Beta-amyloid peptide-induced modifications in α7 nicotinic acetylcholine receptor immunoreactivity in the hippocampus of the rat: Relationship with GABAergic and calcium-binding proteins perikarya

• Published in: Brain research bulletin 2008-03, Vol.75 (5), p.533-544
• Main Authors: Arévalo-Serrano, J, Sanz-Anquela, J.M, Gonzalo-Ruiz, A
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Beta-amyloid peptide; Hippocampus; Neurology; Neurotoxicity; Nicotinic acetylcholine receptors; Posterior cingulate cortex
• ISSN: 0361-9230; 1873-2747
• DOI: 10.1016/j.brainresbull.2007.09.003

Abstract The effects of the injected beta-amyloid (Aβ) protein on the α7 subtype of nicotinic acetylcholine receptor protein (α7nAChR) in the hippocampus were studied in rats. Injections of Aβ into the retrosplenial cortex resulted in a decrease in α7nAChR-immunoreactivity in the hippocampus. Quantitative analysis revealed a significant reduction in α7nAChR-immunoreactivity in the dorsal part of the CA1 ipsilateral to the Aβ-injected side as compared to the corresponding hemisphere of non-treated control animals and with that seen in the contralateral hemisphere, which corresponds to the control (PBS)-injected side. A significant decrease in α7nAChR-immunoreactivity was also found in the dorsal part of the ipsilateral CA1 as compared with that in the ventral part of the CA1, in CA2, and in CA3 ipsilateral to the Aβ-injected side. The analysis also revealed a significant decrease in α7nAChR-immunoreactivity in the dentate gyrus ipsilateral to the Aβ-injected side as compared to the corresponding hemisphere of non-treated control animals and with that in the PBS-injected side co-localization studies showed that the α7nAChR protein is highly localized in GABA- and Parv-immunoreactive cells, while only few Calb-positive cells expressed immunoreactivity for α7nAChR. In addition, injections of Aβ protein resulted in a significant reduction in the number of GABA- and Parv-immunoreactive cells in the dorsal part of the ipsilateral CA1 as compared to the corresponding region of non-treated control animals and with that in the corresponding region of the PBS-injected side. Our findings suggest that Aβ induces a reduction in α7nAChR-containing cells, which may contribute to impairment of GABAergic synaptic transmission in the hippocampus.