Hippocampal long-term depression and long-term potentiation encode different aspects of novelty acquisition.

The hippocampus is required for encoding spatial information. Little is known however, about how different attributes of learning are related to different types of synaptic plasticity. Here, we investigated the association between long-term depression (LTD) and long-term potentiation, both cellular models for learning, and novelty exploration. We found that exploration of a new environment containing unfamiliar objects and/or familiar objects in new locations facilitated LTD, whereas exploration of the new environment itself, in the absence of objects, impaired LTD. Furthermore, we found this phenomenon to be modulated by 5-hydroxytryptamine 4 receptor activation. In contrast, long-term potentiation was facilitated by exploration of an empty novel environment, but simultaneous object exploration caused depotentiation. We also found that no further LTD could be induced. These findings support a decisive role for LTD in the acquisition of object-place configuration and consolidate its candidacy as a learning mechanism.

[1]  Malcolm W. Brown,et al.  Different Contributions of the Hippocampus and Perirhinal Cortex to Recognition Memory , 1999, The Journal of Neuroscience.

[2]  J. Lisman,et al.  Storage, recall, and novelty detection of sequences by the hippocampus: Elaborating on the SOCRATIC model to account for normal and aberrant effects of dopamine , 2001, Hippocampus.

[3]  W. Abraham,et al.  Induction and Experience-Dependent Consolidation of Stable Long-Term Potentiation Lasting Months in the Hippocampus , 2002, The Journal of Neuroscience.

[4]  R. Morris,et al.  Impaired spatial learning after saturation of long-term potentiation. , 1998, Science.

[5]  S. Sara,et al.  Novelty seeking behavior in the rat is dependent upon the integrity of the noradrenergic system. , 1995, Brain research. Cognitive brain research.

[6]  H. Simon,et al.  Enhancement of place and object recognition memory in young adult and old rats by RS 67333, a partial agonist of 5-HT4 receptors , 2001, Neuropharmacology.

[7]  J. Frey,et al.  Bidirectional modulation of long-term potentiation by novelty-exploration in rat dentate gyrus , 2003, Neuroscience Letters.

[8]  E. Marchetti-Gauthier,et al.  5-HT4 receptors: long-term blockade of K+ channels and effects on olfactory memory. , 1998, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

[9]  F. Dauphin,et al.  RS 67333 and D-cycloserine accelerate learning acquisition in the rat , 2001, Neuropharmacology.

[10]  S. Tonegawa,et al.  The Essential Role of Hippocampal CA1 NMDA Receptor–Dependent Synaptic Plasticity in Spatial Memory , 1996, Cell.

[11]  P. Andersen,et al.  Association between brain temperature and dentate field potentials in exploring and swimming rats. , 1993, Science.

[12]  J. Bockaert,et al.  Differential modulation of the 5-HT4 receptor agonists and antagonist on rat learning and memory , 2000, Neuropharmacology.

[13]  M. Bear Homosynaptic long-term depression: a mechanism for memory? , 1999, Proceedings of the National Academy of Sciences of the United States of America.

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

[15]  Malcolm W. Brown,et al.  Recognition memory: What are the roles of the perirhinal cortex and hippocampus? , 2001, Nature Reviews Neuroscience.

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

[17]  B. Derrick,et al.  NMDA receptor antagonists sustain LTP and spatial memory: active processes mediate LTP decay , 2002, Nature Neuroscience.

[18]  M. Bear,et al.  A synaptic basis for memory storage in the cerebral cortex. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[19]  Donald A. Wilson,et al.  The fundamental role of memory in olfactory perception , 2003, Trends in Neurosciences.

[20]  A. Meneses,et al.  Effects of 5-HT4 Receptor Agonists and Antagonists in Learning , 1997, Pharmacology Biochemistry and Behavior.

[21]  W. K. Cullen,et al.  Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty , 2003, Nature Neuroscience.

[22]  D. Gaffan,et al.  Interaction of Perirhinal Cortex with the Fornix–Fimbria: Memory for Objects and “Object-in-Place” Memory , 1996, The Journal of Neuroscience.

[23]  Paul E. Gilbert,et al.  Role of the rodent hippocampus in paired-associate learning involving associations between a stimulus and a spatial location. , 2002, Behavioral neuroscience.

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

[25]  L. Squire,et al.  Structure and function of declarative and nondeclarative memory systems. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[26]  Tadaharu Tsumoto,et al.  Long-term depression in cerebral cortex: a possible substrate of “forgetting” that should not be forgotten , 1993, Neuroscience Research.

[27]  G. Rondouin,et al.  5-HT4 Receptors Improve Social Olfactory Memory in the Rat , 1997, Neuropharmacology.

[28]  D. Manahan‐Vaughan,et al.  Novelty acquisition is associated with induction of hippocampal long-term depression. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

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

[30]  Michael J. Rowan,et al.  Spatial exploration induces a persistent reversal of long-term potentiation in rat hippocampus , 1998, Nature.

[31]  U. Frey,et al.  Hippocampal synaptic plasticity: role in spatial learning or the automatic recording of attended experience? , 1997, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[32]  Burton S. Rosner,et al.  Neuropharmacology , 1958, Nature.

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

[34]  Denise Manahan-Vaughan,et al.  Group 1 and 2 Metabotropic Glutamate Receptors Play Differential Roles in Hippocampal Long-Term Depression and Long-Term Potentiation in Freely Moving Rats , 1997, The Journal of Neuroscience.