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Current Alzheimer Research

Volume 7 Issue 3
ISSN: 1567-2050
eISSN: 1875-5828


   All Titles

  Fragile X Syndrome and Alzheimer's Disease: Another Story About APP and β -Amyloid
  pp.200-206 (7) Authors: J.S. Malter, B.C. Ray, P.R. Westmark, C.J. Westmark

As the mechanisms underlying neuronal development and degeneration become clarified, a number of common effectors and signaling pathways are becoming apparent. Here we describe the identification of Aβ, long considered a pathologic mediator of Alzheimers Disease and Down Syndrome, as similarly over-expressed in the neurodevelopmental disease, Fragile X Syndrome. We also show that mGluR5 inhibitors, currently employed for the treatment of Fragile X, reduce Aβ production in rodent models of Fragile X and AD as well as reduce disease phenotypes including seizures. Thus seemingly disparate neurologic diseases may share a common pathologic instigator and be treatable with a common, currently available class of therapeutics.

  Keywords: Metabotropic glutamate receptors (mGluR), Fragile X Syndrome (FXS), amyloid precursor protein (APP), beta-amyloid
  Affiliation: R509T, Waisman Center, 1500 Highland Ave, Madison, WI 53705, USA.
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