A Perspective on Multi-target Drugs for Alzheimer's Disease
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
32448557
DOI
10.1016/j.tips.2020.04.008
PII: S0165-6147(20)30094-8
Knihovny.cz E-resources
- Keywords
- Alzheimer’s disease, designed multiple ligands, drug design, multi-target drugs, polypharmacology,
- MeSH
- Alzheimer Disease * drug therapy MeSH
- Pharmaceutical Preparations * MeSH
- Drug Delivery Systems MeSH
- Humans MeSH
- Synaptic Transmission MeSH
- Oxidative Stress MeSH
- Inflammation MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Pharmaceutical Preparations * MeSH
Alzheimer's disease (AD) has a complex pathophysiology that includes aggregation of pathological proteins, impaired neurotransmission, increased oxidative stress, or microglia-mediated neuroinflammation. Therapeutics targeting only one of these AD-related subpathologies have not yet been successful in the search for a disease-modifying treatment. Therefore, multi-target drugs (MTDs) aiming simultaneously at several subpathologies are expected to be a better approach. However, the concept of MTD is inherently connected with several limitations, which are often ignored during MTD design and development. Here, we provide an overview of the MTD approach and discuss its potential pitfalls in the context of AD treatment. We also put forward ideas to be used in the rational design of MTDs to obtain drugs that are effective against AD.
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