4.7 Article

Withanamides in Withania somnifera Fruit Protect PC-12 Cells from β-Amyloid Responsible for Alzheimer's Disease

Journal

PHYTOTHERAPY RESEARCH
Volume 24, Issue 6, Pages 859-863

Publisher

WILEY
DOI: 10.1002/ptr.3033

Keywords

Aswagandha; beta-amyloid peptide; neuronal cells; lipid peroxidation; molecular models

Funding

  1. Natural Therapeutics, Llc., Michigan

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Alzheimer's disease (AD) is an irreversible neurodegenerative disorder with symptoms of confusion, memory loss, and mood swings. The beta-amyloid peptide, with 39-42 amino acid residues (BAP), plays a significant role in the development of AD. Although there is no cure for AD, it can be managed with available drugs to some degree. Several studies have revealed that natural antioxidants, such as vitamin E, vitamin C and beta-carotene, may help in scavenging free radicals generated during the initiation and progression of this disease. Therefore, there has been considerable interest in plant phytochemicals with antioxidant property as potential agents to prevent the progression of AD. Our earlier investigations of the Withania somnifera fruit afforded lipid per. oxidation inhibitory withanamides that are more potent than the commercial antioxidants. In this study, we have tested two major withanamides A (WA) and C (WC) for their ability to protect the PC-12 cells, rat neuronal cells, from P-amyloid induced cell damage. The cell death caused by beta-amyloid was negated by withanamide treatment. Molecular modeling studies showed that withanamides A and C uniquely bind to the active motif of beta-amyloid (25-35) and suggest that withanamides have the ability to prevent the fibril formation. Further understanding of the mechanism of action and in vivo efficacy of these withanamides may facilitate its development as a prophylaxis. Copyright (C) 2009 John Wiley & Sons, Ltd.

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