Functional organization of the hippocampal memory system.

In humans declarative or explicit memory is supported by the hippocampus and related structures of the medial temporal lobe working in concert with the cerebral cortex. This paper reviews our progress in developing an animal model for studies of cortical-hippocampal interactions in memory processing. Our findings support the view that the cortex maintains various forms of memory representation and that hippocampal structures extend the persistence and mediate the organization of these codings. Specifically, the parahippocampal region, through direct and reciprocal interconnections with the cortex, is sufficient to support the convergence and extended persistence of cortical codings. The hippocampus itself is critical to the organization cortical representations in terms of relationships among items in memory and in the flexible memory expression that is the hallmark of declarative memory.

[1]  G. Majno,et al.  PREPARATION OF TISSUE SLICES FOR METABOLIC STUDIES: A HAND‐MICROTOME ESPECIALLY SUITABLE FOR BRAIN , 1957, Journal of neurochemistry.

[2]  H. Eichenbaum,et al.  Two functional components of the hippocampal memory system , 1994, Behavioral and Brain Sciences.

[3]  H. Eichenbaum,et al.  Conservation of hippocampal memory function in rats and humans , 1996, Nature.

[4]  H. Eichenbaum Is the rodent hippocampus just for ‘place’? , 1996, Current Opinion in Neurobiology.

[5]  M. W. Brown,et al.  Neuronal evidence that inferomedial temporal cortex is more important than hippocampus in certain processes underlying recognition memory , 1987, Brain Research.

[6]  M Mishkin,et al.  Neural substrates of visual stimulus-stimulus association in rhesus monkeys , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  H Eichenbaum,et al.  Selective damage to the hippocampal region blocks long‐term retention of a natural and nonspatial stimulus‐stimulus association , 1995, Hippocampus.

[8]  Howard Eichenbaum,et al.  Reexamination of functional subdivisions of the rodent prefrontal cortex , 1983, Experimental Neurology.

[9]  L. Squire Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. , 1992, Psychological review.

[10]  R. Rescorla "Configural" conditioning in discrete-trial bar pressing. , 1972, Journal of comparative and physiological psychology.

[11]  E. Azmitia The neuropsychology of anxiety: an enquiry into the functions of the Septo-Hippocampal system, Gray J.A.. Oxford University Press, New York (1981), pp. 523.,£27.50 , 1983 .

[12]  M. Mishkin,et al.  Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  T. Teyler,et al.  The hippocampal memory indexing theory. , 1986, Behavioral neuroscience.

[14]  D. Amaral,et al.  Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  L. Squire,et al.  Medial temporal lesions in monkeys impair memory on a variety of tasks sensitive to human amnesia. , 1985, Behavioral neuroscience.

[16]  M. Witter,et al.  Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region , 1989, Progress in Neurobiology.

[17]  G. Winocur Anterograde and retrograde amnesia in rats with dorsal hippocampal or dorsomedial thalamic lesions , 1990, Behavioural Brain Research.

[18]  R. Sutherland,et al.  Configural association theory: The role of the hippocampal formation in learning, memory, and amnesia , 1989, Psychobiology.

[19]  M. Mishkin,et al.  Visual recognition in monkeys following rhinal cortical ablations combined with either amygdalectomy or hippocampectomy , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  H. Eichenbaum,et al.  Learning‐related patterns of CA1 spike trains parallel stimulation parameters optimal for inducing hippocampal long‐term potentiation , 1991, Hippocampus.

[21]  H. Eichenbaum,et al.  Temporal relationship between sniffing and the limbic theta rhythm during odor discrimination reversal learning , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  H Eichenbaum,et al.  Critical role of the parahippocampal region for paired-associate learning in rats. , 1993, Behavioral neuroscience.

[23]  M. Mishkin Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus , 1978, Nature.

[24]  G. Schoenbaum,et al.  Information coding in the rodent prefrontal cortex. II. Ensemble activity in orbitofrontal cortex. , 1995, Journal of neurophysiology.

[25]  D. Gaffan,et al.  Recognition impaired and association intact in the memory of monkeys after transection of the fornix. , 1974, Journal of comparative and physiological psychology.

[26]  H Eichenbaum,et al.  Thalamocortical mechanisms in odor-guided behavior. I. Effects of lesions of the mediodorsal thalamic nucleus and frontal cortex on olfactory discrimination in the rat. , 1980, Brain, behavior and evolution.

[27]  G. V. Van Hoesen,et al.  Olfactory bulb projections to the parahippocampal area of the rat , 1981, The Journal of comparative neurology.

[28]  Y. Miyashita,et al.  Neural organization for the long-term memory of paired associates , 1991, Nature.

[29]  H. Eichenbaum,et al.  The hippocampus--what does it do? , 1992, Behavioral and neural biology.

[30]  L. Squire,et al.  Preserved learning and retention of pattern-analyzing skill in amnesia: dissociation of knowing how and knowing that. , 1980, Science.

[31]  W. Suzuki,et al.  Topographic organization of the reciprocal connections between the monkey entorhinal cortex and the perirhinal and parahippocampal cortices , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  Memory, amnesia, and the hippocampal system , 1994 .

[33]  Mortimer Mishkin,et al.  An analysis of short-term visual memory in the monkey. , 1975, Journal of experimental psychology. Animal behavior processes.

[34]  H. Eichenbaum,et al.  On the Binding of Associations in Memory: Clues From Studies on the Role of the Hippocampal Region in Paired-Associate Learning , 1995 .

[35]  H Eichenbaum,et al.  Information coding in the rodent prefrontal cortex. I. Single-neuron activity in orbitofrontal cortex compared with that in pyriform cortex. , 1995, Journal of neurophysiology.

[36]  Wayne A. Wickelgren,et al.  Chunking and consolidation: A theoretical synthesis of semantic networks configuring in conditioning , 1979 .

[37]  D. Amaral,et al.  Perirhinal and postrhinal cortices of the rat: A review of the neuroanatomical literature and comparison with findings from the monkey brain , 1995, Hippocampus.

[38]  J. Gray,et al.  Précis of The neuropsychology of anxiety: An enquiry into the functions of the septo-hippocampal system , 1982, Behavioral and Brain Sciences.

[39]  H Eichenbaum,et al.  Afferent connections of the perirhinal cortex in the rat , 1983, The Journal of comparative neurology.

[40]  H. Eichenbaum,et al.  Neuronal activity in the hippocampus during delayed non‐match to sample performance in rats: Evidence for hippocampal processing in recognition memory , 1992, Hippocampus.