The majority of neurophysiological studies
in conscious primates use craniotomies and recording
chambers to access the same cortical territory for
up to several years. In this technique, stereotaxic
references are adequate for coarse positioning of
the recording chamber relative to the brain area under
study. However, individual anatomical variations,
chamber placement errors, and changes over time degrade
our ability to localize recording sites using conventional
methods, particularly in regions of brain with complex
anatomy such as the cerebral cortex. As a result,
labs increasingly rely on functional criteria to characterize
recording sites. Since functional criteria are rarely
standardized, this strategy can make it difficult
for the neuroscience community at large to reconcile
results obtained from different labs.
We have developed a robust, practical method to localize
single unit recordings to within 1mm using magnetic
resonance imaging (MRI). After chamber placement,
a high-resolution (0.5-0.8 mm^3) T1-weighted MRI is
acquired. The image includes the brain and a specially
designed, MR-lucent cylinder marking the position,
orientation and dimensions of the recording chamber.
The affine transformations required to project data
from the native MRI into either chamber-aligned or
stereotactic views are computed using automated, iterative
procedures. Our lab has used this method to generate
individualized chamber-aligned atlases (n=15) to guide
single unit recording sessions (n=~75) and MnCl injections
(n=6). These experiments have provided physiological
and MRI evidence that our localization precision,
which should scale with our MRI resolution, is <1mm.
The new method is particularly suited to single unit/fMRI
correlative studies and to the study of functional
organization across the cortical surface in relation
to gross anatomical features.
Support Contributed By: McDonnell Ctr for Higher
Brain Function
|