The research proposed in this application is to identify a novel drug candidate for the treatment of Alzheimer's disease (AD). AD is the largest neurodegenerative disease, afflicting ~4.5 million Americans and having total societal costs associated with the disease of about $100 billion per year. Incidence and costs of this disease are projected to grow substantially in the coming decades and there is no currently approved therapy that is truly effective. Current therapies are considered to be palliative, directed towards disease symptoms, and their efficacy is typically of limited duration, slowing the progression of the disease by several months. In this project we will identify the active component of a botanical extract that has been shown to selectively lower the concentration of amyloid beta peptide 1-42 (A042, "long A-beta") Deposition of Ap42 is an early and ubiquitous feature of AD. Ap42 is less soluble and more toxic than the primary form of Ap, the two residue shorter form Ap40. Genetic mutations in the precursor protein of Ap, and in the enzymes that process it to produce Ap, that are associated with early-onset AD increase Ap42 levels. Lowering Ap42 selectively is expected to substantially lower the amyloid-forming potential of the total Ap pool, slow the growth of amyloid deposits, retard the transformation of diffuse amyloid plaques to the compact dense senile amyloid plaques associated with disease, and inhibit the formation of toxic oligomers of Ap associated with acute toxicity to neurons. The Ap42 lowering activity of interest in this proposal is derived from the flowering plant actaea racemosa. This plant, also known as black cohosh, is the source of an extract that is widely used as a nutriceutical for the treatment of menopausal symptoms in women. Preliminary data suggest that the Ap42 lowering activity is separate from the triterpenes associated with the conventional use of this extract. In phase one of this project we will use cell-based assays of AP40/42 expression to guide fractionation of actaea racemosa extract and isolate substantially enriched samples of the Ap42 lowering activity. In phase two of this project, the active component of the extract will be purified to homogeneity, its structure will be determined and preliminary efficacy and pharmacology studies will be performed in mice. This compound will be of interest for other neurological disorders where Ap-related toxicity may be a contributing factor.
Thesaurus Terms: Alzheimer's disease, amyloid protein, chemical structure function, drug discovery /isolation, plant extract gene expression, neuritic plaque, pathologic process gel filtration chromatography, mass spectrometry, nuclear magnetic resonance spectroscopy, subcellular fractionation
