Role of the hippocampal system in associative learning beyond the spatial domain.

Expert opinion remains divided on the issue of whether the hippocampal system functions exclusively in spatial information processing, e.g. in navigation or in understanding spatial relations, or whether it plays a more general role in higher brain function. Previous work on monkeys and rats has tended to support the former view, whereas observations in the clinic point to the latter, including functions as diverse as declarative knowledge, episodic memory, word learning, and understanding relations among objects. One influential theory posits a general role for the hippocampal system in associative learning, with emphasis on associations learned rapidly and recently. The results presented here are consistent with this theory, along with previous clinical and theoretical studies indicating that the hippocampal system is necessary for associative learning even if no component of the association relies on spatial information. In the study reported here, rhesus monkeys learned a series of conditional stimulus-response associations involving complex visual stimuli presented on a video monitor. Each stimulus instructed one of three responses: tapping the stimulus with the hand, steady hand contact with the stimulus for a brief period of time, or steady contact for a longer time. Fornix transection impaired the learning of these associations, even though both the stimuli and the responses were nonspatially differentiated, and this deficit persisted for at least 2 years. This finding indicates that the hippocampal system plays an important role in associative learning regardless of the relevance of spatial information to any aspect of the association. Fornix-transected monkeys were impaired in learning new stimulus-response associations even when the stimuli were highly familiar. Thus, the deficit was one of associating each stimulus with a response, as opposed to problems in distinguishing the stimuli from each other. In contrast to these effects, fornix transection did not impair performance when familiar stimuli instructed a response according to an already-learned association, which shows that the deficit was one of learning new associations rather than one of retention or retrieval of previously learned ones. Taken together, these results show that fornix transection causes a long-lasting impairment in associative learning outside of the spatial domain, in a manner consistent with theories of hippocampal-system function that stress a general role in the rapid acquisition of associative knowledge.

[1]  R. Morris,et al.  Place navigation impaired in rats with hippocampal lesions , 1982, Nature.

[2]  D. Crews,et al.  Effects of medial and dorsal cortex lesions on spatial memory in lizards , 2001, Behavioural Brain Research.

[3]  R. Dolan,et al.  Dissociating prefrontal and hippocampal function in episodic memory encoding , 1997, Nature.

[4]  David Gaffan,et al.  Inferotemporal-frontal disconnection and fornix transection in visuomotor conditional learning by monkeys , 1988, Behavioural Brain Research.

[5]  R. Ridley,et al.  Restoration of learning ability in fornix-transected monkeys after fetal basal forebrain but not fetal hippocampal tissue transplantation , 1992, Neuroscience.

[6]  R. Saunders,et al.  The relationships between temporal lobe and diencephalic structures implicated in anterograde amnesia. , 1997, Memory.

[7]  M. Petrides,et al.  Conditional associative learning and the hippocampal system , 1998, Hippocampus.

[8]  M. Mishkin,et al.  Hippocampectomized monkeys can remember one place but not two , 1993, Neuropsychologia.

[9]  S P Wise,et al.  The role of ventral and orbital prefrontal cortex in conditional visuomotor learning and strategy use in rhesus monkeys (Macaca mulatta). , 2001, Behavioral neuroscience.

[10]  J. Aggleton,et al.  Differential cognitive effects of colloid cysts in the third ventricle that spare or compromise the fornix. , 2000, Brain : a journal of neurology.

[11]  F. Craik,et al.  Novelty and familiarity activations in PET studies of memory encoding and retrieval. , 1996, Cerebral cortex.

[12]  L. Squire "Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans": Correction. , 1992 .

[13]  John F. Disterhoft,et al.  Hippocampus-dependent learning facilitated by a monoclonal antibody or D-cycloserine , 1992, Nature.

[14]  Anthony A Wright,et al.  Object and spatial relational memory in adult rhesus monkeys is impaired by neonatal lesions of the hippocampal formation but not the amygdaloid complex , 2002, Hippocampus.

[15]  D. Gaffan,et al.  What is a memory system? Horel's critique revisited , 2001, Behavioural Brain Research.

[16]  R. Clark,et al.  Classical conditioning and brain systems: the role of awareness. , 1998, Science.

[17]  Karl J. Friston,et al.  Segregating the functions of human hippocampus. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J F Disterhoft,et al.  Hippocampal encoding of non‐spatial trace conditioning , 1999, Hippocampus.

[19]  J. Aggleton,et al.  Integrating systems for event memory: testing the contribution of the fornix , 2002 .

[20]  E. Tulving,et al.  Hippocampal PET activations of memory encoding and retrieval: The HIPER model , 1998, Hippocampus.

[21]  M. Moss,et al.  The Monkey and the Sea Horse , 1986 .

[22]  J. O’Keefe Place units in the hippocampus of the freely moving rat , 1976, Experimental Neurology.

[23]  T. Bussey,et al.  Fornix Lesions Can Facilitate Acquisition of the Transverse Patterning Task: A Challenge for “Configural” Theories of Hippocampal Function , 1998, The Journal of Neuroscience.

[24]  R. Ridley,et al.  Crossed unilateral lesions of temporal lobe structures and cholinergic cell bodies impair visual conditional and object discrimination learning in monkeys , 2002, The European journal of neuroscience.

[25]  E. Tulving Episodic memory and common sense: how far apart? , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[26]  T. Bussey,et al.  Distinct patterns of behavioural impairments resulting from fornix transection or neurotoxic lesions of the perirhinal and postrhinal cortices in the rat , 2000, Behavioural Brain Research.

[27]  M. Mishkin,et al.  Object Recognition and Location Memory in Monkeys with Excitotoxic Lesions of the Amygdala and Hippocampus , 1998, The Journal of Neuroscience.

[28]  S. Zola-Morgan,et al.  Concurrent discrimination learning of monkeys after hippocampal, entorhinal, or fornix lesions , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  M. Petrides,et al.  The Effects of Lesions to the Mammillary Region and the Hippocampus on Conditional Associative Learning by Rats , 1996, The European journal of neuroscience.

[30]  J. Disterhoft,et al.  Hippocampectomy disrupts trace eye-blink conditioning in rabbits. , 1990, Behavioral neuroscience.

[31]  D. Gaffan,et al.  Dissociated effects of perirhinal cortex ablation, fornix transection and amygdalectomy: evidence for multiple memory systems in the primate temporal lobe , 2004, Experimental Brain Research.

[32]  R. Church,et al.  Separation of hippocampal and amygdaloid involvement in temporal memory dysfunctions , 1987, Brain Research.

[33]  L R Squire,et al.  Amnesia, memory and brain systems. , 1997, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[34]  S. Wise,et al.  Role of the Hippocampal System in Conditional Motor Learning: Mapping Antecedents to Action , 1999, Hippocampus.

[35]  J. Rawlins,et al.  Associations across time: The hippocampus as a temporary memory store , 1985, Behavioral and Brain Sciences.

[36]  D. Schacter,et al.  Medial temporal lobe activations in fMRI and PET studies of episodic encoding and retrieval , 1999, Hippocampus.

[37]  P Alvarez,et al.  Differential effects of damage within the hippocampal region on memory for a natural, nonspatial Odor-Odor Association. , 2001, Learning & memory.

[38]  B L McNaughton,et al.  Dynamics of the hippocampal ensemble code for space. , 1993, Science.

[39]  Gordon Winocur,et al.  Functional dissociation of the hippocampus and prefrontal cortex in learning and memory , 1991, Psychobiology.

[40]  R. Ridley,et al.  Learning about rules but not about reward is impaired following lesions of the cholinergic projection to the hippocampus , 1989, Brain Research.

[41]  J. O’Keefe Do hippocampal pyramidal cells signal non‐spatial as well as spatial information? , 1999, Hippocampus.

[42]  D. Gaffan,et al.  Interhemispheric transfer of visuomotor conditional learning via the anterior corpus callosum of monkeys , 1990, Behavioural Brain Research.

[43]  R. Ridley,et al.  Evidence for a Specific Information Processing Deficit in Monkeys with Lesions of the Septohippocampal System , 1997, Cortex.

[44]  J. O’Keefe,et al.  Single unit activity in the rat hippocampus during a spatial memory task , 2004, Experimental Brain Research.

[45]  R. Passingham The hippocampus as a cognitive map J. O'Keefe & L. Nadel, Oxford University Press, Oxford (1978). 570 pp., £25.00 , 1979, Neuroscience.

[46]  Robert E. Hampson,et al.  Distribution of spatial and nonspatial information in dorsal hippocampus , 1999, Nature.

[47]  M. Mishkin,et al.  Visual recognition in monkeys: effects of transection of fornix , 2004, Experimental Brain Research.

[48]  P Alvarez,et al.  Memory consolidation and the medial temporal lobe: a simple network model. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[49]  G H Glover,et al.  Separate neural bases of two fundamental memory processes in the human medial temporal lobe. , 1997, Science.

[50]  D. S. Olton,et al.  Effects of fornix transection and cingulate cortical ablation on spatial memory in rhesus monkeys , 2004, Experimental Brain Research.

[51]  M. Mishkin,et al.  Differential effects of early hippocampal pathology on episodic and semantic memory. , 1997, Science.

[52]  L. Goldstein The frontal lobes and voluntary action , 1996 .

[53]  L. Squire,et al.  The Neuropsychology of Memory , 1990 .

[54]  R. Dolan,et al.  Hippocampal novelty responses studied with functional neuroimaging , 2002 .

[55]  L R Squire,et al.  Lesions of the hippocampal formation but not lesions of the fornix or the mammillary nuclei produce long-lasting memory impairment in monkeys , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[56]  D. Amaral,et al.  Cholinergic innervation of the primate hippocampal formation: II. Effects of fimbria/fornix transection , 1996, The Journal of comparative neurology.

[57]  D. Gaffan Scene-Specific Memory for Objects: A Model of Episodic Memory Impairment in Monkeys with Fornix Transection , 1994, Journal of Cognitive Neuroscience.

[58]  D. Gaffan,et al.  Monkey hippocampus and learning about spatially directed movements , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[59]  E. Maguire,et al.  Patterns of hippocampal‐cortical interaction dissociate temporal lobe memory subsystems , 2000, Hippocampus.

[60]  D. Gaffan,et al.  A comparison of the effects of fornix transection and sulcus principalis ablation upon spatial learning by monkeys , 1989, Behavioural Brain Research.

[61]  T. Robbins,et al.  Comparative effects of excitotoxic lesions of the hippocampus and septum/diagonal band on conditional visual discrimination and spatial learning , 1993, Neuropsychologia.

[62]  M. Mishkin,et al.  Visual habit formation in monkeys with neurotoxic lesions of the ventrocaudal neostriatum , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[63]  E. Tulving,et al.  Memory Systems 1994 , 1994 .

[64]  R. Sutherland,et al.  Configural association theory and the hippocampal formation: An appraisal and reconfiguration , 1995, Hippocampus.

[65]  S P Wise,et al.  Distributed modular architectures linking basal ganglia, cerebellum, and cerebral cortex: their role in planning and controlling action. , 1995, Cerebral cortex.

[66]  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.

[67]  R. Knight Contribution of human hippocampal region to novelty detection , 1996, Nature.

[68]  D. Amaral,et al.  Three Cases of Enduring Memory Impairment after Bilateral Damage Limited to the Hippocampal Formation , 1996, The Journal of Neuroscience.

[69]  D. Gaffan,et al.  Delayed Matching by Fornix-Transected Monkeys: The Sample, the Push and the Bait , 1984, The Quarterly journal of experimental psychology. B, Comparative and physiological psychology.

[70]  H. Eichenbaum,et al.  Critical role of the hippocampus in memory for sequences of events , 2002, Nature Neuroscience.

[71]  L. Jarrard What does the hippocampus really do? , 1995, Behavioural Brain Research.

[72]  L. Jarrard On the role of the hippocampus in learning and memory in the rat. , 1993, Behavioral and neural biology.

[73]  E. Tulving,et al.  Episodic and declarative memory: Role of the hippocampus , 1998, Hippocampus.

[74]  L. Nadel,et al.  The Hippocampus as a Cognitive Map , 1978 .

[75]  Louis D. Matzel,et al.  The Role of the Hippocampus in Trace Conditioning: Temporal Discontinuity or Task Difficulty? , 2001, Neurobiology of Learning and Memory.

[76]  T. Bussey,et al.  Fornix transection impairs conditional visuomotor learning in tasks involving nonspatially differentiated responses. , 2002, Journal of neurophysiology.

[77]  R. Church,et al.  Hippocampus, time, and memory. , 1984, Behavioral neuroscience.

[78]  David Gaffan,et al.  Idiothetic input into object-place configuration as the contribution to memory of the monkey and human hippocampus: a review , 1998, Experimental Brain Research.

[79]  David Gaffan,et al.  Against memory systems. , 2002, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

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

[81]  E A Maguire,et al.  Hippocampal Amnesia , 2001, Neurocase.

[82]  H. Kuypers,et al.  Branching cortical neurons in cat which project to the colliculi and to the pons: a retrograde fluorescent double-labeling study , 2004, Experimental Brain Research.

[83]  M. Mishkin,et al.  Visual recognition in monkeys: effects of separate vs. combined transection of fornix and amygdalofugal pathways , 2004, Experimental Brain Research.

[84]  J R Hodges,et al.  Semantic dementia: relevance to connectionist models of long-term memory. , 2001, Brain : a journal of neurology.

[85]  Elisabeth A. Murray,et al.  Role of the hippocampus plus subjacent cortex but not amygdala in visuomotor conditional learning in rhesus monkeys. , 1996, Behavioral neuroscience.

[86]  R. O’Reilly,et al.  Computational principles of learning in the neocortex and hippocampus , 2000, Hippocampus.

[87]  R. Saunders,et al.  Effects of Fornix Transection upon Associative Memory in Monkeys: Role of the Hippocampus in Learned Action , 1984, The Quarterly journal of experimental psychology. B, Comparative and physiological psychology.

[88]  J. Aggleton,et al.  The effects of fornix and medial prefrontal lesions on delayed non-matching-to-sample by rats , 1993, Behavioural Brain Research.

[89]  D. Bannerman,et al.  Conditional discriminations based on external and internal cues in rats with cytotoxic hippocampal lesions. , 2001, Behavioral neuroscience.

[90]  M. Mishkin,et al.  A selective mnemonic role for the hippocampus in monkeys: memory for the location of objects , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[91]  D. Gaffan,et al.  Amnesia in man following transection of the fornix. A review. , 1991, Brain : a journal of neurology.

[92]  T. Robbins,et al.  Dissociable roles of the ventral, medial and lateral striatum on the acquisition and performance of a complex visual stimulus-response habit , 1991, Behavioural Brain Research.

[93]  H. Eichenbaum,et al.  Memory, amnesia, and the hippocampal system , 1993 .

[94]  M. Witter,et al.  Organization of the projections from the subiculum to the ventral striatum in the rat. A study using anterograde transport of Phaseolus vulgaris leucoagglutinin , 1987, Neuroscience.

[95]  H Eichenbaum,et al.  The hippocampus and transverse patterning guided by olfactory cues. , 1998, Behavioral neuroscience.

[96]  J. N. P. Rawlins,et al.  The effects of hippocampal lesions upon spatial and non-spatial tests of working memory , 1986, Behavioural Brain Research.

[97]  J. Murre TraceLink: A model of amnesia and consolidation of memory , 1996, Hippocampus.

[98]  James L. McClelland,et al.  Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory. , 1995, Psychological review.

[99]  N. Stanhope,et al.  Temporal and spatial context memory in patients with focal frontal, temporal lobe, and diencephalic lesions , 1997, Neuropsychologia.

[100]  Daniel L. Schacter,et al.  What are the memory systems of 1994 , 1994 .

[101]  M. W. Brown,et al.  Episodic memory, amnesia, and the hippocampal–anterior thalamic axis , 1999, Behavioral and Brain Sciences.

[102]  S. Tonegawa,et al.  CA1-specific N-methyl-d-aspartate receptor knockout mice are deficient in solving a nonspatial transverse patterning task , 2001, Proceedings of the National Academy of Sciences of the United States of America.