Furthermore, closer induction fields exert a shunting effect on the induction effect of fields which are more distally located on the same radius, and neighbouring fields mutually interact. A model is discussed which takes into account these variables. It is compared with older models as well as with the Retinex-model as formulated by Land (1983). Our data and model are closer to the model of Jameson and Hurvich (1964). Neurophysiological correlates and mechanisms are discussed.

Adult↗

PubMed1986

Colour and brightness signals of parvocellular lateral geniculate neurons.

We recorded from single neurons in the parvocellular layers of the lateral geniculate body of anesthetized monkeys. Spectral response curves of parvocellular neurons depended on the luminance ratio between the chromatic stimuli and achromatic background. From response/intensity curves, we determined the relative luminance between a coloured and an achromatic (white) light at which a given cell became non-responsive (critical luminance ratio, CLR). The spectral dependence of the CLRs of narrow (N) and wide band (W) cells with opponent receptor input showed characteristic differences. The activity of W-cells increased with luminance increase of a white light and of a coloured light in the specific spectral region of the cell (yellow-red for the long wave length sensitive WL-, and yellow-green-blue for the short wave length sensitive WS-cells), while N-cells were activated by their specific spectral light (blue for NS-cells, red for NL-cells) and by a luminance decrease of achromatic white. N-cells discriminate best between their characteristic colour and white at luminance ratios below their respective CLR, while W-cells distinguish best between a light of their characteristic colour and white at chromatic/achromatic luminance ratios above their respective CLR. Yellow sensitive W-cells with a narrow spectral sensitivity peaking around 570 nm and with only a small or no response to white light, could enable distinction between white and yellow of similar luminance. The findings are consistent with the opponency model of spectrally sensitive cells in the LGB. We discuss their implications for colour coding by parvocellular cells. N- and W-cells appear to behave complementary with respect to luminance information (N-cells may be compared to the cat's off-cells, W-cells to on-cells). S- and L-cells are complementary with respect to colour. The yellow sensitive WM-cells are critical for the discrimination of yellow and white, while cells with excitatory cone input from blue and red cones (W-SL-cells) may aid the perception of purple. The fact that, at different relative luminance ratios between a chromatic stimulus and a white background, the whole family of parvocellular cells is involved differently in coding for colour, may explain the different appearance of colours against a white background at different luminance ratios and the perception of induced colours.

Animals↗

PubMed1979