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Poster Sessions<br />

weeks) after experimental kindling induced epilepsy. The data indicate that there is considerable neuroplasticity and development of new pathways during<br />

the progression of epilepsy. Whether comparable plasticity of cortical maps is present in humans should be tested using fMRI in future studies, considering<br />

that such seizure-induced changes may be involved in producing interictal behavioural disturbances.<br />

1207. Layer-Specific FMRI of Photic Stimulation in the Rat Retina at 11.7 T<br />

Yen-Yu Ian Shih 1 , Bryan H. De La Garza 1 , William J. Lavery 1 , Eric R. Muir 1,2 , Timothy Q. Duong 1<br />

1 Research Imaging Institute, Ophthalmology/Radiology, University of Texas Health Science Center at San Antonio, San Antonio, TX,<br />

United States; 2 Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States<br />

The retina is about 276 micron thick including the choroid and has highly organized laminar structures. This study reports, for the first time, the feasibility of<br />

high-resolution blood-volume fMRI to image layer specific (retinal and choroidal) visual responses in the rat retina at 11.7T up to 40x40x600 micron<br />

nominal resolution. Given that the choroid is behind the retina and the retinal pigment epithelium, it is generally inaccessible by optical techniques. Bloodvolume<br />

fMRI thus could provide a unique means to evaluate lamina-specific functional changes in the rat retina where many retinal disease models are<br />

readily available.<br />

1208. Pass-Band Balanced Steady State Free Precession Functional MRI of the Mouse Retina<br />

Eric Raymond Muir 1,2 , Sung-Hong Park 3 , Timothy Q. Duong 2<br />

1 Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States; 2 Research Imaging Institute,<br />

Ophthalmology/Radiology, UT Health Science Center San Antonio, San Antonio, TX, United States; 3 Research Imaging Institute,<br />

Radiology, UT Health Science Center San Antonio, San Antonio, TX, United States<br />

BOLD fMRI of the thin retina with the widely used EPI acquisition is challenging because the eye is a region of large magnetic inhomogeneity and highresolution<br />

EPI is pushing the limits of gradient performance, resulting in susceptibility-induced signal drop out and image distortion. To overcome these<br />

limitations, we implemented a pass-band balanced steady state free precession (bSSFP) sequence for fMRI of the mouse retina at 45x45x500 µm. bSSFP has<br />

comparable temporal resolution and SNR per unit time as EPI, without the artifacts common in EPI. bSSFP fMRI could reliably detect layer-specific<br />

responses to hypoxic challenge in the mouse retina.<br />

1209. Simultaneous FMRI and Long-Term in Vivo Electrochemistry (LIVE): Identifying the Neurochemical<br />

Correlates of Functional Imaging Signals<br />

John Lowry 1 , Karen Griffin 2 , Stephen McHugh 3 , Nicola Sibson 4<br />

1 Department of Chemistry, National University of Ireland, Maynooth, Ireland; 2 University College Dublin, Ireland; 3 Department of<br />

Experimental Psychology, University of Oxford, Oxford, United Kingdom; 4 Gray Institute for Radiation Oncology and Biology,<br />

University of Oxford, Oxford, Oxfordshire, United Kingdom<br />

Long-term in-vivo electrochemistry (LIVE) enables real-time measurement of brain metabolites. Here we have simultaneously obtained BOLD fMRI and<br />

amperometric LIVE tissue oxygen data from rat cerebral cortex, during both increases and decreases in inspired oxygen. BOLD and tissue oxygen<br />

measurements demonstrated close correlation during both complete oxygen removal (negative responses) and increases in inspired oxygen (positive<br />

responses). Our findings demonstrate the feasibility of obtaining real-time metabolite information during fMRI acquisition. The results show that the BOLD<br />

signal provides a close correlate of the tissue oxygen dynamics or, alternatively, that tissue oxygen concentration can predict the magnitude of the BOLD<br />

response.<br />

1210. Evaluation of Cerebral Energy Demand During Graded Hypercapnia<br />

Stefan Alexandru Carp 1 , Maria Angela Franceschini 1 , David Alan Boas 1 , Young Ro Kim 1<br />

1 Martinos Center/Radiology, Massachusetts General Hospital, Charlestown, MA, United States<br />

The cerebral metabolic rate of oxygen (CMRO 2 ) is a physiological parameter closely linked to neural activation as well as to various disease states.<br />

Hypercapnic calibration is used to calibrate the BOLD-CBF-CBV relationship under the assumption of iso-metabolic blood flow increase during CO 2<br />

inhalation. Simultaneous near infrared optical measurements of cerebral blood volume, blood flow and oxygen extraction can also be used to monitor<br />

CMRO 2 changes, albeit at low spatial resolution. We use these optical measurements during graded hypercapnia to test the iso-metabolic assumption, and<br />

demonstrate an apparent increase in brain metabolism at higher inhaled CO 2 levels.<br />

1211. Dissociation of BOLD and Local Field Potentials<br />

Wen-Ju Pan 1 , Matthew Magnuson 1 , Garth Thompson 1 , Waqas Majeed 1 , Dieter Jaeger 2 , Shella Keilholz 1<br />

1 BME, Georgia Institute of Technology / Emory University, Atlanta, GA, United States; 2 Biology, Emory University, Atlanta, GA,<br />

United States<br />

To examine what extent consistence of the measurements between BOLD fMRI and local field potential (LFP), we evaluated BOLD and LFP<br />

simultaneously in rat somatosensory cortex with a combined measurement technique. The preliminary results indicated a dissociation between BOLD and<br />

LFP during low-level neural activity, which might mirror the limitation of neurovascular coupling, the bridge between BOLD and neural activity.<br />

1212. TR and TE Dependence on Low Frequency BOLD Fluctuations<br />

Matthew Evan Magnuson 1 , Wenju Pan 1 , Waqas Majeed 1 , Garth Thompson 1 , Shella Keilholz 1<br />

1 Biomedical Engineering, Georgia Institute of Technology / Emory University, Atlanta, GA, United States<br />

Low freqnecy fluctuations in resting state BOLD data have often been used to map functional connectivity in the rat brain. These low frequency BOLD<br />

fluctuations contain contributions from CBF, CBV, and CMRO2. Each of these components have unique physiological time signatures and effective echo<br />

times; therefore, modification of the TR and TE used in resting state scans should result in altered contributions from each BOLD component. In this study<br />

we examine the dependence of the selection of the TR and TE variables on low frequency resting state data.

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