Extensive neural connections between the anterior thalamic nuclei (ATN) and the hippocampal system may explain the overlapping amnesic syndromes associated with diencephalic and medial temporal lobe brain injury. Despite the debilitating nature of the diencephalic amnesia, treatments for this condition are lacking. In rats, lesions to the ATN or hippocampus generally produce similar memory deficits, which further implicate these structures in a single functional memory system. First evidence is presented here that seemingly permanent and robust spatial working memory deficits seen after lesions to the ATN in rats are ameliorated by environmental intervention and pharmacological treatment. Post-operative housing of ATN-lesioned rats for 30 days in enriched environment resulted in marked improvements in performance on the spatial working memory task in the cross-maze irrespective of whether rats were exposed to enrichment immediately after surgery or enrichment was delayed by 40 days post-surgery. Long-term beneficial effects of enrichment were also demonstrated. Behavioural improvements were observed when Cerebrolysin - a neurotrophic compound - was injected intraperitoneally for 30 days post-surgery. The combination of enrichment and Cerebrolysin treatment was more effective in inducing recovery on a delayed memory test in the cross-maze task. The influence of enrichment and Cerebrolysin on the neural changes produced by ATN lesions was examined utilising an immediate early gene marker c-fos. Replicating previous studies, ATN lesions produced marked hypoactivity in the retrosplenial cortex, but this effect was not reversed by either enrichment or Cerebrolysin. Unexpectedly, enrichment produced further hypoactivation in this region. Although lesion-induced deficits in a radial-arm maze spatial discrimination task were not improved by enrichment, a related study in our laboratory showed that spatial reference memory can also be improved by enrichment in ATN rats. The current research provides strong support for potential opportunities for therapeutic intervention in the human domain.

Conventional theories of diencephalic amnesia have focused on a single thalamic region as a critical factor in the origins of anterograde amnesia. A more contemporary view is that different thalamic regions might contribute in unique ways to normal diencephalic functioning and therefore provide distinct contributions to the learning and memory. This study directly compared the effects of AT and MT lesions on a spatial pattern separation task, a spatial working memory task and a conditioned place preference task. AT lesions but not MT lesions produces deficits on the spatial working memory task on a cheeseboard. No group AT, MT or control rats acquired a conditioned place preference on the AT/MT lesion conditioned place preference task. Furthermore, this study determined the effect of systematic procedural variations on control rats in a conditioned place preference control task. The only variation that acquired a condition place preference was a separate arms conditioned place preference with one pre-exposure and three training trials. The results of this study provide new information regarding the role of thalamic lesions in spatial memory and suggests a revision of the current theories regarding learning and memory to incorporate the thalamic involvement that has been highlighted

Conventional theories of diencephalic amnesia have focused on a single thalamic region as a critical factor in the origins of anterograde amnesia. A more contemporary view is that different thalamic regions might contribute in unique ways to normal diencephalic functioning and therefore provide distinct contributions to the learning and memory. This study directly compared the effects of AT and MT lesions on a spatial pattern separation task, a spatial working memory task and a conditioned place preference task. AT lesions but not MT lesions produces deficits on the spatial working memory task on a cheeseboard. No group AT, MT or control rats acquired a conditioned place preference on the AT/MT lesion conditioned place preference task. Furthermore, this study determined the effect of systematic procedural variations on control rats in a conditioned place preference control task. The only variation that acquired a condition place preference was a separate arms conditioned place preference with one pre-exposure and three training trials. The results of this study provide new information regarding the role of thalamic lesions in spatial memory and suggests a revision of the current theories regarding learning and memory to incorporate the thalamic involvement that has been highlighted

Diencephalic amnesia is thought to be the result of damage to a single thalamic structure that is responsible for the memory impairment. However, an alternative view is that different thalamic structures contribute to the memory impairment in subtly different ways. Paired-associate learning is one important measure of learning and memory that is highly sensitive to disruption in people with amnesia or dementia. The current study will investigate the influence of lesions to two thalamic subregions, the anterior thalamic nuclei (AT) and the lateral thalamic nuclei (LT) in an object-odour paired associate learning task. Each of these subregions has been suggested by the literature as critical for amnesia after thalamus injury. The current study does not involve a place/ space component. Both AT and LT lesions caused impairments in the object-odour paired associate task, but not in the simple discrimination tasks. The results of this study provide new evidence to suggest that the anterior thalamic region may be responsible for more than spatial memory processing. This result is inconsistent with those of Aggleton & Brown (1999) that consider the AT to be part of an 'extended hippocampal system'. The deficits observed from LT lesions in this study provide new insight into the lateral thalamic region's role in pattern processing.

Diencephalic amnesia is thought to be the result of damage to a single thalamic structure that is responsible for the memory impairment. However, an alternative view is that different thalamic structures contribute to the memory impairment in subtly different ways. Paired-associate learning is one important measure of learning and memory that is highly sensitive to disruption in people with amnesia or dementia. The current study will investigate the influence of lesions to two thalamic subregions, the anterior thalamic nuclei (AT) and the lateral thalamic nuclei (LT) in an object-odour paired associate learning task. Each of these subregions has been suggested by the literature as critical for amnesia after thalamus injury. The current study does not involve a place/ space component. Both AT and LT lesions caused impairments in the object-odour paired associate task, but not in the simple discrimination tasks. The results of this study provide new evidence to suggest that the anterior thalamic region may be responsible for more than spatial memory processing. This result is inconsistent with those of Aggleton & Brown (1999) that consider the AT to be part of an 'extended hippocampal system'. The deficits observed from LT lesions in this study provide new insight into the lateral thalamic region's role in pattern processing.