K. Grill-spector et R. Malach, fMR-adaptation: a tool for studying the functional properties of human cortical neurons, ACT PSYCHOL, 107(1-3), 2001, pp. 293-321
The invariant properties of human cortical neurons cannot be studied direct
ly by fMRI due to its limited spatial resolution. One voxel obtained from a
fMRI scan contains several hundred thousands neurons. Therefore, the fMRI
signal may average out a heterogeneous group of highly selective neurons. H
ere, we present a novel experimental paradigm for fMRI, functional magnetic
resonance-adaptation (fMR-A), that enables to tag specific neuronal popula
tions within an area and investigate their functional properties. This appr
oach contrasts with conventional mapping methods that measure the averaged
activity of a region. The application of fMR-A to study the functional prop
erties of cortical neurons proceeds in two stages: First, the neuronal popu
lation is adapted by repeated presentation of a single stimulus. Second, so
me property of the stimulus is varied and the recovery from adaptation is a
ssessed. If the signal remains adapted, it will indicate that the neurons a
re invariant to that attribute. However, if the fMRI signal will recover fr
om the adapted state it would imply that the neurons are sensitive to the p
roperty that was varied. Here, an application of fMR-A for studying the inv
ariant properties of high-order object areas (lateral occipital complex - L
OG) to changes in object size, position, illumination and rotation is prese
nted. The results show that LOC is less sensitive to changes in object size
and position compared to changes of illumination and viewpoint. fMR-A can
be extended to other neuronal systems in which adaptation is manifested and
can be used with event-related paradigms as well. By manipulating experime
ntal parameters and testing recovery from adaptation it should be possible
to gain insight into the functional properties of cortical neurons which ar
e beyond the spatial resolution limits imposed by conventional fMRI. (C) 20
01 Published by Elsevier Science B.V.