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Small-molecule modulation of neurotrophin receptors: a strategy for the treatment of neurological disease

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NATURE REVIEWS DRUG DISCOVERY
卷 12, 期 7, 页码 507-525

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NATURE PUBLISHING GROUP
DOI: 10.1038/nrd4024

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资金

  1. NIA [UO1 AG032225]
  2. Alzheimer's Drug Discovery Foundation
  3. Alzheimer's Association
  4. Eastern Chapter of the North Carolina Alzheimer's Association
  5. Koret Foundation
  6. Taube Philanthropies
  7. Jean Perkins Foundation
  8. Horngren Family Alzheimer's Research Fund
  9. Richard M. Lucas Foundation
  10. US Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development

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Neurotrophins and their receptors modulate multiple signalling pathways to regulate neuronal survival and to maintain axonal and dendritic networks and synaptic plasticity. Neurotrophins have potential for the treatment of neurological diseases. However, their therapeutic application has been limited owing to their poor plasma stability, restricted nervous system penetration and, importantly, the pleiotropic actions that derive from their concomitant binding to multiple receptors. One strategy to overcome these limitations is to target individual neurotrophin receptors-such as tropomyosin receptor kinase A (TRKA), TRKB, TRKC, the p75 neurotrophin receptor or sortilin-with small-molecule ligands. Such small molecules might also modulate various aspects of these signalling pathways in ways that are distinct from the programmes triggered by native neurotrophins. By departing from conventional neurotrophin signalling, these ligands might provide novel therapeutic options for a broad range of neurological indications.

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