Every sensory modality in the macaque is served by a series of cortical stations, each of which processes the sensory signal in turn. Signals in the later stations, located in the anterior temporo-insular cortex, can activate a circuit that runs through the limbic system to the modulatory meurochemical systems (e.g. cholinergic, noradrenergic, etc.) and back to the sensory cortical stations. We have proposed that as a result of the action of this circuit on neurochemical release in sensory cortex, some of the neurons whose signals have just represented the sensory stimulus become linked together in a cell assembly that serves as the stored representation of that stimulus. Recognition, say of an object, occurs when an assembly formed on a first presentation of the object is reactivated by its re- presentation on a second occasion. also, once formed, that assembly can be linked to assemblies representing other stimuli and other events, such as a food reward or a location, thereby investing the recognized object with meaning. The linkage involved in object-reward association appears to be mediated mainly by a limbo-neurochemical circuit running through the amygdala, the medial dorsal thalamic nucleus, orbital frontal cortex, and the basal nucleus of Meynert. Similarly, the linkage involved in object- place association seems to be mediated mainly by a second, parallel limbo- neurochemical circuit running through the hippocampus, the anterior thalamic nuclei, cingulate cortex, and the medial septal and diagonal band nuclei. Each of these subcortical circuits has reciprocal connections with one pair or the other of the cortical cell assemblies described above. Thus, if these circuits have been activated, the sight of the object on a second occasion can lead not only to its recognition but also to recall of both the food reward and the spatial location with which the object had been associated. Recognition and recall are two forms of stimulus memory, both of which can be distinguished from habit formation. The latter form of learning involves stimulus-response association and depends largely on interactions between the cerebral cortex and the basal ganglia.
| de Haan, Michelle; Mishkin, Mortimer; Baldeweg, Torsten et al. (2006) Human memory development and its dysfunction after early hippocampal injury. Trends Neurosci 29:374-81 |
| Brandt, Karen R; Gardiner, John M; Vargha-Khadem, Faraneh et al. (2006) Using semantic memory to boost 'episodic' recall in a case of developmental amnesia. Neuroreport 17:1057-60 |
| Belcher, Annabelle M; Harrington, Rebecca A; Malkova, Ludise et al. (2006) Effects of hippocampal lesions on the monkey's ability to learn large sets of object-place associations. Hippocampus 16:361-7 |
| de Haan, Michelle; Wyatt, John S; Roth, Simon et al. (2006) Brain and cognitive-behavioural development after asphyxia at term birth. Dev Sci 9:350-8 |
| Saunders, Richard C; Mishkin, Mortimer; Aggleton, John P (2005) Projections from the entorhinal cortex, perirhinal cortex, presubiculum, and parasubiculum to the medial thalamus in macaque monkeys: identifying different pathways using disconnection techniques. Exp Brain Res 167:1-16 |
