Medicinal Chemistry of 5-HT5A Receptor Ligands: A Receptor Subtype with Unique Therapeutical Potential

Author(s): Balazs Volk , Bence J. Nagy , Szilvia Vas , Diana Kostyalik , Gyula Simig , Gyorgy Bagdy .

Journal Name: Current Topics in Medicinal Chemistry

Volume 10 , Issue 5 , 2010

Become EABM
Become Reviewer

Abstract:

Although the 5-HT5 receptor subfamily was discovered more than 15 years ago, it is unambiguously the least known 5-HT receptor subtype. The Gi/G0-mediated signal transduction and its intensive presence in raphe and other brainstem and pons nuclei suggest mechanisms similar to those of 5-HT1 receptors, the ligands of which are already applied in the treatment of e.g. anxiety and migraine. In addition, a unique coupling and inhibition of adenosine diphosphate-ribosyl cyclase have also been described. High concentrations of 5-HT5 receptor in other key regions including, e.g. locus coeruleus, nucleus of the solitary tract, arcuate and suprachiasmatic nuclei of the hypothalamus indicate a wide range of physiological effects, thus its ligands are potential drug candidates in various areas, e.g. anxiety, sleep, incontinence, food intake, learning and memory, pain or chemoreception pathways. These findings have motivated several institutes and pharmaceutical companies to participate in the research of this field. Despite extensive research, no selective agonist and only two selective antagonists have been identified until now. Beyond these compounds, the present review provides a complete overview on all other published 5-HT5A receptor ligands as well as on the structure, function, distribution, genetics and possible therapeutic applications of this receptor.

Keywords: Serotonin, 5-HT5, 5-HT5A, 5-HT autoreceptor, neuronal hyperpolarization, drug target, anxiety, sleep, incontinence, food intake, learning and memory, pain

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 10
ISSUE: 5
Year: 2010
Page: [554 - 578]
Pages: 25
DOI: 10.2174/156802610791111588
Price: $58

Article Metrics

PDF: 24