Biomedical subjects

P E Roland

Publications and source records attributed to P E Roland.

At least 19 recordsLinked to original sources

PubMed1996

Cortical representation of self-paced finger movement.

We compared the cortical fields activated by simple, self-paced index-finger flexions with those activated during visually triggered movement and rest using PET. Of 12 fields detected during self-paced movement compared to rest, three were located in the classically defined motor areas: primary motor area (M1), premotor cortex (PM) and supplementary motor area (SMA). The latter extended into the cingulate motor area (CMA). Four corresponding clusters were also found when triggered movement was subtracted from self-paced movement. The change in regional cerebral blood flow (rCBF) was greater in SMA than in PM during self-paced movement compared with either control. We conclude that repetitive, self-paced index-finger flexions can activate SMA, PM and CMA, and that this movement activates SMA more strongly than PM.

Adult↗

PubMed1996

Activation by attention of the human reticular formation and thalamic intralaminar nuclei.

It has been known for over 45 years that electrical stimulation of the midbrain reticular formation and of the thalamic intralaminar nuclei of the brain alerts animals. However, lesions of these sectors fail to impair arousal and vigilance in some cases, making the role of the ascending activating reticular system controversial. Here, a positron emission tomographic study showed activation of the midbrain reticular formation and of thalamic intralaminar nuclei when human participants went from a relaxed awake state to an attention-demanding reaction-time task. These results confirm the role of these areas of the brain and brainstem in arousal and vigilance.

Adult↗

PubMed1995

Somatosensory activations of the parietal operculum of man. A PET study.

We tested the hypothesis that somatosensory discrimination of roughness (microgeometry) but not of shape (macrogeometry) would activate the parietal operculum (PO) in man. It was also investigated whether a simple square pulse indentation of the skin on the index finger would activate the PO. Regional cerebral blood flow was measured with [15O]butanol and positron emission tomography in a total of 20 normal volunteers. Ten subjects used their right hand to discriminate objects that differed in roughness and similar smooth objects that differed in length. Ten other subjects pressed a button when they felt a square pulse indentation of the skin on their right index finger in a somatosensory reaction time task. Discrimination of roughness activated one field in the PO contralaterally and two fields ipsilaterally to the stimulated hand. The discrimination of length activated one field in the PO located ipsilaterally to the stimulated hand. The somatosensory reaction time task also activated one contralateral and two ipsilateral fields in the PO, and these fields partially overlapped the activated fields in the roughness discrimination task. Based on the extension of these fields and their overlaps we conclude that there exist at least one part of the contralateral PO and at least two parts of the ipsilateral PO that can be activated by somatosensory stimulation of the right hand. We argue further that the contralateral activated part contains a region than can be activated by roughness.

Adult↗

PubMed1995

Positron-emission tomography studies of cross-modality inhibition in selective attentional tasks: closing the "mind's eye".

It is a familiar experience that we tend to close our eyes or divert our gaze when concentrating attention on cognitively demanding tasks. We report on the brain activity correlates of directing attention away from potentially competing visual processing and toward processing in another sensory modality. Results are reported from a series of positron-emission tomography studies of the human brain engaged in somatosensory tasks, in both "eyes open" and "eyes closed" conditions. During these tasks, there was a significant decrease in the regional cerebral blood flow in the visual cortex, which occurred irrespective of whether subjects had to close their eyes or were instructed to keep their eyes open. These task-related deactivations of the association areas belonging to the nonrelevant sensory modality were interpreted as being due to decreased metabolic activity. Previous research has clearly demonstrated selective activation of cortical regions involved in attention-demanding modality-specific tasks; however, the other side of this story appears to be one of selective deactivation of unattended areas.

Brain↗

PubMed1995

Mapping of human and macaque sensorimotor areas by integrating architectonic, transmitter receptor, MRI and PET data.

The human and macaque sensorimotor cortex was subdivided into numerous areas by a correlative analysis based on cytoarchitectonics, myeloarchitecture and the distribution of transmitter receptors. Receptor densities and laminar distribution patterns differ not only between motor and somatosensory regions, but also between different areas within these regions of the cortex. Changes in receptor distribution often match architectonically defined borders. Receptor findings provide new criteria for a more detailed mapping in the human brain which cannot be achieved by cytoarchitectonic analysis alone. Morphological data on these areas were integrated with functional data from positron emission tomography (PET) on the basis of a recently developed computerised brain atlas. The central sulcus marks the border between (1) the agranular motor cortex with a generally low density of glutamatergic, muscarinic, GABAergic and serotoninergic receptors, and (2) the granular somatosensory cortex with higher densities of these receptors. Rostral to the primary motor cortex, 2 isocortical areas are found on the mesial cortex which probably represent the functionally defined supplementary motor areas (SMA) SMA-proper (caudally) and pre-SMA (rostrally). Below SMA-proper the areas 24d (macaque) and the caudal cingulate motor area cmc (human) are located in the cingulate sulcus. Both regions correspond to the 'posterior cingulate motor areas' of recent PET studies and to the posterior part of the agranular cingulate cortex of architectonic studies. Below pre-SMA the area 24c (macaque) and the rostral cingulate motor area cmr (human) are located in the cingulate sulcus; they correspond to the 'anterior cingulate motor areas' of recent PET observations and to the anterior part of the agranular cingulate cortex of architectonic studies. Homologous sensorimotor areas can be defined in both species on the basis of common architectonic features.

Animals↗

PubMed1994

The human entorhinal cortex participates in associative memory.

Animal studies have shown that lesions of the parahippocampal cortex impair learning of visual stimulus-stimulus associations. We tested the hypothesis that recall of paired associates, in contrast to recall of non-associated items, activates the parahippocampal cortex in humans. Ten volunteers had their regional cerebral blood flow measured with positron emission tomography during non-associative recall, and during two conditions with associative recall of visual stimuli. Compared with non-associative recall, associative recall specifically increased the blood flow in a field located in the entorhinal cortex, extending into the presubiculum. Our results demonstrate functional differences between the human hippocampal and parahippocampal cortex, and show that the entorhinal cortex is engaged in associative memory.

Association Learning↗

PubMed1994

Processing and analysis of form, colour and binocular disparity in the human brain: functional anatomy by positron emission tomography.

With the purpose of mapping those anatomical structures participating in the processing and analysis of form, colour and disparity information, we have measured, with positron emission tomography and [15O]butanol, regional cerebral blood flow (rCBF) as an indicator of regional cerebral metabolic activity in 13 right-handed male volunteers during visual discrimination of colour, form and disparity information. The brain images were anatomically standardized using a computerized brain atlas and statistically significant changes were localized by cluster analysis. The changes in rCBF between specific activation and reference states were measured and the volumes of changes were determined, as were the loci and volumes of areas commonly activated by two or three different tasks. Each of the tasks activated over a dozen distinct and separate fields in the cortex--in the occipital, parietal, temporal and frontal lobes as well as the cerebellum. A number of overlapping fields were commonly activated in two tasks (four in the form and colour tasks, five in the form and disparity tasks, and eleven in the colour and disparity tasks), and two field overlaps were present in all three tasks (in the right superior frontal and left lingual gyri). These findings indicate that, in a visual discrimination task, the processing and analysis of single visual submodalities take place in a number of cortical fields in the human brain. As the same visual submodality is processed and analysed by numerous fields and the same field may participate in the processing of different submodalities, a divergence-convergence pattern of information processing is present in the human brain. This observation supports a hypothesis based on earlier studies in primates, namely that information processing in the visual system requires the concerted activation of a relatively large number of fields of functional networks in the brain.

Adult↗

PubMed1994

Visual form discrimination from luminance or disparity cues: functional anatomy by PET.

With the purpose of elucidating the functional fields involved in the discrimination of visual form based either on luminance or binocular disparity cues, we used PET to measure changes in regional cerebral blood flow (rCBF) in ten volunteers while they performed visual discrimination tasks. The averaged standardized subtraction images (delta rCBF) were analysed for statistically significant changes between the form tasks and their reference tasks. Twenty cortical fields in the visual association areas and the prefrontal cortex were engaged by the discrimination of visual form based upon disparity cues, whereas only four fields showed increased activity during the discrimination of visual form created by luminance cues. The only functional field activated in both conditions was in the left fusiform gyrus. The present findings extend our earlier observations, namely that disparate functional networks of activated fields in the human brain can perform the discrimination of visual form perceptually defined by different visual cues.

Adult↗

PubMed1994

Activity in the human primary motor cortex related to ipsilateral hand movements.

In two studies with positron emission tomography (PET), we found that somatosensory discrimination of length activated the ipsilateral MI, but somatosensory discrimination of shape did not. This occurred even though both tasks required the exclusive use of distal finger and hand movements which were also very similar in both tasks. The activation of the ipsilateral MI was correlated with activations of the premotor cortex in the other hemisphere, the prefrontal cortex and the posterior cingulate cortex, indicating that these areas together with the ipsilateral MI constitute a task-related active network.

Discrimination Learning↗

PubMed1994

Obstacles on the road towards a neuroscientific theory of mind.

In the efforts to establish neuroscientific theories of the mind, one should distinguish between conceptual and scientific obstacles. The conceptual obstacles comprise, for example, various dualist-materialist philosophical positions, emergentism, failure to distinguish between models and non-models, lack of ontological commitment, and the constraints of language. The scientific obstacles comprise, for example, the lack of methods to describe the behaviour of neuron networks and their properties, the difficulties of establishing transition rules between micro-networks and macro-networks, the difficulties in working with non-Pavlovian paradigms and imposing information processing constraints and informational requirements on brain processes.

Animals↗

PubMed1994

Visual form discrimination from color or motion cues: functional anatomy by positron emission tomography.

To explore the extent to which various cortical functional pathways are involved in processing and analyzing different types of information that yield the same perceptual entity, we mapped anatomical structures in the human brain participating in the discrimination of visual forms mediated either by motion or color cues. Changes in regional cerebral blood flow were measured in 10 young male volunteers with positron emission tomography and with [15O]butanol. During the measurements, the subjects performed four visual discrimination tasks (form-from-motion, motion alone, form-from-color, and color alone discrimination). The individual regional cerebral blood flow images were standardized in shape and size with the help of a computerized brain atlas. Subtraction images were determined and averaged across data from all subjects. The resulting images were analyzed for statistically significant changes between specific and reference tasks. The discrimination of form by means of motion cues activated functional fields bilaterally in the inferior and lateral occipital gyri, in the lingual, anterior cingulate, middle frontal and orbitofrontal gyri, and in the left fusiform and right inferior temporal gyri. Form discrimination by color cues resulted in activation bilaterally in the inferior temporal, lateral occipital, and orbitofrontal gyri, the left precuneus and intraparietal sulcus, and the right precentral gyrus. The regions engaged in the two kinds of form discrimination did not overlap, demonstrating that differences in visual forms mediated by color or motion cues are processed and analyzed by disparate networks of functional fields in human cerebral cortex.

Adult↗

PubMed1994

Binocular disparity discrimination in human cerebral cortex: functional anatomy by positron emission tomography.

Neurobiological studies in higher primates indicate that the processing of stereoscopic information takes place at early levels in the visual cortex. To map the anatomical structures in the human brain participating in pure stereopsis based upon binocular disparity, we measured with positron emission tomography the changes in regional cerebral blood flow as an indicator of metabolic activity in 10 healthy young men during visual discrimination of binocular disparity. The data demonstrate that the discrimination of pure stereo-optic disparity information takes place in the polar striate cortex and the neighboring peri-striate cortices, as well as in the parietal lobe, the prefrontal cortex, and the cerebellum. The discrimination of stereoscopic depth is dependent on a network composed of multiple functional fields localized in occipital- and parietal-lobe visual areas as well as in the dorsolateral and mesial prefrontal cortex. The findings support the importance of coactivated occipitoparietal visual areas in the processing and analysis of binocular depth information in humans.

Adult↗

PubMed1994

A PET study of somatosensory discrimination in man. microgeometry versus macrogeometry.

The regional cerebral blood flow (rCBF) was measured with 15O-butanol and positron emission tomography (PET) in 10 healthy subjects in order to compare cerebral activation involved in the somatosensory discrimination of microgeometric features with cerebral activation associated with the discrimination of macrogeometric features. Subjects performed two-alternative forced choice (2-AFC) discriminations of pairs of stimuli from a series of quantified standardized stimuli that differed in roughness (microgeometry), and a separate 2-AFC task of smooth tactile stimuli that differed in length (macrogeometry). Results are presented from three conditions: (1) a roughness discrimination task; (2) a length discrimination task; and (3) a control trial in which subjects were required to reproduce similar exploratory finger movements only, but without a specific stimulus to feel. Mean subtraction images were computed using the computerized adjustable brain atlas of Greitz et al. (1991, J. Comput. Assisted Tomogr., 15, 26-38) and areas of significant blood flow change were identified. Both the roughness and the length discrimination tasks activated overlapping cortical fields contralaterally in the anterior and posterior lip of the postcentral sulcus. However, in the length discrimination, activation of the posterior lip of the postcentral sulcus extended deeper into the sulcus and there was also a separate additional area of activation in the anterior part of the precentral gyrus. Furthermore, the length discrimination task activated fields in the overt part of the supramarginal gyrus bilaterally as well as fields in the angular gyrus bilaterally. Thus roughness discrimination uses only a subset of the cortical regions that are needed for the recovery of length information, which requires more extensive somatosensory processing. This finding may be partly explained in that length perception needs both edge detection of the stimuli used, as well as integrated information of surface length and velocity, which is not necessary for roughness perception. Specific differences in the acquisition of necessary tactile information between the two discrimination tasks was reflected in different sampling strategies.

Adult↗

PubMed1994

Visual imagery and visual representation.

Among many controversies in visual neuroscience is whether visual imagery of objects, scenes and living beings is based upon contributions of the early visual areas or depends on hierarchical higher visual areas only, and whether the cortical areas subserving visual imagery are identical to those underlying visual perception. These questions are important for furthering our understanding of vision, since areas active in visual imagery might tell us how the visual cortex represents objects, scenes and living beings. Here, P.E. Roland and B. Gulyás present their hypothesis, based on experimental evidence in man and primates, that the visual areas subserving visual imagery are parieto-occipital and temporo-occipital visual association areas, and that these areas form only a subset of the visual areas engaged in perception. This hypothesis is consistent with the view that objects, scenes and living beings are represented, stored and re-evoked outside the domain of the primary visual cortex and its immediate neighbours.

Animals↗

PubMed1994

Brain atlases--a new research tool.

Conventional brain atlases are collections of micrographs or schematic drawings of brain sections from one or a few brains in which anatomical structures are identified, for example, nuclei, cortical areas and fibre tracts. Conventional brain maps have now been replaced with modern computer-based brain atlases. The structures in computerized atlases are deformable so as to fit the sizes and shapes of individual brains, and transform three-dimensional reconstructions or images of brains into a standard brain format. In order to make generalizations about localization of function and structure at both the macroscopical and microscopical level computerized brain atlases are needed. Computerized brain atlases are also used to compensate for the shrinkage and distortions during sectioning and embedding of post-mortem brains, to study structural-functional relationships in the human brain at both the macroscopical and microscopical level, and variations in gross morphology and microstructure of the human brain, and for establishing a three-dimensional human-brain database for all of the above and also for topographically defined data from the literature.

Animals↗

PubMed1994

Fields in human motor areas involved in preparation for reaching, actual reaching, and visuomotor learning: a positron emission tomography study.

The purpose of this study was to examine the functional organization of motor cortices in the human brain involved in reaching and visuomotor learning. All subjects were asked to learn the positions of seven circular targets projected on a screen. Each time the targets were turned off, they were required to close their eyes and keep them closed, and, after a delay, to point to the center of the targets in a prescribed order using their right hand. The regional cerebral blood flow (rCBF) was measured with 15O-butanol and positron emission tomography in 20 subjects during a rest state, an initial learning stage, and a later learning stage. Ten subjects constituted the reaching group in which rCBF was measured during actual reaching; the 10 other subjects constituted the preparation group in which rCBF was measured in the delay period between target exposure and actual reaching. Individual subtraction images (each stage minus rest) were calculated and transformed into a standard size and shape brain image by the adjustable computerized brain atlas and averaged, after which significant changes of rCBF were identified. In all reaching and preparation for reaching phases, cortical fields were activated in the left primary motor area (M1) and the left premotor area (PMA). Within M1, fields active in the delay phases were adjacent to the fields active only during actual reaching movements. During the course of learning, additional fields of activity appeared in both M1 and PMA. The results indicate that three types of fields occur in M1 and PMA: (1) fields directly engaged in the efferent control of peripheral muscle contraction, (2) fields engaged in preparatory activity for reaching, and (3) fields appearing after learning of the task has taken place.

Adult↗

PubMed1993

Partition of the human cerebellum in sensory-motor activities, learning and cognition.

The circuitry of the cerebellum is quite well understood. The computation takes place in the cerebellar cortex, which functions in synchronized strips to provide excellent timing signals to the cerebral cortex and the spinal cord. The cerebellar cortex is also the site where error signals from other parts of the central nervous system are incorporated. For voluntary limb movements the cerebellar cortex is important for the timing of the innervation of the agonist and antagonist anterior horn neurons. It is also important for the temporal order of and precision in the execution of motor programs. As will be apparent, the cerebellum is not only a computer taking care of motor programs.

Cerebellum↗

PubMed1992

Vibratory stimulation increases and decreases the regional cerebral blood flow and oxidative metabolism: a positron emission tomography (PET) study.

The aim of this study was to examine the hypothesis, if the activation of some cerebral structures due to physiological stimulation is accompanied by deactivations of other structures elsewhere in the brain. A vibratory stimulus was applied to the right hand palm of healthy volunteers and the regional cerebral blood flow (rCBF) and regional cerebral oxygen metabolism (rCMRO2) were measured with positron emission tomography (PET). Regional analysis and voxel-by-voxel plots indicated that the stimulation induced increases and decreases of the rCBF were coupled to increases and decreases of the rCMRO2. The increases were localized in the left primary somatosensory area (SI), the left secondary somatosensory area (SII), the left retroinsular field (RI), the left anterior parietal cortex, the left primary motor area (MI), and the left supplementary motor area (SMA). The decreases occurred bilaterally in the superior parietal cortex, in paralimbic association areas, and the left globus pallidus. The increases and decreases of the rCBF and rCMRO2 were balanced in such a way that the mean global CBF and CMRO2 did not change compared with rest. We conclude that the decreases of the cerebral oxidative metabolism indicated regional depressions of synaptic activity.

Adult↗