The roles of perirhinal cortex, postrhinal cortex, and the fornix in memory for objects, contexts, and events in the rat

Quarterly Journal of Experimental Psychology Section B: Comparative and Physiological Psychology

Volumn 58, Issue 3-4, 2005, Pages 202-217

  Eacott, M J ^a   Gaffan, E A ^b  

^a DURHAM UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF READING   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; BRAIN FORNIX; CONFERENCE PAPER; CONTRAST SENSITIVITY; ENTORHINAL CORTEX; MEMORY; NERVE TRACT; PHYSIOLOGY; RAT; TEMPORAL LOBE;

ANIMALS; CONTRAST SENSITIVITY; ENTORHINAL CORTEX; FORNIX (BRAIN); MEMORY; NEURAL PATHWAYS; RATS; TEMPORAL LOBE;

EID: 23844544995     PISSN: 02724995     EISSN: None     Source Type: Journal    
DOI: 10.1080/02724990444000203     Document Type: Conference Paper

References (70)

1. Aggleton, J. P., & Brown, M. W. (1999). Episodic memory, amnesia and the hippocampal-anterior thalamic axis. Behavioural and Brain Sciences, 22, 425-189.
2. Aggleton, J. P., & Brown, M. W. (this issue). Contrasting hippocampal and perirhinal cortex function using immediate early gene imaging. Quarterly Journal of Experimental Psychology, 58B, 218-233.
3. Bird, L. R., Roberts, W. A., Abroms, B., Kit, K. A., & Crupi, C. (2003). Spatial memory for food hidden by rats (Rattus norvegicus) on the radial maze. Studies of memory for where, what, and when. Journal of Comparative Psychology, 117, 176-187.
4. Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2000). Contributions of postrhinal and perirhinal cortex to contextual information processing. Behavioral Neuroscience, 114, 882-894.
5. Bucci, D. J., Saddoris, M. P., & Burwell, R. D. (2002). Contextual fear discrimination is impaired by damage to the postrhinal or perirhinal cortex. Behavioral Neuroscience, 116, 479-488.
6. Buckley, M. J. (this issue). The role of the perirhinal cortex and hippocampus in learning, memory, and perception. Quarterly Journal of Experimental Psychology, 58B, 264-268.
7. Buckley, M. J., Booth, M. C. A., Rolls, E. T., & Gaffan, D. (2001). Selective perceptual impairments after perirhinal cortex ablation. Journal of Neuroscience, 21, 9824-9836.
8. Buckley, M. J., & Gaffan, D. (1998a). Perirhinal cortex ablation impairs configural learning and paired-associate learning equally. Neuropsychologia, 36, 535-546.
9. Buckley, M. J., & Gaffan, D. (1998b). Perirhinal cortex ablation impairs visual object identification. Journal of Neuroscience, 18, 2268-2275.
10. Buckley, M. J., Gaffan, D., & Murray, E. A. (1997). Functional double dissociation between two inferior temporal cortical areas. Perirhinal cortex versus middle temporal gyrus. Journal of Neurophysiology, 77, 587-598.
11. Burwell, R. D., & Amaral, D. G. (1998a). Cortical afferents of the perirhinal, postrhinal and entorhinal cortices of the rat. Journal of Comparative Neurology, 398, 179-205.
12. Burwell, R. D., & Amaral, D. G. (1998b). Perirhinal and postrhinal cortices of the rat. Interconnectivity and connections with the entorhinal cortex. Journal of Comparative Neurology, 391, 293-321.
13. Burwell, R. D., & Hafeman, D. M. (2003). Positional firing properties of postrhinal cortex neurons. Neuroscience, 119, 577-588.
14. Burwell, R. D., Saddoris, M. P., Bucci, D. J., & Wiig, K. A. (2004). Corticohippocampal contributions to spatial and contextual learning. Journal of Neuroscience, 24, 3826-3836.
15. Burwell, R. D., Witter, M. P., & Amaral, D. G. (1995). The perirhinal and postrhinal cortices of the rat: A review of the neuroanatomical literature and comparison with findings from the monkey brain. Hippocampus, 5, 390-408.
16. Bussey, T. J., Dias, R., Amin, E., Muir, J. L., & Aggleton, J. P. (2001). Perirhinal cortex and place-object conditional learning in the rat. Behavioral Neuroscience, 115, 776-785.
17. Bussey, T. J., & Saksida, L. M. (2002). The organization of visual object representations; a connectionist model of effects of lesions in perirhinal cortex. European Journal of Neuroscience, 15, 355-364.
18. Bussey, T. J., Saksida, L. M., & Murray, E. A. (2002). Perirhinal cortex resolves feature ambiguity in complex visual discriminations. European Journal of Neuroscience, 15, 365-374.
19. Bussey, T. J., Saksida, L. M., & Murray, E. A. (2003). Impairments in visual discrimination after perirhinal cortex lesions, testing 'declarative' vs. 'perceptual-mnemonic' views of perirhinal cortex function. European Journal of Neuroscience, 17, 649-660.
20. Bussey T. J., Saksida, L. M., & Murray, E. A. (this issue). The perceptual-mnemonic/feature conjunction model of perirhinal cortex function. Quarterly Journal of Experimental Psychology, 58B, 269-282.
21. Clayton, N. S., Bussey, T. J., Emery, N. J., & Dickinson, A. (2003). Prometheus to Proust, the case for behavioural criteria for mental time travel. Trends in Cognitive Science, 7, 346-347.
22. Clayton, N. S., & Dickinson, A. (1998). What, where and when, episodic like memory during cache recovery by scrub jays. Nature, 395, 272-274.
23. Clayton, N. S., Griffiths, D. P., Emory, N.J., & Dickinson, A. (2001). Elements of episodic-like memory in animals. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 356, 1483-1491.
24. Cummings, J. L., Tomiyasu, S., Read, S., & Benson, D. F. (1984). Amnesia with hippocampal lesions after cardiopulmonary arrest. Neurology, 34, 679-681.
25. Dellu, F., Fauchey, V., LeMoal, M., & Simon, H. (1997). Extension of a new two-trial memory task in the rat. Influence of environmental context on recognition processes. Neurobiology of Learning and Memory, 67, 112-120.
26. Dix, S. L., & Aggleton, J. P. (1999). Extending the spontaneous preference test of recognition; evidence of object-location and object-context recognition. Behavioural Brain Research, 99, 191-200.
27. Eacott, M. J., Gaffan, D., & Murray, E. A. (1994). Preserved recognition memory for small sets and impaired stimulus identification for large sets following rhinal cortex ablations in monkeys. European Journal of Neuroscience, 6, 1466-1478.
28. Eacott, M. J., & Heywood, C. A. (1995). Perception and memory, action and interaction. Critical Reviews in Neurobiology, 9, 311-320.
29. Eacott, M. J., & Norman, G. (2004). Integrated memory for object, place and context in rats: A possible model of episodic-like memory in rats? Journal of Neuroscience, 24, 1948-1953.
30. Eacott, M. J., Machin, P. E., & Gaffan, E. A. (2001). Elemental and configural visual discrimination learning following lesions to perirhinal cortex in the rat. Behavioural Brain Research, 124, 55-70.
31. Eacott, M. J., Norman, G., & Gaffan, E. A. (2003). The role of perirhinal cortex in visual discrimination learning for visual secondary reinforcement in rats. Behavioral Neuroscience, 117, 1318-1325.
32. Ennaceur, A., & Delacour, J. (1988). A new one-trial test for neurobiological studies of memory in rats. 1. Behavioral-data. Behavioural Brain Research, 31, 47-59.
33. Ennaceur, A., & Meliani, K. (1992). A new one-trial test for neurobiological studies of memory in rats. 3. Spatial vs. nonspatial working memory. Behavioural Brain Research, 51, 83-92.
34. Ennaceur, A., Neave, N., & Aggleton, J. P. (1997). Spontaneous object recognition and object location memory in rats; the effects of lesions in the cingulate cortices, the medial prefrontal cortex, the cingulum bundle and the fornix. Experimental Brain Research, 113, 509-519.
35. Ergorul, C., & Eichenbaum, H. (2004). The hippocampus and memory for "What", "Where", and "When". Learning and Memory, 11, 397-405.
36. Fortin, N. J., Wright, S. P., & Eichenbaum, H. (2004). Recollection-like memory retrieval in rats is dependent on the hippocampus. Nature, 431, 188-191.
37. Gaffan, D. (1994). Scene-specific memory for objects: A model of episodic memory impairment in monkeys with fornix transection. Journal of Cognitive Neuroscience, 6, 305-320.
38. Gaffan, E. A., Bannerman, D. M., Warburton, E. C., & Aggleton, J. P. (2001). Rats' processing of visual scenes, effects of lesions to fornix, anterior thalamus, mamillary nuclei or the retrohippocampal region. Behavioural Brain Research, 121, 103-117.
39. Gaffan, E. A., & Eacott, M. J. (1995). A computer controlled maze environment for testing visual memory in the rat. Journal of Neuroscience Methods, 60, 23-27.
40. Gaffan, E. A., Eacott, M. J., & Simpson, E. L. (2000). Perirhinal ablation in rats selectively impairs object identification in a simultaneous visual comparison task. Behavioral Neuroscience, 114, 18-31.
41. Gaffan, E. A., Healey, A. N., & Eacott, M. J. (2004). Objects and positions in visual scenes; effects of perirhinal and postrhinal cortex lesions in the rat. Behavioral Neuroscience, 118, 992-1010.
42. Hampton, R. R. (this issue). Monkey perirhinal cortex is critical for visual memory, but not for visual perception: Reexamination of the behavioural evidence from monkeys. Quarterly Journal of Experimental Psychology, 58B, 283-299.
43. Hampton, R. R., & Schwartz, B. L. (2004). Episodic memory in nonhumans, what, and where, is when? Current Opinion in Neurobiology, 14, 192-197.
44. Hayman, R. M. A., Chakraborty, S., Anderson, M. I., & Jeffery, K. J. (2003). Context-specific acquisition of location discrimination by hippocampal place cells. European Journal of Neuroscience, 18, 2825-2834.
45. Holdstock, J. S. (this issue). The role of the human medial temporal lobe in object recognition and object discrimination. Quarterly Journal of Experimental Psychology, 58B, 326-339.
46. Holland, P. C., & Bouton, M. E. (1999). Current Opinion in Nearobiology, 9, 195-202.
47. Jeffery, K. J., Anderson, M. I., Hayman, R., & Chakraborty, S. (2004). A proposed architecture for the neural representation of spatial context. Neuroscience and Bioheliavioral Revieirs, 28, 201-218.
48. Lee, A. C. H., Barense, M. D., & Graham, K. S. (this issue). The contribution of the human medial temporal lobe to perception: Bridging the gap between animal and human studies. Quarterly Journal of Experimental Psychology, 58B, 300-325.
49. Liu, P., & Bilkey, D. K. (2001). The effect of excitotoxic lesions centered on the hippocampus or perirhinal cortex in object recognition and spatial memory tasks. Behavioral Neuroscience, 115, 94-111.
50. Malkova, L., & Mishkin, M. (2003). One-trial memory for object-place associations after separate lesions of hippocampus and posterior parahippocampal region in the monkey. Journal of Neuroscience, 23, 1956-1965.
51. Meunier, M., Bachevalier, J., Mishkin, M., & Murray, E. A. (1993). Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus-monkeys. Journal of Neuroscience, 13, 5418-5432.
52. Mumby, D. G., & Pinel, J. P. J. (1994). Rhinal cortex lesions and object recognition in rats. Behavioral Neuroscience, 108, 1-8.
53. Murray, E. A., Baxter, M. G., & Gaffan, D. (1998). Monkeys with rhinal cortex damage or neurotoxic hippocampal lesions are impaired on spatial scene learning and object reversals. Behavioral Neuroscience, 112, 1291-1303.
54. Murray, E. A., & Bussey, T. J. (1999). Perceptual-mnemonic functions of the perirhinal cortex. Trends In Cognitive Sciences, 3, 142-151
55. Murray, E. A., Bussey, T. J., Hampton, R. R., & Saksida, L. M. (2000). The parahippocampal region and object identification. Annals of the New York Academy of Sciences, 911, 166-174.
56. Norman, G., & Eacott, M. J. (2004). Impaired object recognition with increasing levels of feature ambiguity in rats with perirhinal cortex lesions. Behavioural Brain Research, 148, 79-91.
57. Norman, G., & Eacott, M. J. (2005). Dissociable effects of lesions to the perirhinal cortex and the postrhinal cortex on memory for context and objects in rats. Behavioral Neuroscience, 119, 557-566.
58. Rempel-Clower, N. L., Zola-Morgan, S., Squire, L. R., & Amaral, D. G. (1996). Three cases of enduring memory impairment following bilateral damage limited to the hippocampal formation. Journal of Neuroscience, 16, 5233-5255.
59. Scoville, W. B., & Milner, B. (1957). Loss of recent memory after bilateral hippocampal lesions. Journal of Neurology, Neurosurgery and Psychiatry, 20, 11-21.
60. Suddendorf, T., & Busby, J. (2003). Mental time travel in animals? Trends in Cognitive Science, 7, 391-396.
61. Suzuki, W. A., & Amaral, D. G. (1994). The perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents. Journal of Comparative Neurology, 350, 497-533.
62. Teng, E., Squire, L. R., & Zola, S. (1997). Different roles for the parahippocampal and perirhinal cortices in spatial reversal. Society for Neuroscience Abstracts, 23, 12.7.
63. Tulving, E. (1983). Elements of episodic memory. Oxford, UK: Clarendon Press.
64. Vann, S. D., Brown, M. W., Erichsen, J. T., & Aggleton, J. P. (2000). Fos imaging reveals differential patterns of hippocampal and parahippocampal subfield activation in rats in response to different spatial memory tests. Journal of Neuroscience, 20, 2711-2718.
65. Wan, H. M., Aggleton, J. P., & Brown, M. W. (1999). Different contributions of the hippocampus and perirhinal cortex to recognition memory. Journal of Neuroscience, 19, 1142-1148.
66. Winters, B. D., Forwood, S. E., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004). Double dissociation between the effects of peri-postrhinal cortex and hippocampal lesions on tests of object recognition and spatial memory-Heterogeneity of function within the temporal lobe. Journal of Neuroscience, 24, 5901-5908.
67. Zhu, X. O., Brown, M. W., & Aggleton, J. P. (1995a). Neuronal signalling of information important to visual recognition memory in rat rhinal and neighbouring cortices. European Journal of Neuroscience, 7, 753-765.
68. Zhu, X. O., Brown, M. W., McCabe, B. J., & Aggleton, J. P. (1995b). Effects of novelty or familiarity of visual stimuli on the expression of the immediate early gene c-fos in the rat brain. Neuroscience, 69, 821-829.
69. Zola-Morgan, S., Squire, L. R., & Amaral, D. G. (1986). Human amnesia and the medial temporal region, enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus. Journal of Neuroscience, 6, 2950-2967.
70. Zola-Morgan, S., Squire, L. R., Amaral, D. G., & Suzuki, W. A. (1994). Lesions of perirhinal cortex that spare the amygdala and hippocampal formation produce severe memory impairment. Journal of Neuroscience, 9, 4355-4370.