Spatial homogeneity and task-synchrony of the trial-related hemodynamic signal

NeuroImage

Volumn 59, Issue 3, 2012, Pages 2783-2797

  Sirotin, Yevgeniy B ^a   Cardoso, Mariana ^b   Lima, Bruss ^b   Das, Aniruddha ^b  

^a ROCKEFELLER UNIVERSITY   (United States)

^b Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ANALYTICAL PARAMETERS; ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ARTICLE; BRAIN ELECTROPHYSIOLOGY; CONTROLLED STUDY; FUNCTIONAL MAGNETIC RESONANCE IMAGING; FUNCTIONAL NEUROIMAGING; HAPLORHINI; HEMODYNAMICS; IMAGE PROCESSING; NONHUMAN; OSCILLATION; PRIORITY JOURNAL; SIGNAL PROCESSING; SPATIAL HOMOGENEITY; STIMULUS RESPONSE; TASK PERFORMANCE; VISUAL STIMULATION;

ALGORITHMS; ANIMALS; BLOOD VOLUME; CEREBROVASCULAR CIRCULATION; ELECTRODES; ELECTROPHYSIOLOGICAL PHENOMENA; EVOKED POTENTIALS, VISUAL; FIXATION, OCULAR; HEMODYNAMICS; IMAGE PROCESSING, COMPUTER-ASSISTED; MACACA MULATTA; MAGNETIC RESONANCE IMAGING; PHOTIC STIMULATION; PSYCHOMOTOR PERFORMANCE;

EID: 84855439209     PISSN: 10538119     EISSN: 10959572     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2011.10.019     Document Type: Article

References (52)

1. Arieli A., Grinvald A., Slovin H. Dural substitute for long-term imaging of cortical activity in behaving monkeys and its clinical implications. J. Neurosci. Methods 2002, 114:119-133.
2. Attwell D., Iadecola C. The neural basis of functional brain imaging signals. Trends Neurosci 2002, 25(12):621-625.
3. Bonhoeffer T., Grinvald A. Optical imaging based on intrinsic signals: the methodology. Brain Mapping: The Methods 1996, Academic Press, San Diego. A.W. Toga, J.C. Mazziotta (Eds.).
4. Boorman L., Kennerley A.J., Johnston D., Jones M., Zheng Y., Redgrave P., Berwick J. Negative blood oxygen level dependence in the rat: a model for investigating the role of suppression in neurovascular coupling. J. Neurosci. 2010, 30(12):4285-4294.
5. Das A., Gilbert C.D. Long-range horizontal connections and their role in cortical reorganization revealed by optical recording of cat primary visual cortex. Nature 1995, 375:780-784.
6. Das A., Sirotin Y.B. What could underlie the trial-related signal? A response to the commentaries by Drs. Kleinschmidt and Muller, and Drs. Handwerker and Bandettini. Neuroimage 2011, 55:1413-1418.
7. Devor A., Dunn A.K., Andermann M.L., Ulbert I., Boas D.A., Dale A.M. Coupling of total hemoglobin concentration, oxygenation and neural activity in rat somatosensory cortex. Neuron 2003, 39:353-359.
8. Devor A., Tian P., Nishimura N., Teng I.C., Hillman E.M.C., Narayanan S.N., Ulbert I., Boas D.A., Kleinfeld D., Dale A.M. Suppressed neuronal activity and concurrent arteriolar vasoconstriction may explain negative blood oxygenation level-dependent signal. J. Neurosci. 2007, 27(16):4452-4459.
9. Donner T.H., Sagi D., Bonneh Y.S., Heeger D.J. Opposite neural signatures of motion-induced blindness in human dorsal and ventral visual cortex. J. Neurosci. 2008, 28(41):10298-10310.
10. Fox M.D., Snyder A.Z., Zacks J.M., Raichle M.E. Coherent spontaneous activity accounts for trial-to-trial variability in human evoked brain responses. Nat. Neurosci. 2006, 9(1):23-25.
11. Fukuda M., Moon C.-H., Wang P., Kim S.-G. Mapping iso-orientation columns by contrast agent-enhanced functional magnetic resonance imaging: reproducibility, specificity, and evaluation by optical imaging of intrinsic signal. J. Neurosci. 2006, 26(46):11821-11832.
12. Hamel E. Cholinergic modulation of the cortical microvascular bed. Prog. Brain Res. 2004, 145:171-178.
13. Heeger D.J., Huk A.C., Geisler W.S., Albrecht D.G. Spikes versus BOLD: what does neuroimaging tell us about neuronal activity?. Nat. Neurosci. 2000, 3:631-633.
14. Heinemann L., Kleinschmidt A., Muller N.G. Exploring BOLD changes during spatial attention in non-stimulated visual cortex. PLoS One 2009, 4(5):e5560.
15. Hopf J.-M., Boehler C.N., Luck S.J., Tsotsos J.K., Heinze H.-J., Schoenfeld M.A. Direct neurophysiological evidence for spatial suppression surrounding the focus of attention in vision. Proc. Natl. Acad. Sci. U.S.A. 2006, 103(4):1053-1058.
16. Hopf J.-M., Luck S.J., Boelmans K., Schoenfeld M.A., Boehler C.N., Rieger J., Heinze H.-J. The neural site of attention matches the spatial scale of perception. J. Neurosci. 2006, 26(13):3532-3540.
17. Iacovella, V., Hasson, U., in press. The relationship between BOLD signal and autonomic nervous system functions: implications for processing of "physiological noise". Magn. Reson. Imaging, Article in press (e-Pub on line).
18. Iadecola C., Nedergaard M. Glial regulation of the cerebral microvasculature. Nat. Neurosci. 2007, 10(11):1369-1376.
19. Jack A.I., Shulman G.L., Snyder A.Z., McAvoy M.P., Corbetta M. Separate modulations of human V1 associated with spatial attention and task structure. Neuron 2006, 51:135-147.
20. Kalatsky V.A., Stryker M.P. New paradigm for optical imaging: temporally encoded maps of intrinsic signals. Neuron 2003, 38:529-545.
21. Kastner S., Pinsk M.A., DeWeerd P., Desimone R., Ungerleider L.G. Increased activity in human visual cortex during directed attention in the absence of visual stimulation. Neuron 1999, 22:751-761.
22. Kleinschmidt A., Muller N.G. The blind, the lame, and the poor signals of brain function-a comment on Sirotin and Das (2009). Neuroimage 2010, 50(2):622-625.
23. Krimer L.S., Muly E.C., Williams G.V., Goldman-Rakic P.S. Dopaminergic regulation of cerebral cortical microcirculation. Nat. Neurosci. 1998, 1(4):286-289.
24. Logothetis N.K. What we can and what we cannot do with fMRI. Nature 2008, 453:869-878.
25. Logothetis N.K., Pauls J., Augath M., Trinath T., Oeltermann A. Neurophysiological investigation of the basis of the fMRI signal. Nature 2001, 412:150-157.
26. Logothetis N.K., Wandell B.A. Interpreting the BOLD signal. Annu. Rev. Physiol. 2004, 66:735-769.
27. Lucas B.D., Kanade T. An iterative image registration technique with an application to stereo vision (IJCAI). Proceedings of the 7th International Joint Conference on Artificial Intelligence IJCAI 1981, 81:674-679.
28. Mathiesen C., Caesar K., Akgoren N., Lauritzen M. Modification of activity-dependent increases in cerebral blood flow by excitatory synaptic activity and spikes in rat cerebellar cortex. J. Physiol. 1998, 512(2):555-566.
29. Matsuda K., Nagami T., Kawano K., Yamane S. A new system for measuring eye position on a personal computer 2000, 744.2.
30. Mayhew J.E.W., Askew S., Zheng Y., Porrill J., Westby G.W.M., Redgrave P., Rector D.M., Harper R.M. Cerebral vasomotion: a 0.1-Hz oscillation in reflected light imaging of neural activity. Neuroimage 1996, 4:183-193.
31. Mayhew J.E.W., Zheng Y., Hou Y., Vuksanovic B., Berwick J., Askew S., Coffey P. Spectroscopic analysis of changes in remitted illumination: the response to increased neural activity in brain. Neuroimage 1999, 10:304-326.
32. Moradi F., Hipp C., Koch C. Activity in the visual cortex is modulated by top-down attention locked to reaction time. J. Cogn. Neurosci. 2007, 19(2):331-340.
33. Muller N.G., Kleinschmidt A. The attentional 'spotlight's' penumbra: center-surround modulation in striate cortex. Neuroreport 2004, 15:977-980.
34. Muller N.G., Mollenhauer M., Rosler A., Kleinschmidt A. The attentional field has a Mexican hat distribution. Vision Res. 2005, 45(9):1129-1137.
35. Nemoto M., Sheth S.A., Guiou M.W., Pouratian N., Chen J.W., Toga A.W. Functional signal- and paradigm-dependent linear relationships between synaptic activity and hemodynamic responses in rat somatosensory cortex. J. Neurosci. 2004, 24(15):3850-3861.
36. Prahl S. Tabulated molar extinction coefficient for hemoglobin in water http://omlc%20ogi%20edu/spectra/hemoglobin/summary%20html.
37. Raichle M.E., Mintun M.A. Brain work and brain imaging. Annu. Rev. Neurosci. 2006, 29:449-476.
38. Ratzlaff E.H., Grinvald A. A tandem-lens epifluorescence macroscope: hundred-fold brightness advantage for wide-field imaging. J. Neurosci. Methods 1991, 36:127-137.
39. Rees G., Friston K.J., Koch C. A direct quantitative relationship between the functional properties of human and macaque V5. Nat. Neurosci. 2000, 3(7):716-723.
40. Ress D., Backus B.T., Heeger D.J. Activity in primary visual cortex predicts performance in a visual detection task. Nat. Neurosci. 2000, 3(9):940-945.
41. Ruff C.C., Driver J. Attentional preparation for a lateralized visual distractor: behavioral and fMRI evidence. J. Cogn. Neurosci. 2006, 18(4):522-538.
42. Serences J.T., Yantis S., Culberson A., Awh E. Preparatory activity in visual cortex indexes distractor suppression during covert spatial orienting. J. Neurophysiol. 2004, 92:3538-3545.
43. Sheth S.A., Nemoto M., Guiou M., Walker M.A., Pouratian N., Hageman N., Toga A.W. Linear and nonlinear relationships between neuronal activity, oxygen metabolism and hemodynamic responses. Neuron 2004, 42:347-355.
44. Shmuel A., Augath M., Oeltermann A., Logothetis N.K. Negative functional MRI response correlates with decreases in neuronal activity in monkey visual area V1. Nat. Neurosci. 2006, 9(4):569-577.
45. Shtoyerman E., Arieli A., Slovin H., Vanzetta I., Grinvald A. Long-term optical imaging and spectroscopy reveal mechanisms underlying the intrinsic signal and stability of cortical maps in V1 of behaving monkeys. J. Neurosci. 2000, 20(21):8111-8121.
46. Silver M.A., Ress D., Heeger D.J. Neural correlates of sustained spatial attention in human early visual cortex. J. Neurophysiol. 2007, 97:229-237.
47. Sirotin Y.B., Das A. Anticipatory haemodynamic signals in sensory cortex not predicted by local neuronal activity. Nature 2009, 457:475-479.
48. Sirotin Y.B., Hillman E.M.C., Bordier C., Das A. Spatiotemporal precision and hemodynamic mechanism of optical point-spreads in alert primates. Proc. Natl. Acad. Sci. U.S.A. 2009, 106(43):18390-18395.
49. Slotnick S.D., Hopfinger J.B., Klein S.A., Sutter E.E. Darkness beyond the light: attentional inhibition surrounding the classic spotlight. Neuroreport 2002, 13(6):773-778.
50. Smith A.T., Singh K.D., Greenlee M.W. Attentional suppression of activity in the human visual cortex. Neuroreport 2000, 11(2):271-278.
51. Sylvester C.M., Jack A.I., Corbetta M., Shulman G.L. Anticipatory suppression of nonattended locations in visual cortex marks target location and predicts perception. J. Neurosci. 2008, 28(26):6549-6556.
52. Sylvester C.M., Shulman G.L., Jack A.I., Corbetta M. Asymmetry of anticipatory activity in visual cortex predicts the locus of attention and perception. J. Neurosci. 2007, 27(52):14424-14433.