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Emerging Alzheimer's disease therapies: focusing on the future

期刊

NEUROBIOLOGY OF AGING
卷 23, 期 6, 页码 985-990

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ELSEVIER SCIENCE INC
DOI: 10.1016/S0197-4580(02)00123-9

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neurodegenerative diseases; A beta; brain amyloidosis; drug discovery

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The Center for Neurodegenerative Disease Research (CNDR) organized a 1 day symposium entitled Emerging Alzheimer's disease Therapies: Focusing On The Future on November 7th, 2001 at the University of Pennsylvania in Philadelphia, PA. The agenda (Fig. 1) focused on novel therapies for Alzheimer's disease (AD) designed to prevent/eliminate Abeta deposits in the brains of AD patients. While fibrillar Abeta deposits known as senile plaques (SPs) and intraneuronal tau fibrils known as neurofibrillary tangles (NFTs) are diagnostic of AD, >50% of patients with familial or sporadic AD as well as elderly Down's syndrome patients with AD harbor a third type of brain amyloid known as Lewy bodies formed by intraneuronal alpha-synuclein fibrils [1,6]. Thus, AD is a triple brain amyloidosis since three different proteins (tau, alpha-synuclein) or peptide fragments (Abeta) of a larger Abeta precursor protein (APP) fibrillize and aggregate into pathological deposits of amyloid within (NFTs, LBs) and outside (SPs) neurons in AD brains. The symposium is summarized here followed by reviews from symposium speakers who describe potential anti-Abeta therapies some of which are in clinical trials [2,3]. (C) 2002 Elsevier Science Inc. All rights reserved.

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