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Computational analysis of the role of the hippocampus in memory
- Hippocampus
, 1994
"... The authors draw together the results of a series of detailed computational studies and show how they are contributing to the development of a theory of hippocampal function. A new part of the theory introduced here is a quantitative analysis of how backprojections from the hippocampus to the neocor ..."
Abstract
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Cited by 95 (10 self)
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The authors draw together the results of a series of detailed computational studies and show how they are contributing to the development of a theory of hippocampal function. A new part of the theory introduced here is a quantitative analysis of how backprojections from the hippocampus to the neocortex could lead to the recall of recent memories. The theory is then compared with other theories of hippocampal function. First, what is computed by the hippocampus is considered. The hypothesis the authors advocate, on the basis of the effects of damage to the hippocampus and neuronal activity recorded in it, is that it is involved in the formation of new memories by acting as an intermediate-term buffer store for information about episodes, particularly for spatial, but probably also for some nonspatial, information. The authors analyze how the hippocampus could perform this function, by producing a computational theory of how it operates, based on neuroanatomical and neurophysiological information about the different neuronal systems con-tained within the hippocampus. Key hypotheses are that the CA3 pyramidal cells operate as a single autoassociation network to store new episodic information as it arrives via a number of specialized preprocessing stages from many association areas of the cerebral cortex, and that the dentate
The Orbitofrontal Cortex and Reward
, 2000
"... this paper. The cortex on the orbital surface of the frontal lobe includes area 13 caudally and area 14 medially, and the cortex on the inferior convexity includes area 12 caudally and area 11 anteriorly (Fig. 1) (Carmichael and Price, 1994; Petrides and Pandya, 1994; Price et al., 1996). This br ..."
Abstract
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Cited by 36 (4 self)
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this paper. The cortex on the orbital surface of the frontal lobe includes area 13 caudally and area 14 medially, and the cortex on the inferior convexity includes area 12 caudally and area 11 anteriorly (Fig. 1) (Carmichael and Price, 1994; Petrides and Pandya, 1994; Price et al., 1996). This brain region is well developed in primates, including humans, but poorly developed in rodents, with homologies to areas found in primates uncertain, so that care must be used in interpretation of the term `orbitofrontal ' when applied to rodents (Uylings and van Eden, 1990). To understand the function of this brain region in humans, the majority of the studies described were therefore performed with macaques or with humans
Right-Hemisphere Dominance for the Processing of Sound-source Lateralization
, 2000
"... Cortical processing of change in direction of a perceived sound source was investigated in 12 human subjects using whole-head magnetoencephalography. The German word “da ” was presented either with or without 0.7 msec interaural time delays to create the impression of right- or left-lateralized or m ..."
Abstract
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Cited by 5 (1 self)
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Cortical processing of change in direction of a perceived sound source was investigated in 12 human subjects using whole-head magnetoencephalography. The German word “da ” was presented either with or without 0.7 msec interaural time delays to create the impression of right- or left-lateralized or midline sources, respectively. Midline stimuli served as standards, and lateralized stimuli served as deviants in a mismatch paradigm. Two symmetrically linked dipoles fitted to the mismatch fields showed stronger moments in the hemisphere contralateral to the side of the deviant. The right dipole displayed equal latencies to both left and right deviants, whereas left dipole latencies were longer for ipsilateral than contralateral deviants. Frequency analysis between 20–70 Hz and statistical probability mapping revealed increased induced gamma-band activity at 53 � 2.5 Hz to both types of deviants. Right deviants elicited spectral amplitude
FEATURE ARTICLE Human Functional Neuroimaging of Brain Changes Associated with Practice
, 2005
"... The discovery that experience-driven changes in the human brain can occur from a neural to a cortical level throughout the lifespan has stimulated a proliferation of research into how neural function changes in response to experience, enabled by neuroimaging methods such as positron emission tomogra ..."
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The discovery that experience-driven changes in the human brain can occur from a neural to a cortical level throughout the lifespan has stimulated a proliferation of research into how neural function changes in response to experience, enabled by neuroimaging methods such as positron emission tomography and functional magnetic resonance imaging. Studies attempt to characterize these changes by examining how practice on a task affects the functional anatomy underlying performance. Results are incongruous, including patterns of increases, decreases and functional reorganization of regional activations. Following an extensive review of the practice-effects literature, we distinguish a number of factors affecting the pattern of practice effects observed, including the effects of task domain, changes at the level of behavioural and cognitive processes, the time-window of imaging and practice, and of a number of other influences and miscellaneous confounding factors. We make a novel distinction between patterns of reorganization and redistribution as effects of task practice on brain activation, and emphasize the need for careful attention to practicerelated changes occurring on the behavioural, cognitive and neural levels of analysis. Finally, we suggest that functional and effective connectivity analyses may make important contributions to our understanding of changes in functional anatomy occurring as a result of practice on tasks.

