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1.
Neuroscience ; 137(4): 1119-30, 2006.
Article in English | MEDLINE | ID: mdl-16343780

ABSTRACT

Latent inhibition is a form of negative priming in which repeated non-reinforced pre-exposures to a stimulus retard subsequent learning about the predictive significance of that stimulus. The nucleus accumbens shell and the anatomical projection it receives from the hippocampal formation have been attributed a pivotal role in the control or regulation of latent inhibition expression. A number of studies in rats have demonstrated the efficacy of selective shell lesions to disrupt latent inhibition in different associative learning paradigms, including conditioned active avoidance and conditioned emotional response. Here, we extended the test to the conditioned taste aversion paradigm, in which the effect of direct hippocampal damage on latent inhibition remains controversial. We demonstrated the expected effect of selective shell lesions on latent inhibition of conditioned emotional response and of conditioned active avoidance, before evaluating in a separate cohort of rats the effect of comparable selective lesions on latent inhibition of conditioned taste aversion: a null effect of the lesions was first obtained using parameters known to be sensitive to amphetamine treatment, then an enhancement of latent inhibition was revealed with a modified conditioned taste aversion procedure. Our results show that depending on the associative learning paradigm chosen, shell lesions can disrupt or enhance the expression of latent inhibition; and the pattern is reminiscent of that seen following hippocampal damage.


Subject(s)
Conditioning, Psychological , Nucleus Accumbens/physiology , Taste , Animals , Brain Mapping , Nucleus Accumbens/anatomy & histology , Nucleus Accumbens/pathology , Rats , Rats, Wistar
2.
Neuroscience ; 127(2): 289-300, 2004.
Article in English | MEDLINE | ID: mdl-15262320

ABSTRACT

The present study was designed to assess the possibility that sub-total ventral hippocampal lesions might leave intact a mechanism for only highly accurate navigation, whereas sub-total dorsal hippocampal lesions might leave intact a mechanism only for less precise navigation. Animals with selective dorsal, ventral or complete hippocampal lesions were tested in a water maze, in which the target platform was moved from trial to trial, but always within a defined area, instead of being at a fixed location. Hence, an animal that searched at exactly the point where the platform had been found on a previous trial would be disadvantaged, in comparison with an animal that searched in the right general area. This might favor animals capable of less precise navigation over those with very precise navigational abilities. In subsequent phases of the experiment, we additionally assessed, for comparison, performance with a fixed platform location, reversal learning in the water-maze, and performance on an elevated T-maze. Our results revealed no sign of any qualitative difference between the effects of the selective sub-total lesions when the water maze hidden platform location was varied within the defined area, and the effects in subsequent more conventionally used tests. Ventral hippocampal damage never led to a performance deficit. Dorsal hippocampal damage led to significantly poorer performance in only some test phases, and never led to any sign of improved performance.


Subject(s)
Hippocampus/physiopathology , Memory Disorders/physiopathology , Memory/physiology , Neural Pathways/physiopathology , Space Perception/physiology , Animals , Behavior, Animal/physiology , Denervation , Disease Models, Animal , Hippocampus/drug effects , Hippocampus/pathology , Male , Maze Learning/physiology , Memory Disorders/chemically induced , Memory Disorders/pathology , Motor Activity/physiology , Neural Pathways/drug effects , Neural Pathways/pathology , Neurotoxins , Rats
3.
Neurosci Biobehav Rev ; 28(3): 273-83, 2004 May.
Article in English | MEDLINE | ID: mdl-15225971

ABSTRACT

The amnestic effects of hippocampal lesions are well documented, leading to numerous memory-based theories of hippocampal function. It is debatable, however, whether any one of these theories can satisfactorily account for all the consequences of hippocampal damage: Hippocampal lesions also result in behavioural disinhibition and reduced anxiety. A growing number of studies now suggest that these diverse behavioural effects may be associated with different hippocampal subregions. There is evidence for at least two distinct functional domains, although recent neuroanatomical studies suggest this may be an underestimate. Selective lesion studies show that the hippocampus is functionally subdivided along the septotemporal axis into dorsal and ventral regions, each associated with a distinct set of behaviours. Dorsal hippocampus has a preferential role in certain forms of learning and memory, notably spatial learning, but ventral hippocampus may have a preferential role in brain processes associated with anxiety-related behaviours. The latter's role in emotional processing is also distinct from that of the amygdala, which is associated specifically with fear. Gray and McNaughton's theory can in principle incorporate these apparently distinct hippocampal functions, and provides a plausible unitary account for the multiple facets of hippocampal function.


Subject(s)
Anxiety/physiopathology , Brain Mapping , Fear/physiology , Hippocampus/physiology , Memory/physiology , Animals , Hippocampus/anatomy & histology , Hippocampus/physiopathology , Humans
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