Literature DB >> 23891641

Therapeutics of Alzheimer's disease: Past, present and future.

R Anand1, Kiran Dip Gill, Abbas Ali Mahdi.   

Abstract

Alzheimer's disease (AD) is the most common cause of dementia worldwide. The etiology is multifactorial, and pathophysiology of the disease is complex. Data indicate an exponential rise in the number of cases of AD, emphasizing the need for developing an effective treatment. AD also imposes tremendous emotional and financial burden to the patient's family and community. The disease has been studied over a century, but acetylcholinesterase inhibitors and memantine are the only drugs currently approved for its management. These drugs provide symptomatic improvement alone but do less to modify the disease process. The extensive insight into the molecular and cellular pathomechanism in AD over the past few decades has provided us significant progress in the understanding of the disease. A number of novel strategies that seek to modify the disease process have been developed. The major developments in this direction are the amyloid and tau based therapeutics, which could hold the key to treatment of AD in the near future. Several putative drugs have been thoroughly investigated in preclinical studies, but many of them have failed to produce results in the clinical scenario; therefore it is only prudent that lessons be learnt from the past mistakes. The current rationales and targets evaluated for therapeutic benefit in AD are reviewed in this article. This article is part of the Special Issue entitled 'The Synaptic Basis of Neurodegenerative Disorders'.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Alzheimer's disease; Amyloid; Dementia; Neurofibrillary tangles; Neuropharmacology

Mesh:

Substances:

Year:  2013        PMID: 23891641     DOI: 10.1016/j.neuropharm.2013.07.004

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  169 in total

Review 1.  Poor Gait Performance and Prediction of Dementia: Results From a Meta-Analysis.

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2.  Vildagliptine protects SH-SY5Y human neuron-like cells from Aβ 1-42 induced toxicity, in vitro.

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3.  Exploration of the Acetylcholinesterase Inhibitory Activity of Some Alkaloids from Amaryllidaceae Family by Molecular Docking In Silico.

Authors:  Willian O Castillo-Ordóñez; Elvira R Tamarozzi; Gabriel M da Silva; Andrés F Aristizabal-Pachón; Elza T Sakamoto-Hojo; Catarina S Takahashi; Silvana Giuliatti
Journal:  Neurochem Res       Date:  2017-05-11       Impact factor: 3.996

4.  Aβ-Mediated Dysregulation of F-Actin Nanoarchitecture Leads to Loss of Dendritic Spines and Alzheimer's Disease-Related Cognitive Impairments.

Authors:  Hossein Sanjari Moghaddam; Mohammad Hadi Aarabi
Journal:  J Neurosci       Date:  2018-06-27       Impact factor: 6.167

5.  Imidazo[2,1]thiazol-3-one Derivatives Useful as Diagnostic Agents for Alzheimer's Disease.

Authors:  Benjamin Blass
Journal:  ACS Med Chem Lett       Date:  2014-04-28       Impact factor: 4.345

6.  Early Preclinical Changes in Hippocampal CREB-Binding Protein Expression in a Mouse Model of Familial Alzheimer's Disease.

Authors:  Miren Ettcheto; Sonia Abad; Dmitry Petrov; Ignacio Pedrós; Oriol Busquets; Elena Sánchez-López; Gemma Casadesús; Carlos Beas-Zarate; Eva Carro; Carme Auladell; Jordi Olloquequi; Merce Pallàs; Jaume Folch; Antoni Camins
Journal:  Mol Neurobiol       Date:  2017-07-27       Impact factor: 5.590

Review 7.  An overview on therapeutics attenuating amyloid β level in Alzheimer's disease: targeting neurotransmission, inflammation, oxidative stress and enhanced cholesterol levels.

Authors:  Xiaoling Zhou; Yifei Li; Xiaozhe Shi; Chun Ma
Journal:  Am J Transl Res       Date:  2016-02-15       Impact factor: 4.060

Review 8.  Alzheimer's Disease Therapeutic Approaches.

Authors:  Maria Revi
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

Review 9.  Stroke, Vascular Dementia, and Alzheimer's Disease: Molecular Links.

Authors:  Murali Vijayan; P Hemachandra Reddy
Journal:  J Alzheimers Dis       Date:  2016-09-06       Impact factor: 4.472

Review 10.  Amyloid-Beta and Phosphorylated Tau Accumulations Cause Abnormalities at Synapses of Alzheimer's disease Neurons.

Authors:  Ravi Rajmohan; P Hemachandra Reddy
Journal:  J Alzheimers Dis       Date:  2017       Impact factor: 4.472

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