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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: Neuroimage. 2013 Apr 22;78:385–395. doi: 10.1016/j.neuroimage.2013.04.045

Fig. 2. Intravascular and extravascular contributions to functional R1ρ change in the cat visual cortex.

Fig. 2

A slightly bright band (indicated by black arrows) within the gray matter (outlined in green) in high-resolution T1-weighted EPI image (A) indicates cortical layer IV (Kim and Kim, 2011). Pixels along the white band (yellow) were chosen for quantitative analyses of cat's functional studies (B). All active pixels were overlaid in color on their respective baseline images (C-F), and the vertical grayscale bar indicates the baseline R1ρ values (for E and F). Functional percentage signal change maps were obtained by T2-weighted (TSL = 0, C) and T1ρ-weighted fMRI (TSL = 50 ms and ω1 = ~500 Hz, D) without MION during visual stimulation. Higher changes were observed in T1ρ-weighted fMRI, indicating an increase in T1ρ (decrease in R1ρ). To determine the blood contribution, R1ρ change maps obtained without (E) and with (F) 5 mg/kg MION were compared. An increase in R1ρ at the surface of the cortex is due to a volume fraction change between tissue and CSF, while a decrease in R1ρ is located at the middle of the cortex. (G) At the middle cortical ROI (yellow pixels in B), the functional R2 change (ΔR2) is nearly suppressed with MION injection, whereas ΔR1ρ only decreases slightly.