Memory
Memory functioning – broadly defined as the storage
and recall of past experience – is of major interest and importance in
cognitive neuroscience. The intensity of research in the area of memory has
been especially great in the past decade, when the fields of cogni-tive
psychology and neuropsychology converged to offer unified models of memory
functioning on the basis of experimentation in normal and brain-damaged humans,
as well as lesion studies in animals. Functional neuroimaging has also begun to
yield valu-able insights into the patterns of neuroanatomical connectivity
involved in aspects of memory. Because this field is relativelmassive, the
reader is referred to comprehensive sources for fur-ther details (Christianson,
1992; Squire and Butters, 1992).
Historically, the debate between the
localizationist and ho-listic views of neural processing has been nowhere
sharper than in the search for regionally specific entities involved in memory.
The search for the “engram” or memory trace led Lashley (1950) to conclude that
memories are distributed throughout the brain, not localized within a discrete
or unitary structure. The debate has been given a more sophisticated focus with
the realization that although there is regional specificity in aspects of
memory, the complexity of the processes requires multiple brain regions,
probably operating in a parallel fashion.
The initial contributions to the present knowledge
of mem-ory were from two methodologies. These are the lesion analytical method
and cognitive studies of normal individuals. The lesion analytical method has
contributed the most to an understandingof both the cognitive and
neuroanatomical aspects of memory functioning.
In the last 10 years, functional neuroimaging
techniques (particularly positron emission tomography [PET] and functional
magnetic resonance imaging [fMRI]) have become increasingly popular and provide
an alternative method of studying human cognition. These techniques have the
dual potential to validate existing models of memory and to suggest newer
theories based on patterns of anatomical connectivity observed during the
performance of memory tasks. Furthermore, unlike the lesion analytical method,
they afford the ability to observe cognitive processes in healthy human brains.
Neither PET nor fMRI di-rectly measures neural activity; rather, they rely on
changes in regional cerebral blood flow (rCBF) that result from the meta-bolic
demands of neural activity. As neural activity occurs, the demand for oxygen
causes an increase in the relative concentra-tion of deoxyhemoglobin in the
surrounding region.
There are several things to keep in mind when
consider-ing findings from neuroimaging studies. First, it is important to
remember that PET and fMRI are based on relative blood flow. Therefore, the
baseline task subtracted from the events of interest must be tightly controlled
to ensure that the finding is as specific as possible. Furthermore, although
functional neuroimaging can suggest brain regions functionally involved in
performing a cog-nitive operation, blood flow studies cannot suggest what is
unique about that brain region. Also, when distributed brain regions are
simultaneously activated, the technique itself does not immedi-ately reveal the
functional connectivity between those regions. Unlike the electrophysiological
studies of working memory, im-aging cannot suggest whether a brain region is in
a sense storing information or transmitting information or is in some other way
involved in the performance of an operation.
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