How does the hippocampal formation mediate memory for stimuli processed by the magnocellular and parvocellular visual pathways? Evidence from the comparison of schizophrenia and amnestic mild cognitive impairment (aMCI)

Neuropsychologia

Volumn 50, Issue 14, 2012, Pages 3193-3199

  Kéri, Szabolcs ^a,b   Szamosi, András ^a   Benedek, György ^b   Kelemen, Oguz ^c  

^a National Psychiatry Center   (Hungary)

^b UNIVERSITY OF SZEGED   (Hungary)

^c BÁCS KISKUN COUNTY TEACHING HOSPITAL   (Hungary)

Author keywords

Amnestic mild cognitive impairment; Hippocampus; Magnocellular pathway; Memory; Paired associates learning; Schizophrenia; Vision

Indexed keywords

ADULT; AMNESIA; ARTICLE; BRAIN SIZE; CLINICAL ARTICLE; COGNITION; CONTROLLED STUDY; FEMALE; HIPPOCAMPUS; HUMAN; LEARNING DISORDER; MAGNOCELLULAR PATHWAY; MALE; MEMORY; MENTAL TASK; MILD COGNITIVE IMPAIRMENT; PARVOCELLULAR PATHWAY; PERCEPTIVE DISCRIMINATION; SCHIZOPHRENIA; STIMULUS RESPONSE; VISUAL NERVOUS SYSTEM;

ADULT; AGED; ANALYSIS OF VARIANCE; ASSOCIATION LEARNING; CASE-CONTROL STUDIES; DISCRIMINATION (PSYCHOLOGY); FEMALE; FUNCTIONAL LATERALITY; HIPPOCAMPUS; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; LINEAR MODELS; MAGNETIC RESONANCE IMAGING; MALE; MEMORY DISORDERS; MIDDLE AGED; MILD COGNITIVE IMPAIRMENT; NEUROPSYCHOLOGICAL TESTS; ORIENTATION; PHOTIC STIMULATION; SCHIZOPHRENIA; VISUAL PATHWAYS;

EID: 84868333553     PISSN: 00283932     EISSN: 18733514     Source Type: Journal    
DOI: 10.1016/j.neuropsychologia.2012.10.010     Document Type: Article

References (69)

1. Adriano F., Caltagirone C., Spalletta G. Hippocampal volume reduction in first-episode and chronic schizophrenia: a review and meta-analysis. Neuroscientist 2012, 18:180-200.
2. Armstrong K., Kose S., Williams L., Woolard A., Heckers S. Impaired associative inference in patients with schizophrenia. Schizophrenia Bulletin 2012, 38:622-629.
3. Atienza M., Atalaia-Silva K.C., Gonzalez-Escamilla G., Gil-Neciga E., Suarez-Gonzalez A., Cantero J.L. Associative memory deficits in mild cognitive impairment: the role of hippocampal formation. Neuroimage 2011, 57:1331-1342.
4. Bar M. A cortical mechanism for triggering top-down facilitation in visual object recognition. Journal of Cognitive Neuroscience 2003, 15:600-609.
5. Baxter M.G. Involvement of medial temporal lobe structures in memory and perception. Neuron 2009, 61:667-677.
6. Blackwell A.D., Sahakian B.J., Vesey R., Semple J.M., Robbins T.W., Hodges J.R. Detecting dementia: novel neuropsychological markers of preclinical Alzheimer's disease. Dementia and Geriatric Cognitive Disorders 2004, 17:42-48.
7. Braun M., Weinrich C., Finke C., Ostendorf F., Lehmann T.N., Ploner C.J. Lesions affecting the right hippocampal formation differentially impair short-term memory of spatial and nonspatial associations. Hippocampus 2011, 21:309-318.
8. Bussey T.J., Saksida L.M. Memory, perception, and the ventral visual-perirhinal-hippocampal stream: thinking outside of the boxes. Hippocampus 2007, 17:898-908.
9. Butler P.D., Martinez A., Foxe J.J., Kim D., Zemon V., Silipo G., et al. Subcortical visual dysfunction in schizophrenia drives secondary cortical impairments. Brain 2007, 130:417-430.
10. Butler P.D., Martinez A., Foxe J.J., Kim D., Zemon V., Silipo G., et al. Reply: a few remarks on assessing magnocellular sensitivity in schizophrenic patients. Brain 2007, 130:e84.
11. Butler P.D., Zemon V., Schechter I., Saperstein A.M., Hoptman M.J., Lim K.O., et al. Early-stage visual processing and cortical amplification deficits in schizophrenia. Archives of General Psychiatry 2005, 62:495-504.
12. Callaway E.M. Structure and function of parallel pathways in the primate early visual system. Journal of Physiology 2005, 566:13-19.
13. Chen Y., Levy D.L., Sheremata S., Nakayama K., Matthysse S., Holzman P.S. Effects of typical, atypical, and no antipsychotic drugs on visual contrast detection in schizophrenia. American Journal of Psychiatry 2003, 160:1795-1801.
14. de Haan E.H., Cowey A. On the usefulness of 'what' and 'where' pathways in vision. Trends in Cognitive Sciences 2011, 15:460-466.
15. de Rover M., Pironti V.A., McCabe J.A., Acosta-Cabronero J., Arana F.S., Morein-Zamir S., et al. Hippocampal dysfunction in patients with mild cognitive impairment: a functional neuroimaging study of a visuospatial paired associates learning task. Neuropsychologia 2011, 49:2060-2070.
16. Elvevag B., Egan M.F., Goldberg T.E. Paired-associate learning and memory interference in schizophrenia. Neuropsychologia 2000, 38:1565-1575.
17. Ferreira L.K., Diniz B.S., Forlenza O.V., Busatto G.F., Zanetti M.V. Neurostructural predictors of Alzheimer's disease: a meta-analysis of VBM studies. Neurobiology of Aging 2011, 32:1733-1741.
18. First M.B., Spitzer R.L., Gibbon M., Williams J.B.W. Structured clinical interview for DSM-IV axis I disorders, clinician version (SCID-CV). 1996, American Psychiatric Press, Washington, DC.
19. Fischl B., Salat D.H., van der Kouwe A.J., Makris N., Ségonne F., Quinn B.T., et al. Sequence-independent segmentation of magnetic resonance images. Neuroimage 2004, 23(1):S69-S84.
20. Folstein M.F., Folstein S.E., McHugh P.R. Mini-mental state. A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research 1975, 12:189-198.
21. Fouquet M., Desgranges B., La Joie R., Rivière D., Mangin J.F., Landeau B., et al. Role of hippocampal CA1 atrophy in memory encoding deficits in amnestic mild cognitive impairment. Neuroimage 2012, 59:3309-3315.
22. Goodbourn P.T., Bosten J.M., Hogg R.E., Bargary G., Lawrance-Owen A.J., Mollon J.D. Do different 'magnocellular tasks' probe the same neural substrate?. Philosophical Transaction of the Royal Society B: Biological Sciences 2012, 279:4263-4271.
23. Gronenschild E.H., Habets P., Jacobs H.I., Mengelers R., Rozendaal N., van Os J., et al. The effects of FreeSurfer version, workstation type, and Macintosh operating system version on anatomical volume and cortical thickness measurements. PLoS One 2012, 7:e38234.
24. Hanseeuw B., Dricot L., Kavec M., Grandin C., Seron X., Ivanoiu A. Associative encoding deficits in amnestic mild cognitive impairment: a volumetric and functional MRI study. Neuroimage 2011, 56:1743-1748.
25. Heckers S., Konradi C. Hippocampal pathology in schizophrenia. Current Topics in Behavioral Neuroscience 2010, 4:529-553.
26. Henke K. A model for memory systems based on processing modes rather than consciousness. Nature Reviews Neuroscience 2010, 11:523-532.
27. Iachini I., Iavarone A., Senese V.P., Ruotolo F., Ruggiero G. Visuospatial memory in healthy elderly, AD and MCI: a review. Current Aging Science 2009, 2:43-59.
28. Javitt D.C. When doors of perception close: bottom-up models of disrupted cognition in schizophrenia. Annual Review of Clinical Psychology 2009, 5:249-275.
29. Kéri S., Antal A., Szekeres G., Benedek G., Janka Z. Spatiotemporal visual processing in schizophrenia. Journal of Neuropsychiatry and Clinical Neurosciences 2002, 14:190-196.
30. Kéri S., Kiss I., Kelemen O., Benedek G., Janka Z. Anomalous visual experiences, negative symptoms, perceptual organization and the magnocellular pathway in schizophrenia: a shared construct?. Psychological Medicine 2005, 35:1445-1455.
31. Kesner R.P., Hopkins R.O. Mnemonic functions of the hippocampus: a comparison between animals and humans. Biological Psychology 2006, 73:3-18.
32. Kiss I., Fábián A., Benedek G., Kéri S. When doors of perception open: visual contrast sensitivity in never-medicated, first-episode schizophrenia. Journal of Abnormal Psychology 2010, 119:586-593.
33. Kühn S., Musso F., Mobascher A., Warbrick T., Winterer G., Gallinat J. Hippocampal subfields predict positive symptoms in schizophrenia: first evidence from brain morphometry. Translational Psychiatry 2012, 2:e127.
34. Lages M., Paul A. Visual long-term memory for spatial frequency?. Psychonomic Bulletin & Review 2006, 13:486-492.
35. Laprévote V., Oliva A., Delerue C., Thomas P., Boucart M. Patients with schizophrenia are biased toward low spatial frequency to decode facial expression at a glance. Neuropsychologia 2010, 48:4164-4168.
36. Lee A.C., Yeung L.K., Barense M.D. The hippocampus and visual perception. Frontiers in Human Neuroscience 2012, 6:91.
37. Lemos R., Figueiredo P., Santana I., Simões M.R., Castelo-Branco M. Temporal integration of 3D coherent motion cues defining visual objects of unknown orientation is impaired in amnestic mild cognitive impairment and Alzheimer's disease. Journal of Alzheimer's Disease 2012, 28:885-896.
38. Levy-Gigi E., Kelemen O., Gluck M.A., Kéri S. Impaired context reversal learning, but not cue reversal learning, in patients with amnestic mild cognitive impairment. Neuropsychologia 2011, 49:3320-3326.
39. Magnussen S., Greenlee M.W., Aslaksen P.M., Kildebo O.O. High-fidelity perceptual long-term memory revisited-and confirmed. Psychological Science 2003, 14:74-76.
40. Manelis A., Reder L.M., Hanson S.J. Dynamic changes in the medial temporal lobe during incidental learning of object-location associations. Cerebral Cortex 2012, 22:828-837.
41. Martínez A., Hillyard S.A., Dias E.C., Hagler D.J., Butler P.D., Guilfoyle D.N., et al. Magnocellular pathway impairment in schizophrenia: evidence from functional magnetic resonance imaging. Journal of Neuroscience 2008, 28:7492-7500.
42. Mueller S.G., Schuff N., Yaffe K., Madison C., Miller B., Weiner M.W. Hippocampal atrophy patterns in mild cognitive impairment and Alzheimer's disease. Human Brain Mapping 2010, 31:1339-1347.
43. Nassi J.J., Callaway E.M. Parallel processing strategies of the primate visual system. Nature Reviews Neuroscience 2009, 10:360-372.
44. Nickl-Jockschat T., Kleiman A., Schulz J.B., Schneider F., Laird A.R., Fox P.T., et al. Neuroanatomic changes and their association with cognitive decline in mild cognitive impairment: a meta-analysis. Brain Structure and Function 2012, 217:115-125.
45. Ongür D., Cullen T.J., Wolf D.H., Rohan M., Barreira P., Zalesak M., et al. The neural basis of relational memory deficits in schizophrenia. Archives of General Psychiatry 2006, 63:356-565.
46. Overall J.E., Gorham D.R. The brief psychiatric rating scale. Psychological Reports 1962, 10:799-812.
47. Petersen R.C., Smith G.E., Waring S.C., Ivnik R.J., Tangalos E.G., Kokmen E. Mild cognitive impairment: clinical characterization and outcome. Archives of Neurology 1999, 56:303-308.
48. Piekema C., Kessels R.P., Mars R.B., Petersson K.M., Fernández G. The right hippocampus participates in short-term memory maintenance of object-location associations. Neuroimage 2006, 33:374-382.
49. Reichenberg A., Harvey P.D. Neuropsychological impairments in schizophrenia: integration of performance-based and brain imaging findings. Psychological Bulletin 2007, 133:833-858.
50. Sahakian B.J., Morris R.G., Evenden J.L., Heald A., Levy R., Philpot M., et al. A comparative study of visuospatial memory and learning in Alzheimer-type dementia and Parkinson's disease. Brain 1988, 111:695-718.
51. Saksida L.M., Bussey T.J. The representational-hierarchical view of amnesia: translation from animal to human. Neuropsychologia 2010, 48:2370-2384.
52. Schobel S.A., Lewandowski N.M., Corcoran C.M., Moore H., Brown T., Malaspina D., et al. Differential targeting of the CA1 subfield of the hippocampal formation by schizophrenia and related psychotic disorders. Archives of General Psychiatry 2009, 66:938-946.
53. Segonne F., Dale A.M., Busa E., Glessner M., Salat D., Hahn H.K., et al. A hybrid approach to the skull stripping problem in MRI. Neuroimage 2004, 22:1060-1075.
54. Sehatpour P., Dias E.C., Butler P.D., Revheim N., Guilfoyle D.N., Foxe J.J., et al. Impaired visual object processing across an occipital-frontal-hippocampal brain network in schizophrenia: an integrated neuroimaging study. Archives of General Psychiatry 2010, 67:772-782.
55. Sincich L.C., Horton J.C. The circuitry of V1 and V2: integration of color, form, and motion. Annual Review of Neuroscience 2005, 28:303-326.
56. Singh V.V., Stojanoski B., Le A., Niemeier M. Spatial frequency-specific effects on the attentional bias: evidence for two attentional systems. Cortex 2011, 47:547-556.
57. Skottun B.C., Skoyles J. A few remarks on assessing magnocellular sensitivity in schizophrenic patients. Brain 2007, 130:e83.
58. Small S.A., Schobel S.A., Buxton R.B., Witter M.P., Barnes C.A. A pathophysiological framework of hippocampal dysfunction in ageing and disease. Nature Reviews Neuroscience 2011, 12:585-601.
59. Sowden P.T., Schyns P.G. Channel surfing in the visual brain. Trends in Cognitive Sciences 2006, 10:538-545.
60. Steen R.G., Mull C., McClure R., Hamer R.M., Lieberman J.A. Brain volume in first-episode schizophrenia: systematic review and meta-analysis of magnetic resonance imaging studies. British Journal of Psychiatry 2006, 188:510-518.
61. Stone W.S., His X. Declarative memory deficits and schizophrenia: problems and prospects. Neurobiology of Learning and Memory 2011, 96:544-552.
62. Suzuki W.A. Perception and the medial temporal lobe: evaluating the current evidence. Neuron 2009, 61:657-666.
63. Talpos J.C., Winters B.D., Dias R., Saksida L.M., Bussey T.J. A novel touchscreen-automated paired-associate learning (PAL) task sensitive to pharmacological manipulation of the hippocampus: a translational rodent model of cognitive impairments in neurodegenerative disease. Psychopharmacology (Berlin) 2009, 205:157-168.
64. Tamminga C.A., Stan A.D., Wagner A.D. The hippocampal formation in schizophrenia. American Journal of Psychiatry 2010, 167:1178-1193.
65. Thome A., Erickson C.A., Lipa P., Barnes C.A. Differential effects of experience on tuning properties of macaque MTL neurons in a passive viewing task. Hippocampus 2012, 22:2000-2111.
66. Van Essen D.C., Gallant J.L. Neural mechanisms of form and motion processing in the primate visual system. Neuron 1994, 13:1-10.
67. van Strien N.M., Widerøe M., van de Berg W.D., Uylings H.B. Imaging hippocampal subregions with in vivo MRI: advances and limitations. Nature Reviews Neuroscience 2011, 13:70.
68. Woods S.W. Chlorpromazine equivalent doses for the newer atypical antipsychotics. Journal of Clinical Psychiatry 2003, 64:663-667.
69. Yoon J., Seo Y., Kim J., Lee I. Hippocampus is required for paired associate memory with neither delay nor trial uniqueness. Learning and Memory 2011, 19:1-8.