Anterograde and retrograde memory for object discriminations and places in rats with perirhinal cortex lesions

Behavioural Brain Research

Volumn 114, Issue 1-2, 2000, Pages 119-134

  Mumby, Dave G ^a   Glenn, Melissa J ^a  

^a Gina Cody School of Engineering and Computer Science   (Canada)

Author keywords

Consolidation; Object discrimination; Perirhinal cortex; Rats; Retrograde amnesia; Spatial memory; Water maze

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANTEROGRADE AMNESIA; ARTICLE; BRAIN CORTEX; BRAIN INJURY; CONTROLLED STUDY; MALE; MEMORY; MEMORY CONSOLIDATION; NONHUMAN; PRIORITY JOURNAL; RAT; RECOGNITION; RETROGRADE AMNESIA; SPATIAL MEMORY; VISUAL DISCRIMINATION;

AMNESIA, ANTEROGRADE; AMNESIA, RETROGRADE; ANIMAL; DISCRIMINATION (PSYCHOLOGY); DISCRIMINATION LEARNING; ELECTRIC STIMULATION; ELECTRODES; FORM PERCEPTION; HIPPOCAMPUS; MALE; MAZE LEARNING; MEMORY; RATS; RATS, LONG-EVANS; STEREOTAXIC TECHNIQUES; SUPPORT, NON-U.S. GOV'T;

EID: 0034283606     PISSN: 01664328     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-4328(00)00217-5     Document Type: Article

References (49)

1. Aggleton J.P., Keen S., Warburton E.C., Bussey T.J. Extensive cytotoxic lesions involving both the rhinal cortices and area TE impair recognition but spare spatial alternation in the rat. Brain Res. Bull. 43:1997;279-287.
2. Astur R.S., Mumby D.G., Sutherland R.J. Perirhinal cortex damage: effects on acquisition and retention of object and place discriminations in rats. Soc. Neurosci. Abstr. 21:1995;1935.
3. Buckley M.J., Gaffan D. Impairment of visual object-discrimination learning after perirhinal cortex ablation. Behav. Neurosci. 111:1997;467-475.
4. Burwell R.D., Witter M.P., Amaral D.G. Perirhinal and postrhinal cortices of the rat: a review of the neuroanatomical literature and comparison with findings from the monkey brain. Hippocampus. 5:1995;390-408.
5. Bussey T.J., Muir J.L., Aggleton J.P. Functionally dissociating aspects of event memory: the effects of combined perirhinal and postrhinal cortex lesions on object and place memory in the rat. J. Neurosci. 19:1999;495-502.
6. Deacon T.W., Eichenbaum H., Rosenberg P., Eckmann K.W. Afferent connections of the perirhinal cortex in the rat. J. Comp. Neurol. 220:1983;168-190.
7. Eacott M.J., Gaffan D., Murray E.A. Preserved recognition memory for small sets, and impaired stimulus identification for large sets following rhinal cortex ablation in monkeys. Eur. J. Neurosci. 6:1994;1466-1478.
8. Eichenbaum H., Otto T., Cohen N.J. Two functional components of the hippocampal memory system. Behav. Brain Sci. 17:1994;449-518.
9. Ennaceur A., Neave N., Aggleton J.P. Neurotoxic lesions of the perirhinal cortex do not mimic the behavioural effects of fornix transection in the rat. Behav. Brain Res. 80:1996;9-25.
10. Gaffan D., Murray E.A. Monkeys with rhinal cortex lesions succeed in object discrimination learning despite 24-hour intertrial intervals and fail at match to sample despite double sample presentations. Behav. Neurosci. 106:1992;30-38.
11. Glenn M.J., Mumby D.G. Place- and object-recognition deficits following lesions of the hippocampus or perirhinal cortex in rats: a double dissociation. Soc. Neurosci. Abstr. 22:1996;1120.
12. Glenn M.J., Mumby D.G. Perirhinal cortex lesions do not impair allocentric spatial-working memory in rats. Behav. Neurosci. 112:1998;1353-1365.
13. Good M., Honey R.C. Conditioning and contextual retrieval in hippocampal rats. Behav. Neurosci. 105:1991;499-509.
14. Kim J.J., Fanselow M.S. Modality-specific retrograde amnesia for fear. Science. 256:1992;675-677.
15. Kolb B., Buhrmann K., McDonald R.J., Sutherland R.J. Dissociation of the medial prefrontal, posterior parietal, and posterior temporal cortex for spatial navigation and recognition memory in the rat. Cerebral Cortex. 6:1994;664-680.
16. Kornecook T.J., Liu M., Duva C.A., Anzarut A., Pinel J.P.J. Effects of perirhinal or rhinal cortex lesions on object-memory tasks in rats. Soc. Neurosci. Abstr. 21:1995;1935.
17. Kosel K.C., Van Hoesen G.W., Rosene D.L. A direct projection from the perirhinal cortex (area 35) to the subiculum in the rat. Brain Res. 269:1983;347-351.
18. Liu P., Bilkey D.K. Excitotoxic lesions centered on perirhinal cortex produce delay-dependent deficits in a test of spatial memory. Behav. Neurosci. 3:1998;512-524.
19. Mayes A.R. Memory and amnesia. Behav. Brain Res. 66:1995;29-36.
20. McClelland J.L., McNaughton B.L., O'Reilly R.C. Why are there complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory. Psychol. Rev. 102:1995;419-457.
21. Meunier M., Bachevalier J., Mishkin M., Murray E.A. Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys. J. Neurosci. 13:1993;5418-5432.
22. Mishkin M., Murray E.A. Stimulus recognition. Curr. Opin. Neurobiol. 4:1994;200-206.
23. Morris R.G.M. Spatial localization does not require the presence of local cues. Learn. Motiv. 12:1981;239-260.
24. Morris M., Garrud P., Rawlins J.N.P., O'Keefe J. Place navigation impaired in rats with hippocampal lesions. Nature. 297:1982;681-683.
25. Mumby D.G., Astur R.S., Sutherland R.J., Weisend M.P. Retrograde amnesia and selective damage to the hippocampal formation: memory for places and object discriminations. Behav. Brain Res. 106:1999;97-107.
26. Mumby D.G., Pinel J.P.J., Kornecook T.J., Shen M.J., Redila V.A. Memory deficits following lesions of hippocampus or amygdala in rats: assessment by an object-memory test battery. Psychobiology. 23:1995;26-36.
27. Mumby D.G., Pinel J.P.J. Rhinal cortex lesions and object recognition in rats. Behav. Neurosci. 108:1994;11-18.
28. Mumby D.G., Pinel J.P.J., Wood E.R. Nonrecurring-items delayed nonmatching-to-sample in rats: a new paradigm for testing nonspatial working memory. Psychobiology. 18:1990;321-326.
29. Mumby D.G., Wood E.R., Duva C.A., Kornecook T.J., Phillips A.G., Pinel J.P.J. Ischemia-induced object-recognition deficits in rats are prevented by hippocampal ablation before or soon after ischemia. Behav. Neurosci. 110:1996;266-281.
30. Mumby D.G., Wood E.R., Pinel J.P.J. Object-recognition memory is only mildly impaired in rats with lesions of the hippocampus and amygdala. Psychobiology. 20:1992;18-27.
31. Murray E.A., Mishkin M. Object recognition and location memory in monkeys with excitotoxic lesions of the amygdala and hippocampus. J. Neurosci. 18:1998;6568-6582.
32. Nadel L., Moscovitch M. Memory consolidation, retrograde amnesia, and the hippocampal complex. Curr. Opin. Neurobiol. 7:1997;217-227.
33. Nadel L., Wilner J. Context and conditioning: a place for space. Physiol. Psychol. 8:1980;218-228.
34. Nagahara A.H., Otto T., Gallagher M. Entorhinal-perirhinal lesions impair performance of rats on two versions of place learning in the Morris water maze. Behav. Neurosci. 109:1995;3-9.
35. Paxinos G., Watson C. The Rat Brain in Stereotaxic Coordinates. 1986;Academic Press, Toronto.
36. Phillips R.G., LeDoux J.E. Lesions of the dorsal hippocampal formation interfere with background but not foreground contextual fear conditioning. Learn. Mem. 1:1994;34-44.
37. Rothblat L.A., Kromer L.F. Object recognition memory in the rat: the role of the hippocampus. Behav. Brain Res. 42:1991;25-32.
38. Salmon D.P., Zola-Morgan S., Squire L.R. Retrograde amnesia following combined hippocampus-amygdala lesions in monkeys. Psychobiology. 15:1987;37-47.
39. Squire L.R. Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. Psychol. Rev. 99:1992;195-231.
40. Sutherland R.J., Whishaw I.Q., Kolb B. A behavioral analysis of spatial localization following electrolytic, kainate- or colchicine-induced damage to the hippocampal formation in the rat. Behav. Brain Res. 7:1983;133-153.
41. Suzuki W.A., Amaral D.G. Cortical inputs to the CA1 field of the monkey hippocampus originate from the perirhinal and parahippocampal cortex but not from area TE. Neurosci. Lett. 115:1990;43-48.
42. Thornton J.A., Rothblat L.A., Murray E.A. Rhinal cortex removal produces amnesia for preoperatively learned discrimination problems but fails to disrupt postoperative acquisition and retention in rhesus monkeys. J. Neurosci. 17:1997;8536-8549.
43. Whishaw I.Q., McKenna J.E., Maaswinkel H. Hippocampal lesions and path integration. Curr. Opin. Neurobiol. 7:1997;228-234.
44. Wiig K.A., Bilkey D.K. Subtotal perirhinal cortex lesions increase exploratory behaviour in the rat without producing deficits in the Morris water maze. Psychobiology. 22:1994;195-202.
45. Wiig K.A., Bilkey D.K. The effects of perirhinal cortical lesions on spatial reference memory in the rat. Behav. Brain Res. 63:1994;101-109.
46. Wiig K.A., Bilkey D.K. Lesions of rat perirhinal cortex exacerbate the memory deficit observed following damage to the fimbria-fornix. Behav. Neurosci. 109:1995;620-630.
47. Witter M.P., Groenewegen H.J., Lopes da Silva F.H., Lohman A.H.M. Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region. Prog. Neurobiol. 33:1989;161-254.
48. Zola-Morgan S., Squire L.R. The primate hippocampal formation: evidence for a time-limited role in memory storage. Science. 250:1990;288-290.
49. Zola-Morgan S., Squire L.R., Amaral D.G., Suzuki W.A. Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment. J. Neurosci. 9:1989;4355-4370.