Literature DB >> 9368937

Amnesia and neglect: beyond the Delay-Brion system and the Hebb synapse.

D Gaffan1, J Hornak.   

Abstract

Hippocampal damage in people causes impairments of episodic memory, but in rats it causes impairments of spatial learning. Experiments in macaque monkeys show that these two kinds of impairment are functionally similar to each other. After any lesion that interrupts the Delay-Brion system (hippocampus, fornix, mamillary bodies and anterior thalamus) monkeys are impaired in scene-specific memory, where an event takes place against a background that is specific to that event. Scene-specific memory in the monkey corresponds to human episodic memory, which is the memory of a unique event set in a particular scene, as opposed to scene-independent human knowledge, which is abstracted from many different scenes. However, interruption of the Delay-Brion system is not sufficient to explain all of the memory impairments that are seen in amnesic patients. To explain amnesia the specialized function of the hippocampus in scene memory needs to be considered alongside the other, qualitatively different functional specializations of other memory systems of the temporal lobe, including the perirhinal cortex and the amygdala. In all these specialized areas, however, including the hippocampus, there is no fundamental distinction between memory systems and perceptual systems. In explaining memory disorders in amnesia it is also important to consider them alongside the memory disorders of neglect patients. Neglect patients fail to represent in memory the side of the world that is contralateral to the current fixation point, in both short- and long-term memory retrieval. Neglect was produced experimentally by unilateral visual disconnection in the monkey, confirming the idea that visual memory retrieval is retinotopically organized; patients with unilateral medial temporal-lobe removals showed lateralized memory impairments for half-scenes in the visual hemifield contralateral to the removal. Thus, in scene-memory retrieval the Delay-Brion system contributes to the retrieval of visual memories into the retinotopically organized visual cortex. This scene memory interpretation of hippocampal function needs to be contrasted with the cognitive-map hypothesis. The cognitive-map model of hippocampal function shares some common assumptions with the Hebb-synapse model of association formation, and the Hebb-synapse model can be rejected on the basis of recent evidence that monkeys can form direct associations in memory between temporally discontiguous events. Our general conclusion is that the primate brain encompasses widespread and powerful memory mechanisms which will continue to be poorly understood if theory and experimentation continue to concentrate too much, as they have in the past, on the hippocampus and the Hebb synapse.

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Year:  1997        PMID: 9368937      PMCID: PMC1692054          DOI: 10.1098/rstb.1997.0135

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  34 in total

1.  Ocular exploration in the dark by patients with visual neglect.

Authors:  J Hornak
Journal:  Neuropsychologia       Date:  1992-06       Impact factor: 3.139

2.  Interaction of perirhinal cortex with the fornix-fimbria: memory for objects and "object-in-place" memory.

Authors:  D Gaffan; A Parker
Journal:  J Neurosci       Date:  1996-09-15       Impact factor: 6.167

3.  The representational capacity of the distributed encoding of information provided by populations of neurons in primate temporal visual cortex.

Authors:  E T Rolls; A Treves; M J Tovee
Journal:  Exp Brain Res       Date:  1997-03       Impact factor: 1.972

4.  Neuronal evidence that inferomedial temporal cortex is more important than hippocampus in certain processes underlying recognition memory.

Authors:  M W Brown; F A Wilson; I P Riches
Journal:  Brain Res       Date:  1987-04-14       Impact factor: 3.252

5.  Mnemonic and neuropathological effects of occluding the posterior cerebral artery in Macaca mulatta.

Authors:  J Bachevalier; M Mishkin
Journal:  Neuropsychologia       Date:  1989       Impact factor: 3.139

6.  The performance of visual tasks while segments of the inferotemporal cortex are suppressed by cold.

Authors:  J A Horel; D E Pytko-Joiner; M L Voytko; K Salsbury
Journal:  Behav Brain Res       Date:  1987-01       Impact factor: 3.332

7.  Spatial learning without NMDA receptor-dependent long-term potentiation.

Authors:  D Saucier; D P Cain
Journal:  Nature       Date:  1995-11-09       Impact factor: 49.962

8.  Recall of the goal box in latent learning and latent discrimination.

Authors:  D Gaffan; E A Gowling
Journal:  Q J Exp Psychol B       Date:  1984-02

9.  Monkeys (Macaca fascicularis) with rhinal cortex ablations succeed in object discrimination learning despite 24-hr intertrial intervals and fail at matching to sample despite double sample presentations.

Authors:  D Gaffan; E A Murray
Journal:  Behav Neurosci       Date:  1992-02       Impact factor: 1.912

10.  Hemifield-specific visual recognition memory impairments in patients with unilateral temporal lobe removals.

Authors:  J Hornak; S Oxbury; J Oxbury; S D Iversen; D Gaffan
Journal:  Neuropsychologia       Date:  1997-09       Impact factor: 3.139

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  3 in total

Review 1.  Against memory systems.

Authors:  David Gaffan
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-08-29       Impact factor: 6.237

Review 2.  Perirhinal cortex ablation impairs visual object identification.

Authors:  M J Buckley; D Gaffan
Journal:  J Neurosci       Date:  1998-03-15       Impact factor: 6.167

3.  The hippocampus is required for short-term topographical memory in humans.

Authors:  Tom Hartley; Chris M Bird; Dennis Chan; Lisa Cipolotti; Masud Husain; Faraneh Vargha-Khadem; Neil Burgess
Journal:  Hippocampus       Date:  2007       Impact factor: 3.899

  3 in total

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