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Hippocampal–anterior thalamic pathways for memory: uncovering a network of direct and indirect actions
John P. Aggleton, Shane M. O’Mara, Seralynne D. Vann and 3 more
European Journal of Neuroscience · 2010 · Review
doi:10.1111/j.1460-9568.2010.07251.x
Abstract
This review charts recent advances from a variety of disciplines that create a new perspective on why the multiple hippocampal–anterior thalamic interconnections are together vital for human episodic memory and rodent event memory. Evidence has emerged for the existence of a series of parallel temporal–diencephalic pathways that function in a reciprocal manner, both directly and indirectly, between the hippocampal formation and the anterior thalamic nuclei. These extended pathways also involve the mammillary bodies, the retrosplenial cortex and parts of the prefrontal cortex. Recent neuropsychological findings reveal the disproportionate importance of these hippocampal–anterior thalamic systems for recollective rather than familiarity‐based recognition, while anatomical studies highlight the precise manner in which information streams are kept separate but can also converge at key points within these pathways. These latter findings are developed further by electrophysiological stimulation studies showing how the properties of the direct hippocampal–anterior thalamic projections are often opposed by the indirect hippocampal projections via the mammillary bodies to the thalamus. Just as these hippocampal–anterior thalamic interactions reflect an interdependent system, so it is also the case that pathology in one of the component sites within this system can induce dysfunctional changes to distal sites both directly and indirectly across the system. Such distal effects challenge more traditional views of neuropathology as they reveal how extensive covert pathology might accompany localised overt pathology, and so impair memory.
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References 179
- 1.
Adlam A-L, Malloy M, Mishkin M, Vargha-Khadem F. Dissociation between recognition and recall in developmental amnesia. Neuropsychologia. 2009;47:2207-2210.
Not in our library10.1016/j.neuropsychologia.2009.01.038
- 2.
Aggleton JP. Understanding anterograde amnesia: disconnections and hidden lesions. Q. J. Exp. Psychol. 2008;61:1441-1471.
Not in our library10.1080/17470210802215335
- 3.
Aggleton JP, Brown MW. Episodic memory, amnesia and the hippocampal–anterior thalamic axis. Behav. Brain Sci. 1999;22:425-444.
Not in our library
- 4.
Aggleton JP, Brown MW, Squire LR, Schacter D. Integrating systems for event memory: testing the contribution of the fornix. Neuropsychology of Memory. 2002;377-394.
Not in our library
- 5.
Aggleton JP, Brown MW. Interleaving brain systems for episodic and recognition memory. Trends Cogn. Sci. 2006;10:455-463.
Not in our library10.1016/j.tics.2006.08.003
- 6.
Aggleton JP, Mishkin M. Mamillary-body lesions and visual recognition in monkeys. Exp. Brain Res. 1985;58:190-197.
Not in our library10.1007/bf00238967
- 7.
Aggleton JP, Sahgal A. The contribution of the anterior thalamic nuclei to anterograde amnesia. Neuropsychologia. 1993;31:1001-1019.
Not in our library10.1016/0028-3932(93)90029-y
- 8.
Aggleton JP, Saunders RC. The relationships between temporal lobe and diencephalic structures implicated in anterograde amnesia. Memory. 1997;5:49-71.
Not in our library10.1080/741941143
- 9.
Aggleton JP, Desimone R, Mishkin M. The origin, course, and termination of the hippocampo-thalamic projections in the macaque. J. Comp. Neurol. 1986;243:409-422.
Not in our library10.1002/cne.902430310
- 10.
Aggleton JP, Hunt PR, Shaw C. The effects of mammillary body and combined amygdalar-fornix lesions on tests of delayed nonmatching-to-sample. Behav. Brain Res. 1990;40:145-157.
Not in our library10.1016/0166-4328(90)90006-z
- 11.
Aggleton JP, Neave NJ, Nagle S, Hunt PR. A comparison of the effects of anterior thalamic, mamillary body and fornix lesions on reinforced spatial alternation. Behav. Brain Res. 1995;68:91-101.
Not in our library10.1016/0166-4328(94)00163-a
- 12.
Aggleton JP, McMackin D, Carpenter K, Hornak J, Kapur N, Halpin S, Wiles CM, Kamel H, Brennan P, Gaffan D. Differential effects of colloid cysts in the third ventricle that spare or compromise the fornix. Brain. 2000;123:800-815.
Not in our library10.1093/brain/123.4.800
- 13.
Aggleton JP, Vann SD, Denby C, Dix S, Mayes AR, Roberts N, Yonelinas AP. Sparing of the familiarity component of recognition memory in a patient with hippocampal pathology. Neuropsychologia. 2005a;43:1810-1823.
Not in our library10.1016/j.neuropsychologia.2005.01.019
- 14.
Aggleton JP, Vann SD, Saunders RC. Projections from the hippocampal region to the mammillary bodies in macaque monkeys. Eur. J. Neurosci. 2005b;22:2519-2530.
Not in our library10.1111/j.1460-9568.2005.04450.x
- 15.
Aggleton JP, Sanderson DJ, Pearce JM. Structural learning and the hippocampus. Hippocampus. 2007;17:723-734.
Not in our library10.1002/hipo.20323
- 16.
Aggleton JP, Poirier GL, Aggleton HS, Vann SD, Pearce JM. Lesions of the fornix and anterior thalamic nuclei dissociate different aspects of hippocampal-dependent spatial learning: implications for the neural basis of scene learning. Behav. Neurosci. 2009;123:504-519.
Not in our library10.1037/a0015404
- 17.
Albasser MM, Poirier GL, Warburton EC, Aggleton JP. Hippocampal lesions halve immediate-early gene protein counts in retrosplenial cortex activity: distal dysfunctions in a spatial memory system. Eur. J. Neurosci. 2007;26:1254-1266.
Not in our library10.1111/j.1460-9568.2007.05753.x
- 18.
Albasser M, Poirier GL, Aggleton JP. Qualitatively different modes of perirhinal-hippocampal engagement when rats explore novel vs. familiar objects as revealed by c-Fos imaging. Eur. J. Neurosci. 2010;31:134-147.
Not in our library10.1111/j.1460-9568.2009.07042.x
- 19.
Albo Z, Viana Di Prisco G, Vertes RP. Anterior thalamic unit discharge profiles and coherence with hippocampal theta rhythm. Thalamus Relat. Syst. 2003;2:133-144.
Not in our library
- 20.
Amaral DG, Cowan WM. Subcortical afferents to the hippocampal formation in the monkey. J. Comp. Neurol. 1980;189:573-591.
Not in our library10.1002/cne.901890402
- 21.
Bachevalier J, Saunders RC, Mishkin M. Visual recognition in monkeys: effects of transection of fornix. Exp. Brain Res. 1985;57:547-553.
Not in our library10.1007/bf00237841
- 22.
Barnes CA. Involvement of LTP in memory: are we ‘searching under the street light’? Neuron. 1995;15:751-754.
Not in our library10.1016/0896-6273(95)90166-3
- 23.
Bassett JP, Taube JS, Wiener SI, Taube JS. Head direction signal generation: ascending and descending information streams. Head Direction and Cells and the Neural Mechanisms of Spatial Orientation. 2005;83-109.
Not in our library
- 24.
Bastin C, Van der Linden M, Charnallet A, Denby C, Montaldi M, Roberts N, Mayes AR. Dissociation between recall and recognition memory performance in an amnesic patient with hippocampal damage following carbon monoxide poisoning. Neurocase. 2004;10:330-344.
Not in our library10.1080/13554790490507650
- 25.
Bear MF. Bidirectional synaptic plasticity: from theory to reality. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2003;358:649-655.
Not in our library10.1098/rstb.2002.1255
- 26.
Bird CM, Burgess N. The hippocampus and memory; Insights from spatial processing. Nat. Rev. Neurosci. 2008;9:182-194.
Not in our library10.1038/nrn2335
- 27.
Bland BH, Konopacki J, Kirk IJ, Oddie SD, Dickson CT. Discharge patterns of hippocampal theta-related cells in the caudal diencephalon of the urethan-anesthetized rat. J. Neurophysiol. 1995;74:322-333.
Not in our library10.1152/jn.1995.74.1.322
- 28.
Bliss TVP, Collingridge GL. A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 1993;361:31-39.
Not in our library10.1038/361031a0
- 29.
Brown MW, Aggleton JP. Recognition memory; What are the roles of the perirhinal cortex and hippocampus? Nat. Rev. Neurosci. 2001;2:51-61.
Not in our library10.1038/35049064
- 30.
Burgess N, Maguire EA, O’Keefe J. The human hippocampus and spatial and episodic memory. Neuron. 2002;35:625-641.
Not in our library10.1016/s0896-6273(02)00830-9
- 31.
Bussey TJ, Warburton EC, Aggleton JP, Muir JL. Fornix lesions can facilitate acquisition of the transverse patterning task: a challenge for “configural” theories of hippocampal function. J. Neurosci. 1998;18:1622-1631.
Not in our library10.1523/jneurosci.18-04-01622.1998
- 32.
Bussey TJ, Dias R, Redhead ES, Pearce JM, Muir JL, Aggleton JP. Intact negative patterning in rats with fornix or combined perirhinal and postrhinal cortex lesions. Exp. Brain Res. 2000a;134:506-519.
Not in our library10.1007/s002210000481
- 33.
Bussey TJ, Duck JD, Muir JL, Aggleton JP. Distinct patterns of behavioural impairments resulting from fornix transection or neurotoxic lesions of the perirhinal and postrhinal cortices in the rat. Behav. Brain Res. 2000b;111:187-202.
Not in our library10.1016/s0166-4328(00)00155-8
- 34.
Bussey TJ, Saksida LM, Murray EA. Perirhinal cortex resolves feature ambiguity in complex visual discriminations. Eur. J. Neurosci. 2002;15:365-374.
Not in our library10.1046/j.0953-816x.2001.01851.x
- 35.
Buzsáki G. Theta oscillations in the hippocampus. Neuron. 2002;33:325-340.
Not in our library10.1016/s0896-6273(02)00586-x
- 36.
Byatt G, Dalrymple-Alford JC. Both anteromedial and anteroventral thalamic lesions impair radial-maze learning in rats. Behav. Neurosci. 1996;110:1335-1348.
Not in our library10.1037//0735-7044.110.6.1335
- 37.
Byrne P, Becker S, Burgess N. Remembering the past and imagining the future: a neural model of spatial memory and imagery. Psychol. Rev. 2007;114:340-375.
Not in our library10.1037/0033-295x.114.2.340
- 38.
Carlesimo GA, Serra L, Fadda L, Cherubini A, Bozzali M, Caltagirone C. Bilateral damage to the mammillo-thalamic tract impairs recollection but not familiarity in the recognition process: a single case investigation. Neuropsychologia. 2007;45:2467-2479.
Not in our library10.1016/j.neuropsychologia.2007.03.025
- 39.
Cassel J-C, Duconseille E, Jeltsch H, Will B. The fimbria-fornix/cingular bundle pathways: a review of neurochemical and behavioural approaches using lesions and transplantation techniques. Prog. Neurobiol. 1997;51:663-716.
Not in our library10.1016/s0301-0082(97)00009-9
- 40.
Cassel J-C, Sassel S, Galani R, Kelche C, Will B, Jarrard L. Fimbria-fornix vs selective hippocampal lesions in rats: effects on locomotor activity and spatial learning and memory. Neurobiol. Learn. Mem. 1998;69:22-45.
Not in our library10.1006/nlme.1997.3807
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