Literature DB >> 16273026

Rationalizing therapeutic approaches in Alzheimer's disease.

George T Grossberg1.   

Abstract

Deficits in cholinergic and glutamatergic neurotransmission have been linked to the symptomatology of Alzheimer's disease, and current therapies for Alzheimer's, including cholinesterase inhibitors (ChEIs) and the N-methyl-d-aspartate receptor antagonist memantine, have been developed to compensate for these deficits. This article reviews the results of clinical trials involving agents approved by the United States Food and Drug Administration for use in the treatment of Alzheimer's disease (namely, ChEIs for mild to moderate Alzheimer's and memantine for moderate to severe Alzheimer's). In particular, the efficacy of current monotherapy strategies in the treatment of cognitive and functional symptoms of Alzheimer's disease will be addressed. In addition, data from a clinical trial examining the use of a ChEI in combination with memantine will also be discussed, as it has been hypothesized that ChEIs and memantine may offer synergistic benefits due to their distinct mechanisms of action.

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Year:  2005        PMID: 16273026     DOI: 10.1017/s109285290001419x

Source DB:  PubMed          Journal:  CNS Spectr        ISSN: 1092-8529            Impact factor:   3.790


  3 in total

Review 1.  N-methyl D-aspartate (NMDA) receptor antagonists and memantine treatment for Alzheimer's disease, vascular dementia and Parkinson's disease.

Authors:  David Olivares; Varun K Deshpande; Ying Shi; Debomoy K Lahiri; Nigel H Greig; Jack T Rogers; Xudong Huang
Journal:  Curr Alzheimer Res       Date:  2012-07       Impact factor: 3.498

2.  PMS777, a new cholinesterase inhibitor with anti-platelet activated factor activity, regulates amyloid precursor protein processing in vitro.

Authors:  Hong-Qi Yang; Zhi-Kun Sun; Yan-Xin Zhao; Jing Pan; Mao-Wen Ba; Guo-Qiang Lu; Jian-Qing Ding; Hong-Zhuan Chen; Sheng-Di Chen
Journal:  Neurochem Res       Date:  2008-08-29       Impact factor: 3.996

3.  NMDA receptors mediate synaptic depression, but not spine loss in the dentate gyrus of adult amyloid Beta (Aβ) overexpressing mice.

Authors:  Michaela Kerstin Müller; Eric Jacobi; Kenji Sakimura; Roberto Malinow; Jakob von Engelhardt
Journal:  Acta Neuropathol Commun       Date:  2018-10-23       Impact factor: 7.801

  3 in total

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