Dependence of BOLD signal change on tactile stimulus intensity in SI of primates

Magnetic Resonance Imaging

Volumn 25, Issue 6, 2007, Pages 784-794

  Zhang, Na ^a,b   Gore, John C ^a,b,c,d   Chen, Li M ^a,b   Avison, Malcolm J ^a,b  

^a VANDERBILT UNIVERSITY   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c VANDERBILT UNIVERSITY   (United States)

^d VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Digits; fMRI; Gamma variate; Linearity; Somatosensory cortex; Stimulus intensity

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; BRAIN MAPPING; BRAIN REGION; ELECTROPHYSIOLOGY; FUNCTIONAL MAGNETIC RESONANCE IMAGING; NERVE POTENTIAL; NEUROANATOMY; NONHUMAN; PRIMATE; PRIORITY JOURNAL; SIGNAL PROCESSING; SOMATOSENSORY CORTEX; SQUIRREL MONKEY; TACTILE STIMULATION; TOPOGRAPHY;

ALGORITHMS; ANIMALS; BRAIN MAPPING; ELECTROPHYSIOLOGY; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MODELS, STATISTICAL; PRIMATES; SAIMIRI; TIME FACTORS; TOUCH;

PRIMATES;

EID: 34447567164     PISSN: 0730725X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mri.2007.05.002     Document Type: Article

References (62)

1. Yacoub E., and Hu X. Detection of the early decrease in fMRI signal in the motor area. Magn Reson Med 45 2 (2001) 184-190
2. Stippich C., et al. Motor, somatosensory and auditory cortex localization by fMRI and MEG. Neuroreport 9 9 (1998) 1953-1957
3. Li Hegner Y., et al. BOLD adaptation in vibrotactile stimulation: neuronal networks involved in frequency discrimination. J Neurophysiol 97 1 (2007) 264-271
4. Masamoto K., et al. Relationship between neural, vascular, and BOLD signals in isoflurane-anesthetized rat somatosensory cortex. Cereb Cortex 17 4 (2007) 942-950
5. Van Camp N., Verhoye M., and Van der Linden A. Stimulation of the rat somatosensory cortex at different frequencies and pulse widths. NMR Biomed 19 1 (2006) 10-17
6. Zhu X.H., et al. Simultaneous oxygenation and perfusion imaging study of functional activity in primary visual cortex at different visual stimulation frequency: quantitative correlation between BOLD and CBF changes. Magn Reson Med 40 5 (1998) 703-711
7. Vanduffel W., et al. Visual motion processing investigated using contrast agent-enhanced fMRI in awake behaving monkeys. Neuron 32 4 (2001) 565-577
8. Nagaoka T., et al. Increases in oxygen consumption without cerebral blood volume change during visual stimulation under hypotension condition. J Cereb Blood Flow Metab 26 8 (2006) 1043-1051
9. Logothetis N.K., et al. Functional imaging of the monkey brain. Nat Neurosci 2 6 (1999) 555-562
10. Duong T.Q., et al. Spatiotemporal dynamics of the BOLD fMRI signals: toward mapping submillimeter cortical columns using the early negative response. Magn Reson Med 44 2 (2000) 231-242
11. Hamzei F., et al. Reduction of excitability ("inhibition") in the ipsilateral primary motor cortex is mirrored by fMRI signal decreases. Neuroimage 17 1 (2002) 490-496
12. Buxton R.B., et al. Modeling the hemodynamic response to brain activation. Neuroimage 23 Suppl 1 (2004) S220-S233
13. Wu G., et al. Transient relationships among BOLD, CBV, and CBF changes in rat brain as detected by functional MRI. Magn Reson Med 48 6 (2002) 987-993
14. Hyder F., et al. Quantitative functional imaging of the brain: towards mapping neuronal activity by BOLD fMRI. NMR Biomed 14 7-8 (2001) 413-431
15. Ogawa S., et al. Functional brain mapping by blood oxygenation level-dependent contrast magnetic resonance imaging. A comparison of signal characteristics with a biophysical model. Biophys J 64 3 (1993) 803-812
16. Ogawa S., Lee T.M., and Barrere B. The sensitivity of magnetic resonance image signals of a rat brain to changes in the cerebral venous blood oxygenation. Magn Reson Med 29 2 (1993) 205-210
17. Chen L.M., et al. Fine fingerpad topography in squirrel monkey SII cortex revealed by high field fMRI. Soc. Neurosci. Abstr. (2006) 212.2
18. Chen L.M., Friedman R.M., and Roe A.W. Optical imaging of a tactile illusion in area 3b of the primary somatosensory cortex. Science 302 5646 (2003) 881-885
19. Chen L.M., et al. Fine-scale organization of SI (area 3b) in the squirrel monkey revealed with intrinsic optical imaging. J Neurophysiol 86 6 (2001) 3011-3029
20. Tang L., Avison M.J., and Gore C.J. Non-linear BOLD responses for transient deactivations in V1. Proceedings of the 2006 Scientific Sessions of ISMRM (14th), Seattle, WA (2006)
21. Vazquez A.L., and Noll D.C. Nonlinear aspects of the BOLD response in functional MRI. Neuroimage 7 2 (1998) 108-118
22. Mohamed F.B., et al. BOLD fMRI of the visual cortex: quantitative responses measured with a graded stimulus at 1.5 Tesla. J Magn Reson Imaging 16 2 (2002) 128-136
23. Rainer G., et al. Nonmonotonic noise tuning of BOLD fMRI signal to natural images in the visual cortex of the anesthetized monkey. Curr Biol 11 11 (2001) 846-854
24. Robson M.D., Dorosz J.L., and Gore J.C. Measurements of the temporal fMRI response of the human auditory cortex to trains of tones. Neuroimage 7 3 (1998) 185-198
25. Krause T., et al. Representational overlap of adjacent fingers in multiple areas of human primary somatosensory cortex depends on electrical stimulus intensity: an fMRI study. Brain Res 899 1-2 (2001) 36-46
26. Wandell B.A. Computational neuroimaging of human visual cortex. Annu Rev Neurosci 22 (1999) 145-173
27. Birn R.M., and Bandettini P.A. The effect of stimulus duty cycle and "off" duration on BOLD response linearity. Neuroimage 27 1 (2005) 70-82
28. Logothetis N.K., and Wandell B.A. Interpreting the BOLD signal. Annu Rev Physiol 66 (2004) 735-769
29. Nemoto M., et al. Functional signal- and paradigm-dependent linear relationships between synaptic activity and hemodynamic responses in rat somatosensory cortex. J Neurosci 24 15 (2004) 3850-3861
30. Sheth S., et al. Evaluation of coupling between optical intrinsic signals and neuronal activity in rat somatosensory cortex. Neuroimage 19 3 (2003) 884-894
31. 2*-weighted MR images during somatosensory stimulation of rat. Magn Reson Med 41 3 (1999) 469-473
32. Mathiesen C., et al. Modification of activity-dependent increases of cerebral blood flow by excitatory synaptic activity and spikes in rat cerebellar cortex. J Physiol 512 Pt 2 (1998) 555-566
33. Ogawa S., et al. An approach to probe some neural systems interaction by functional MRI at neural time scale down to milliseconds. Proc Natl Acad Sci U S A 97 20 (2000) 11026-11031
34. Rees G., Friston K., and Koch C. A direct quantitative relationship between the functional properties of human and macaque V5. Nat Neurosci 3 7 (2000) 716-723
35. Sur M., Nelson R.J., and Kaas J.H. Representations of the body surface in cortical areas 3b and 1 of squirrel monkeys: comparisons with other primates. J Comp Neurol 211 2 (1982) 177-192
36. Sur M., Garraghty P.E., and Bruce C.J. Somatosensory cortex in macaque monkeys: laminar differences in receptive field size in areas 3b and 1. Brain Res 342 2 (1985) 391-395
37. Kaas J.H. What, if anything, is SI? Organization of first somatosensory area of cortex. Physiol Rev 63 1 (1983) 206-231
38. Weber R., et al. A fully noninvasive and robust experimental protocol for longitudinal fMRI studies in the rat. Neuroimage 29 4 (2006) 1303-1310
39. Suh M., et al. Blood volume and hemoglobin oxygenation response following electrical stimulation of human cortex. Neuroimage 31 1 (2006) 66-75
40. Ferretti A., et al. Cortical brain responses during passive nonpainful median nerve stimulation at low frequencies (0.5-4 Hz): an fMRI study. Hum Brain Mapp 28 7 (2006) 645-653
41. Yang X., Hyder F., and Shulman R.G. Functional MRI BOLD signal coincides with electrical activity in the rat whisker barrels. Magn Reson Med 38 6 (1997) 874-877
42. Silva A.C., et al. Simultaneous blood oxygenation level-dependent and cerebral blood flow functional magnetic resonance imaging during forepaw stimulation in the rat. J Cereb Blood Flow Metab 19 8 (1999) 871-879
43. Singh M., Kim S., and Kim T.S. Correlation between BOLD-fMRI and EEG signal changes in response to visual stimulus frequency in humans. Magn Reson Med 49 1 (2003) 108-114
44. Kastrup A., et al. Changes of cerebral blood flow, oxygenation, and oxidative metabolism during graded motor activation. Neuroimage 15 1 (2002) 74-82
45. Anderson A.W., et al. Neonatal auditory activation detected by functional magnetic resonance imaging. Magn Reson Imaging 19 1 (2001) 1-5
46. Thomas C.G., and Menon R.S. Amplitude response and stimulus presentation frequency response of human primary visual cortex using BOLD EPI at 4 T. Magn Reson Med 40 2 (1998) 203-209
47. Shmuel A., et al. Sustained negative BOLD, blood flow and oxygen consumption response and its coupling to the positive response in the human brain. Neuron 36 6 (2002) 1195-1210
48. Birn R.M., Saad Z.S., and Bandettini P.A. Spatial heterogeneity of the nonlinear dynamics in the FMRI BOLD response. Neuroimage 14 4 (2001) 817-826
49. Miller K.L., et al. Nonlinear temporal dynamics of the cerebral blood flow response. Hum Brain Mapp 13 1 (2001) 1-12
50. Glover G.H. Deconvolution of impulse response in event-related BOLD fMRI. Neuroimage 9 4 (1999) 416-429
51. Inan S., et al. Hemodynamic correlates of stimulus repetition in the visual and auditory cortices: an fMRI study. Neuroimage 21 3 (2004) 886-893
52. Chen L.M., Friedman R.M., and Roe A.W. Optical imaging of SI topography in anesthetized and awake squirrel monkeys. J Neurosci 25 33 (2005) 7648-7659
53. Friston K.J. Imaging neuroscience: principles or maps?. Proc Natl Acad Sci U S A 95 3 (1998) 796-802
54. Garraghty P.E., Florence S.L., and Kaas J.H. Ablations of areas 3a and 3b of monkey somatosensory cortex abolish cutaneous responsivity in area 1. Brain Res 528 1 (1990) 165-169
55. Sripati A.P., et al. Spatiotemporal receptive fields of peripheral afferents and cortical area 3b and 1 neurons in the primate somatosensory system. J Neurosci 26 7 (2006) 2101-2114
56. Shmuel A., et al. Negative functional MRI response correlates with decreases in neuronal activity in monkey visual area V1. Nat Neurosci 9 4 (2006) 569-577
57. Logothetis N.K., et al. Neurophysiological investigation of the basis of the fMRI signal. Nature 412 6843 (2001) 150-157
58. Pouratian N., et al. Spatial/temporal correlation of BOLD and optical intrinsic signals in humans. Magn Reson Med 47 4 (2002) 766-776
59. Disbrow E.A., et al. Functional MRI at 1.5 Tesla: a comparison of the blood oxygenation level-dependent signal and electrophysiology. Proc Natl Acad Sci U S A 97 17 (2000) 9718-9723
60. Sawamura H., Orban G.A., and Vogels R. Selectivity of neuronal adaptation does not match response selectivity: a single-cell study of the FMRI adaptation paradigm. Neuron 49 2 (2006) 307-318
61. Arthurs O.J., and Boniface S.J. What aspect of the fMRI BOLD signal best reflects the underlying electrophysiology in human somatosensory cortex?. Clin Neurophysiol 114 7 (2003) 1203-1209
62. Hyder F., Rothman D.L., and Shulman R.G. Total neuroenergetics support localized brain activity: implications for the interpretation of fMRI. Proc Natl Acad Sci U S A 99 16 (2002) 10771-10776