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The Journal of Neurophysiology Vol. 88 No. 1 July 2002, pp. 422-437
Copyright ©2002 by the American Physiological Society
Laboratory of Neuro Imaging, Department of Neurology, Division of Brain Mapping, University of California, Los Angeles, California 90095
Blood, Anne J.,
Nader Pouratian, and
Arthur W. Toga.
Temporally Staggered Forelimb Stimulation Modulates Barrel Cortex
Optical Intrinsic Signal Responses to Whisker Stimulation. J. Neurophysiol. 88: 422-437, 2002. Characterization of neurovascular relationships is
critical to accurate interpretation of functional neuroimaging data. We have previously observed spatial uncoupling of optical intrinsic signal
imaging (OIS) and evoked potential (EP) responses in rodent barrel
cortex following simultaneous whisker and forelimb stimulation, leading
to changes in OIS response magnitude. To further test the hypothesis
that this uncoupling may have resulted from "passive" overspill of
perfusion-related responses between functional regions, we conducted
the present study using temporally staggered rather than simultaneous
whisker and forelimb stimulation. This paradigm minimized overlap of
neural responses in barrel cortex and forelimb primary somatosensory
cortex (SI), while maintaining overlap of vascular response time
courses between regions. When contrasted with responses to 1.5-s
lone-whisker stimulation, staggered whisker and forelimb stimulation
resulted in broadening of barrel cortex OIS response time course in the
temporal direction of forelimb stimulation. OIS response peaks were
also temporally shifted toward the forelimb stimulation period;
time-to-peak was shorter (relative to whisker stimulus onset) when
forelimb stimulation preceded whisker stimulation and longer when
forelimb stimulation followed whisker stimulation. In contrast with OIS
and EP magnitude decreases previously observed during simultaneous
whisker/forelimb stimulation, barrel cortex OIS response magnitude
increased during staggered stimulation and no detectable changes in
underlying EP activity were observed. Spatial extent of barrel cortex
OIS responses also increased during staggered stimulation. These
findings provide further evidence for spatial uncoupling of OIS and EP
responses, and emphasize the importance of temporal stimulus properties
on the effects of this uncoupling. It is hypothesized that spatial uncoupling is a result of passive overspill of perfusion-related responses into regions distinct from those which are functionally active. It will be important to consider potential influences of this
uncoupling when designing and interpreting functional imaging studies
that use hemodynamic responses to infer underlying neural activity.
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