Age-related changes in rostral basal forebrain cholinergic and GABAergic projection neurons: relationship with spatial impairment

• DOI: 10.1016/j.neurobiolaging.2012.06.013
• Publication Date: 2012-07-18T21:05:17Z
• Authors: Cristina Bañuelos; Candi L. LaSarge; Joseph A. McQuail; John J. Hartman; Ryan J. Gilbert; Brandi K. Ormerod; Jennifer L. Bizon
• Keywords: Male; 0301 basic medicine; Aging; Glutamate Decarboxylase; Antigens, Nuclear; Nerve Tissue Proteins; Hippocampus; Immunohistochemistry; Cholinergic Neurons; Rats, Inbred F344; Choline O-Acetyltransferase; Rats; 03 medical and health sciences; Prosencephalon; Memory; Animals; GABAergic Neurons; Maze Learning

Both cholinergic and GABAergic projections from the rostral basal forebrain contribute to hippocampal function and mnemonic abilities. While dysfunction of cholinergic neurons has been heavily implicated in age-related memory decline, significantly less is known regarding how age-related changes in codistributed GABAergic projection neurons contribute to a decline in hippocampal-dependent spatial learning. In the current study, confocal stereology was used to quantify cholinergic (choline acetyltransferase [ChAT] immunopositive) neurons, GABAergic projection (glutamic decarboxylase 67 [GAD67] immunopositive) neurons, and total (neuronal nuclei [NeuN] immunopositive) neurons in the rostral basal forebrain of young and aged rats that were first characterized on a spatial learning task. ChAT immunopositive neurons were significantly but modestly reduced in aged rats. Although ChAT immunopositive neuron number was strongly correlated with spatial learning abilities among young rats, the reduction of ChAT immunopositive neurons was not associated with impaired spatial learning in aged rats. In contrast, the number of GAD67 immunopositive neurons was robustly and selectively elevated in aged rats that exhibited impaired spatial learning. Interestingly, the total number of rostral basal forebrain neurons was comparable in young and aged rats, regardless of their cognitive status. These data demonstrate differential effects of age on phenotypically distinct rostral basal forebrain projection neurons, and implicate dysregulated cholinergic and GABAergic septohippocampal circuitry in age-related mnemonic decline.