Summary
December 2007, Vol. 7, No. 12, Pages 1853-1867 , DOI 10.1517/14712598.7.12.1853

Novel strategies for Alzheimer's disease treatment

Brian Spencer1, Research Associate, Edward Rockenstein1, Research Associate, Leslie Crews2, Graduate Student, Robert Marr3, Assistant Professor & Eliezer Masliah1,2, Professor
1University of California, Department of Neurosciences, San Diego, La Jolla, CA 92093-0624, USA
2University of California, Department of Pathology, San Diego, La Jolla, CA 92093, USA +1 858 534 8992; +1 858 534 6232;
3Rosalind Franklin University of Medicine and Science, Department of Neuroscience, North Chicago, Illinois, 60064, USA
Author for correspondence



Considerable progress has been made in recent years towards better understanding the pathogenesis of Alzheimer's disease (AD), a dementing neurodegenerative disorder that affects > 10 million individuals in the US and Europe combined. Recent studies suggest that alterations in the processing of amyloid precursor protein (APP), resulting in the accumulation of amyloid-β protein (Aβ) and the formation of oligomers leads to synaptic damage and neurodegeneration. Therefore, strategies for treatment development have been focused on reducing Aβ accumulation using, among other approaches, antiaggregation molecules, regulators of the APP proteolysis and processing, reducing APP production (e.g., small-interfering RNA), and increasing Aβ clearance with antibodies, apolipoprotein E and Aβ-degrading enzymes (e.g., neprilysin). The main focus of this review is on novel treatments for AD with a special emphasis on delivering neuroprotective and antiamyloidogenic molecules by gene therapy and by promoting neurogenesis.

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Authors:
Brian Spencer
Edward Rockenstein
Leslie Crews
Robert Marr
Eliezer Masliah
Keywords:
Alzheimer's disease
amyloid
apolipoprotein E
blood–brain barrier
cerebrolysin
gene therapy
neprilysin
plaques
siRNA
tangles
tau