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J Neurophysiol 95: 3164-3170, 2006. First published January 4, 2006; doi:10.1152/jn.00400.2005
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Light Stimulus Frequency Dependence of Activity in the Rat Visual System as Studied With High-Resolution BOLD fMRI

Nadja Van Camp1, Marleen Verhoye1,2, Chris I. De Zeeuw3 and Annemie Van der Linden1

1Bio-Imaging Lab, University of Antwerp, Antwerp, Belgium; 2Visielab, University of Antwerp; 3Department of Neuroscience, Erasmus Medical College, Rotterdam, The Netherlands

Submitted 19 April 2005; accepted in final form 22 December 2005

The neurophysiology of the rodent visual system has mainly been investigated by invasive and ex-vivo techniques providing fragmented data. This area of research has been deprived of functional MRI studies based on blood oxygenation level dependent (BOLD) contrast, which allows a whole brain approach with a high spatial and temporal resolution. In the present study, we looked at the neurovascular response properties of the visual system of the pigmented rat, focusing on the visual cortex (VC), the superior colliculus (SC) and the flocculus-paraflocculus of the cerebellum (FL-PFL), using BOLD fMRI under domitor anesthesia. Visual stimulation was performed monocularly or binocularly while flashing light from a strobe unit was presented. For each structure, we assessed the flashing frequency that evoked the optimal BOLD response: Neither the VC nor the FL-PFL displayed frequency dependence during monocular visual stimulation, but were most sensitive to low frequencies (1–5 Hz) when flashing light was provided binocularly. The SC responded optimally to high flashing rates (8–12 Hz) during both monocular and binocular stimulation. The signal intensity changes in the VC and FL-PFL were locked to the stimulation period, whereas the BOLD response in the SC showed a similar onset but a very slow recovery at offset. The VC and FL-PFL, but not the SC, showed signs of binocular competition. The observed correlation between frequency-dependent responses of different visual areas during binocular visual presentation suggests a functional relationship between the VC and FL-PFL rather than between the SC and FL-PFL.


Address for reprint requests and other correspondence: Nadja Van Camp, Bio-Imaging Lab, University of Antwerp, Campus Middelheim, Groenenborgerlaan 171, 2020 Antwerp, Belgium. (E-mail nadja.vancamp{at}ua.ac.be)




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