Implementation of spin-echo blood oxygen level-dependent (BOLD) functional MRI in birds

NMR in Biomedicine

Volumn 23, Issue 9, 2010, Pages 1027-1032

  Poirier, Colline ^a   Verhoye, Marleen ^a   Boumans, Tiny ^a   Van Der Linden, Annemie ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Auditory; Birdsong; BOLD; FMRI; Songbird; Spin echo

Indexed keywords

AUDITORY; BIRDSONG; BOLD; FMRI; SONGBIRD; SPIN ECHO;

BLOOD; MAGNETIC FIELDS; OXYGEN; SIGNAL TO NOISE RATIO;

BIRDS;

ARTICLE; AUDITORY CORTEX; AUDITORY STIMULATION; CONTROLLED STUDY; FINCH; FUNCTIONAL MAGNETIC RESONANCE IMAGING; GRADIENT ECHO BLOOD OXYGEN LEVEL DEPENDENT FUNCTIONAL MAGNETIC RESONANCE IMAGING; HEARING; LEARNING; MALE; MESENCEPHALON; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION; PRIORITY JOURNAL; SIGNAL NOISE RATIO; SPIN ECHO BLOOD OXYGEN LEVEL DEPENDENT FUNCTIONAL MAGNETIC RESONANCE IMAGING;

ANIMALS; BIRDS; BRAIN MAPPING; CEREBROVASCULAR CIRCULATION; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; OXYGEN; VOCALIZATION, ANIMAL;

ANIMALIA; AVES; PASSERI; TAENIOPYGIA GUTTATA;

EID: 79251510248     PISSN: 09523480     EISSN: 10991492     Source Type: Journal    
DOI: 10.1002/nbm.1525     Document Type: Article

References (23)

1. Van der Linden A, Van Camp N, Ramos-Cabrer P, Hoehn M. Current status of functional MRI on small animals: application to physiology, pathophysiology, and cognition. NMR Biomed. 2007; 20: 522-545.
2. Yacoub E, Duong TQ, Van De Moortele PF, Lindquist M, Adriany G, Kim SG, Uǧurbil K, Hu X. Spin-echo fMRI in humans using high spatial resolutions and high magnetic fields. Magn Reson Med. 2003; 49: 655-664.
3. Yacoub E, Van De Moortele PF, Shmuel A, Uǧurbil K. Signal and noise characteristics of Hahn SE and GE BOLD fMRI at 7 T in humans. Neuroimage. 2005; 24: 738-750.
4. Van Meir V, Boumans T, De Groof G, Van Audekerke J, Smolders A, Scheunders P, Sijbers J, Verhoye M, Balthazart J, Van der Linden A. Spatiotemporal properties of the BOLD response in the songbirds' auditory circuit during a variety of listening tasks. Neuroimage. 2005; 25: 1242-1255.
5. Boumans T, Theunissen FE, Poirier C, Van Der Linden A. Neural representation of spectral and temporal features of song in the auditory forebrain of zebra finches as revealed by functional MRI. Eur J Neurosci. 2007; 26: 2613-2626.
6. Boumans T, Gobes SMH, Poirier C, Theunissen FE, Vandersmissen L, Pintjens W, Verhoye M, Bolhuis JJ, Van der Linden A, Functional MRI of auditory responses in the zebra finch forebrain reveals a hierarchical organisation based on signal strength but not selectivity. PLoS ONE. 2008; 3: e 3184.
7. Boumans T, Vignal C, Smolders A, Sijbers J, Verhoye M, Van Audekerke J, Mathevon N, Van der Linden A. Functional magnetic resonance imaging in zebra finch discerns the neural substrate involved in segregation of conspecific song from background noise. J Neurophysiol. 2008; 99: 931-938.
8. Voss HU, Tabelow K, Polzehl J, Tchernichovski O, Maul K, Salgado-Commissariat D, Ballon D, Helekar SA. Functional MRI of the zebra finch brain during song stimulation suggests a lateralized response topography. Proc Natl Acad Sci USA. 2007; 104: 10667-10672.
9. Maul KK, Voss HU, Parra LC, Salgado-Commissariat D, Ballon D, Tchernichovski O, Helekar SA. The development of stimulus specific auditory responses requires song exposure in male but not female zebra finches. Dev Neurobiol. 2010; 70: 28-40.
10. Poirier C, Boumans T, Verhoye M, Balthazart J, Van der Linden A. Own-song recognition in the songbird auditory pathway: selectivity and lateralization. J Neurosci. 2009; 29: 2252-2258.
11. Van der Linden A, Van Meir V, Boumans T, Poirier C, Balthazart J. MRI in small brains displaying extensive plasticity. Trends Neurosci. 2009; 32: 257-266.
12. Poirier C, Vellema M, Verhoye M, Van Meir V, Wild JM, Balthazart J, Van Der Linden A. A three-dimensional MRI atlas of the zebra finch brain in stereotaxic coordinates. Neuroimage. 2008; 41: 1-6.
13. Maes F, Collignon A, Vandermeulen D, Marchal G, Suetens P. Multimodality image registration by maximization of mutual information. IEEE Trans Med Imaging. 1997; 16: 187-198.
14. Vanhoutte G, Verhoye M, Van der Linden A. Changing body temperature affects the T2* signal in the rat brain and reveals hypothalamic activity. Magn Reson Med. 2006; 55: 1006-1012.
15. Keilholz SD, Silva AC, Raman M, Merkle H, Koretsky AP. Functional MRI of the rodent somatosensory pathway using multislice echo planar imaging. Magn Reson Med. 2004; 52: 89-99.
16. Keilholz SD, Silva AC, Raman M, Merkle H, Koretsky AP, and BOLD. CBV-weighted functional magnetic resonance imaging of the rat somatosensory system. Magn Reson Med. 2006; 55: 316-324.
17. Zhao F, Wang P, Kim SG. Cortical depth-dependent gradient-echo and spin-echo BOLD fMRI at 9.4 T. Magn Reson Med. 2004; 51: 518-524.
18. Harel N, Lin J, Moeller S, Uǧurbil K, Yacoub E. Combined imaging-histological study of cortical laminar specificity of fMRI signals. Neuroimage. 2006; 29: 879-887.
19. Lee SP, Silva AC, Uǧurbil K, Kim SG. Diffusion-weighted spin-echo fMRI at 9.4 T: microvascular/tissue contribution to BOLD signal changes. Magn Reson Med. 1999; 42: 919-928.7.
20. Duong TQ, Yacoub E, Adriany G, Hu X, Uǧurbil K, Kim SG. Microvascular BOLD contribution at 4 and 7 T in the human brain: gradient-echo and spin-echo fMRI with suppression of blood effects. Magn Reson Med. 2003; 49: 1019-1027.
21. Uludaǧ K, Müller-Bierl B, Uǧurbil K. An integrative model for neuronal activity-induced signal changes for gradient and spin echo functional imaging. Neuroimage. 2009; 48: 150-165.
22. Goloshevsky AG, Silva AC, Dodd SJ, Koretsky AP. BOLD fMRI and somatosensory evoked potentials are well correlated over a broad range of frequency content of somatosensory stimulation of the rat forepaw. Brain Res. 2008; 1195: 67-76.
23. Kida I, Yamamoto T. Stimulus frequency dependence of blood oxygenation level-dependent functional magnetic resonance imaging signals in the somatosensory cortex of rats. Neurosci Res. 2008; 62: 25-31.