Proceedings of the National Academy of Sciences · 2004 · 289 citations · 36 references
Life SciencesNeurobiologyNeuroscienceAgingMemoryMolecular NeuroscienceAge-related Physiologic ChangesBrain ImagingCerebral PhysiologyCognitive AgingHippocampal CircuitsHippocampal SystemsAge-related Brain ChangesBrain Function MappingDentate Gyrus FunctionHippocampal AgingHippocampal FunctionHippocampal PhysiologyImmediate Early GenesMemory Dysfunction
The hippocampal formation contains a distinct population of neurons organized into separate anatomical subregions. Each hippocampal subregion expresses a unique molecular profile accounting for their differential vulnerability to mechanisms of memory dysfunction. Nevertheless, it remains unclear which hippocampal subregion is most sensitive to the effects of advancing age. Here we investigate this question by using separate imaging techniques, each assessing different correlates of neuronal function. First, we used MRI to map cerebral blood volume, an established correlate of basal metabolism, in the hippocampal subregions of young and old rhesus monkeys. Second, we used in situ hybridization to map Arc expression in the hippocampal subregions of young and old rats. Arc is an immediate early gene that is activated in a behavior-dependent manner and is correlated with spike activity. Results show that the dentate gyrus is the hippocampal subregion most sensitive to the effects of advancing age, which together with prior studies establishes a cross-species consensus. This pattern isolates the locus of age-related hippocampal dysfunction and differentiates normal aging from Alzheimer's disease.
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Differences in the pattern of hippocampal neuronal loss in normal ageing and Alzheimer's disease
Mark J. West, Paul D. Coleman, Dorothy G. Flood et al. · The Lancet · 1994 · 1.3K citations · Full text
John F. Guzowski, Gregory L. Lyford, Gail D. Stevenson et al. · Journal of Neuroscience · 2000 · 1K citations · Full text