Magnocellular contributions to impaired motion processing in schizophrenia

Schizophrenia Research

Volumn 82, Issue 1, 2006, Pages 1-8

  Kim, Dongsoo ^a   Wylie, Glenn ^a   Pasternak, Roey ^a   Butler, Pamela D ^a,b   Javitt, Daniel C ^a,b  

^a NATHAN S KLINE INSTITUTE FOR PSYCHIATRIC RESEARCH   (United States)

^b NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Magnocellular; Motion; NMDA; Schizophrenia; Visual

Indexed keywords

ADULT; ARTICLE; BEHAVIOR; CLINICAL ARTICLE; COGNITIVE DEFECT; CONTROLLED STUDY; CORRELATION ANALYSIS; EVOKED VISUAL RESPONSE; FEMALE; HUMAN; LUMINANCE; MALE; MOTION; NEUROPHYSIOLOGY; PERFORMANCE; PRIORITY JOURNAL; SCHIZOPHRENIA; STATISTICAL SIGNIFICANCE; STEADY STATE; VELOCITY; VISION; VISUAL SYSTEM;

ADULT; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; EVOKED POTENTIALS, VISUAL; FEMALE; HUMANS; MALE; MOTION PERCEPTION; PERCEPTUAL DISORDERS; SCHIZOPHRENIA; VISION, BINOCULAR; VISUAL FIELDS; VISUAL PATHWAYS; VISUAL PERCEPTION;

EID: 32044468948     PISSN: 09209964     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.schres.2005.10.008     Document Type: Article

References (41)

1. W.M. Abi-Saab, D.C. D'Souza, B. Moghaddam, and J.H. Krystal The NMDA antagonist model for schizophrenia: promise and pitfalls Pharmacopsychiatry 31 Suppl 2 1998 104 109
2. J.W. Bisley, and T. Pasternak The multiple roles of visual cortical areas MT/MST in remembering the direction of visual motion Cereb. Cortex 10 2000 1053 1065
3. D.F. Braus, W. Weber-Fahr, H. Tost, M. Ruf, and F.A. Henn Sensory information processing in neuroleptic-naive first-episode schizophrenic patients: a functional magnetic resonance imaging study Arch. Gen. Psychiatry 59 2002 696 701
4. C.A. Brenner, M.A. Wilt, P.H. Lysaker, A. Koyfman, and B.F. O'Donnell Psychometrically matched visual-processing tasks in schizophrenia spectrum disorders J. Abnorm. Psychology 112 2003 28 37
5. P.D. Butler, I. Schechter, V. Zemon, S.G. Schwartz, V.C. Greenstein, J. Gordon, C.E. Schroeder, and D.C. Javitt Dysfunction of early stage visual processing in schizophrenia Am. J. Psychiatry 158 2001 1126 1133
6. P.D. Butler, L.A. DeSanti, J. Maddox, J.M. Harkavy-Friedman, X.F. Amador, R.R. Goetz, D.C. Javitt, and J.M. Gorman Visual backward-masking deficits in schizophrenia: relationship to visual pathway function and symptomatology Schizophr. Res. 59 2003 199 209
7. P.D. Butler, V. Zemon, I. Schechter, A.M. Saperstein, M.J. Hoptman, K.O. Lim, N. Revheim, G. Silipo, and D.C. Javitt Early-stage visual processing and cortical amplification deficits in schizophrenia Arch. Gen. Psychiatry 62 2005 495 504
8. C. Chapman, R. Hoag, and D. Giaschi The effect of disrupting the human magnocellular pathway on global motion perception Vis. Res. 44 2004 2551 2557
9. Y. Chen, G.P. Palafox, K. Nakayama, D.L. Levy, S. Matthysse, and P.S. Holzman Motion perception in schizophrenia Arch. Gen. Psychiatry 56 1999 149 154
10. Y. Chen, K. Nakayama, D. Levy, S. Matthysse, and P. Holzman Processing of global, but not local, motion direction is deficient in schizophrenia Schizophr. Res. 61 2003 215 227
11. Y. Chen, D.L. Levy, S. Sheremata, and P.S. Holzman Compromised late-stage motion processing in schizophrenia Biol. Psychiatry 55 2004 834 841
12. Y. Chen, L.C. Bidwell, and P.S. Holzman Visual motion integration in schizophrenia patients, their first-degree relatives, and patients with bipolar disorder Schizophr. Res. 74 2005 271 281
13. J.T. Coyle The glutamatergic dysfunction hypothesis for schizophrenia Harv. Rev. Psychiatry 3 1996 241 253
14. D.J. Felleman, and D.C. Van Essen Distributed hierarchical processing in the primate cerebral cortex Cereb. Cortex 1 1991 1 47
15. J.J. Foxe, G.M. Doniger, and D.C. Javitt Early visual processing deficits in schizophrenia: impaired P1 generation revealed by high-density electrical mapping NeuroReport 12 2001 3815 3820
16. P. Heggelund, and E. Hartveit Neurotransmitter receptors mediating excitatory input to cells in the cat lateral geniculate nucleus. I. Lagged cells J. Neurophysiol. 63 1990 1347 1360
17. A.B. Hollingshead, and F.L. Redlich Social Class and Mental Illness 1958 Wiley New York
18. A.L. Humphrey, and R.E. Weller Functionally distinct groups of X-cells in the lateral geniculate nucleus of the cat J. Comp. Neurol. 268 1988 429 447
19. A.L. Humphrey, A.B. Saul, and J.C. Feidler Strobe rearing prevents the convergence of inputs with different response timings onto area 17 simple cells J. Neurophysiol. 80 1998 3005 3020
20. D.C. Javitt, and S.R. Zukin Recent advances in the phencyclidine model of schizophrenia Am. J. Psychiatry 148 1991 1301 1308
21. S. Keri, O. Kelemen, G. Benedek, and Z. Janka Vernier threshold in patients with schizophrenia and in their unaffected siblings Neuropsychology 18 2004 537 542
22. D. Kim, V. Zemon, A. Saperstein, P.D. Butler, and D.C. Javitt Dysfunction of early stage visual processing in schizophrenia: harmonic analysis Schizophr. Res. 76 2005 55 65
23. Y.H. Kwon, M. Esguerra, and M. Sur NMDA and non-NMDA receptors mediate visual responses of neurons in the cat's lateral geniculate nucleus J. Neurophysiol. 66 1991 414 428
24. Y.H. Kwon, S.B. Nelson, L.J. Toth, and M. Sur Effect of stimulus contrast and size on NMDA receptor activity in cat lateral geniculate nucleus J. Neurophysiol. 68 1992 182 196
25. K. Lam, Y. Kaneoke, A. Gunji, H. Yamasaki, E. Matsumoto, T. Naito, and R. Kakigi Magnetic response of human extrastriate cortex in the detection of coherent and incoherent motion Neuroscience 97 2000 1 10
26. C.S. Li Impaired detection of visual motion in schizophrenia patients Prog. Neuro-psychopharmacol. Biol. Psychiatry 26 2002 929 934
27. D.J. McKeefry, J.D. Watson, R.S. Frackowiak, K. Fong, and S. Zeki The activity in human areas V1/V2, V3, and V5 during the perception of coherent and incoherent motion NeuroImage 5 1997 1 12
28. J.W. Newcomer, N.B. Farber, V. Jevtovic-Todorovic, G. Selke, A.K. Melson, T. Hershey, S. Craft, and J.W. Olney Ketamine-induced NMDA receptor hypofunction as a model of memory impairment and psychosis Neuropsychopharmacology 20 1999 106 118
29. B.F. O'Donnell, J.M. Swearer, L.T. Smith, P.G. Nestor, M.E. Shenton, and R.W. McCarley Selective deficits in visual perception and recognition in schizophrenia Am. J. Psychiatry 153 1996 687 692
30. G.A. Orban, D. Van Essen, and W. Vanduffel Comparative mapping of higher visual areas in monkeys and humans Trends Cogn. Sci. 8 2004 315 324
31. F.H. Previc, M. Liotti, C. Blakemore, J. Beer, and P. Fox Functional imaging of brain areas involved in the processing of coherent and incoherent wide field-of-view visual motion Exp. Brain Res. 131 2000 393 405
32. G. Rees, K. Friston, and C. Koch A direct quantitative relationship between the functional properties of human and macaque V5 Nat. Neurosci. 3 2000 716 723
33. C. Rivadulla, J. Sharma, and M. Sur Specific roles of NMDA and AMPA receptors in direction-selective and spatial phase-selective responses in visual cortex J. Neurosci. 21 2001 1710 1719
34. J. Ross, D.R. Badcock, and A. Hayes Coherent global motion in the absence of coherent velocity signals Curr. Biol. 10 2000 679 682
35. I. Schechter, P.D. Butler, G. Silipo, V. Zemon, and D.C. Javitt Magnocellular and parvocellular contributions to backward masking dysfunction in schizophrenia Schizophr. Res. 64 2003 91 101
36. B.D. Schwartz, B.A. Maron, W.J. Evans, and D.K. Winstead High velocity transient visual processing deficits diminish ability of patients with schizophrenia to recognize objects Neuropsychiatry Neuropsychol. Behav. Neurol. 12 1999 170 177
37. W.L. Slaghuis Contrast sensitivity for stationary and drifting spatial frequency gratings in positive- and negative-symptom schizophrenia J. Abnorm. Psychology 107 1998 49 62
38. W.L. Slaghuis Spatio-temporal luminance contrast sensitivity and visual backward masking in schizophrenia Exp. Brain Res. 156 2004 196 211
39. A. Thiele, K.R. Dobkins, and T.D. Albright Neural correlates of chromatic motion perception Neuron 32 2001 351 358
40. I. Ulbert, G. Karmos, G. Heit, and E. Halgren Early discrimination of coherent versus incoherent motion by multiunit and synaptic activity in human putative MT+ Hum. Brain Mapp. 13 2001 226 238
41. S.M. Zeki Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey J. Physiol. 236 1974 549 573