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Pharmacotherapy of Alzheimer's Disease: Current State and Future Perspectives

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F14%3A10227238" target="_blank" >RIV/00179906:_____/14:10227238 - isvavai.cz</a>

  • Alternative codes found

    RIV/60162694:G44__/14:43875252

  • Result on the web

    <a href="http://dx.doi.org/10.2174/9781608058228114060003" target="_blank" >http://dx.doi.org/10.2174/9781608058228114060003</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/9781608058228114060003" target="_blank" >10.2174/9781608058228114060003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Pharmacotherapy of Alzheimer's Disease: Current State and Future Perspectives

  • Original language description

    Alzheimer's disease (AD) is a multifactorial disorder and apparently involves several different etiopathogenetic mechanisms. Up-to-date, there are no curative treatments or effective disease modifying therapies for AD. A strategy to enhance the cholinergic transmission by using acetylcholinesterase inhibitors (AChEIs) has been proposed more than two decades ago. Food and Drug Administration (FDA) gradually marketed these AChEIs: tacrine (1993), donepezil (1997), rivastigmine (2000) and galantamine (2001); tacrine is no longer used because of its high prevalence of hepatotoxicity. In addition to the AD cholinergic hypothesis , there is great evidence that voltage-gated, uncompetitive, N-methyl-D-aspartate (NMDA) antagonist memantine with moderate affinity can protect neurons from excitotoxicity. It was approved by FDA for treatment of moderate to severe stages of AD in 2003. Beyond symptomatic approaches there are anti-amyloid, neuroprotective and neuron-restorative strategies that hold

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    O - Projekt operacniho programu

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Book/collection name

    Frontiers in Drug Design &amp; Discovery. Volume 6

  • ISBN

    978-1-60805-822-8

  • Number of pages of the result

    37

  • Pages from-to

    702-738

  • Number of pages of the book

    766

  • Publisher name

    Bentham Science

  • Place of publication

    Neuveden

  • UT code for WoS chapter