Endogenous secreted amyloid precursor protein-alpha regulates hippocampal NMDA receptor function, lo
July 3rd, 2008 | by admin |Endogenous secreted amyloid precursor protein-alpha regulates hippocampal NMDA receptor function, long-term potentiation and spatial memory.
Secreted amyloid precursor protein-alpha (sAPPalpha) levels are reduced during the pathogenesis of Alzheimer\’s disease, but the significance of this for neural function is not well understood. Here, we show that intrahippocampal infusion of antibodies targeted to endogenous sAPPalpha reduced long-term potentiation (LTP) in the dentate gyrus of adult rats by approximately 50%. Conversely, infusion of recombinant sAPPalpha dose-dependently increased LTP and facilitated in vitro tetanically evoked NMDA receptor-mediated currents. Pharmacological inhibition of alpha-secretase and other a-disintegrin-and-metalloproteases by TAPI-1 reduced both LTP and tetanus-evoked NMDA receptor-mediated currents in dentate granule cells. Both effects were prevented by co-application of exogenous recombinant sAPPalpha. Similarly, spatial memory was inhibited by intrahippocampal TAPI-1, an effect that was prevented by co-application of recombinant sAPPalpha. Together these findings indicate that endogenous sAPPalpha is a key contributor to synaptic plasticity and spatial memory. Its reduced production in Alzheimer\’s disease may thus contribute to the clinical memory deficits.
Taylor CJ, Ireland DR, Ballagh I, Bourne K, Marechal NM, Turner PR, Bilkey DK, Tate WP, Abraham WC.
Department of Psychology, University of Otago, Box 56, Dunedin, New Zealand.