Journal Article

Metal Ionophore Treatment Restores Dendritic Spine Density and Synaptic Protein Levels in a Mouse Model of Alzheimer's Disease

Nurjono, Milawaty, Filiz, Gulay, Crouch, Peter J., Finkelstein, David I., White, Anthony R., Donnelly, Paul S., Bush, Ashley I., Adlard, Paul A., Cappai, Roberto, Bica, Laura

2011

نظرة عامة

We have previously demonstrated that brief treatment of APP transgenic mice with metal ionophores (PBT2, Prana Biotechnology) rapidly and markedly improves learning and memory. To understand the potential mechanisms of action underlying this phenomenon we examined hippocampal dendritic spine density, and the levels of key proteins involved in learning and memory, in young (4 months) and old (14 months) female Tg2576 mice following brief (11 days) oral treatment with PBT2 (30 mg/kg/d). Transgenic mice exhibited deficits in spine density compared to littermate controls that were significantly rescued by PBT2 treatment in both the young (+17%, p<0.001) and old (+32%, p<0.001) animals. There was no effect of PBT2 on spine density in the control animals. In the transgenic animals, PBT2 treatment also resulted in significant increases in brain levels of CamKII (+57%, p = 0.005), spinophilin (+37%, p = 0.04), NMDAR1A (+126%, p = 0.02), NMDAR2A (+70%, p = 0.05), pro-BDNF (+19%, p = 0.02) and BDNF (+19%, p = 0.04). While PBT2-treatment did not significantly alter neurite-length in vivo, it did increase neurite outgrowth (+200%, p = 0.006) in cultured cells, and this was abolished by co-incubation with the transition metal chelator, diamsar. These data suggest that PBT2 may affect multiple aspects of snaptic health/efficacy. In Alzheimer's disease therefore, PBT2 may restore the uptake of physiological metal ions trapped within extracellular β-amyloid aggregates that then induce biochemical and anatomical changes to improve cognitive function.

• الناشر: Public Library of Science,Public Library of Science (PLoS)
• موضوع: Alzheimer Disease - metabolism / Alzheimer Disease - pathology / Alzheimer's disease / Animal cognition / Animal genetic engineering / Animals / Axonogenesis / Biology / Biotechnology / Brain / Brain research / Brain-derived neurotrophic factor / Ca2+/calmodulin-dependent protein kinase II / Cell culture / Cells, Cultured / Clinical trials / Clioquinol - analogs & derivatives / Cognitive ability / Dendritic spines / Dendritic Spines - drug effects / Dendritic Spines - pathology / Density / Disease Models, Animal / Drug dosages / Female / Genetically modified animals / Glutamate receptors / Glutamic acid receptors / Hippocampus / Hippocampus - drug effects / Hippocampus - pathology / Ionophores / Ionophores - administration & dosage / Ionophores - pharmacology / Kinases / Laboratories / Learning / Medical research / Medical treatment / Memory / Memory - drug effects / Mental health / Metals / Metals - administration & dosage / Metals - pharmacology / Mice / Mice, Transgenic / Morphology / N-Methyl-D-aspartic acid receptors / Nerve Tissue Proteins - metabolism / Neurites - drug effects / Neurites - metabolism / Neurobiology / Neurodegenerative diseases / Neurogenesis - drug effects / Neurons / Neurosciences / Oxidation / Pathology / Physiological aspects / Potassium / Proteins / Rodents / Spine / Spinophilin / Synapses - metabolism / Synaptic density / Transgenic animals / Transgenic mice / Trends / Zinc / β-Amyloid