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Agonists and antagonists induce different palonosetron dissociation rates in 5-HT(3)A and 5-HT(3)AB receptors()

Palonosetron is a potent 5-HT(3) receptor antagonist with a unique structure and some unusual properties. Here we explore the properties of palonosetron at heterologously expressed 5-HT(3)A and 5-HT(3)AB receptors. We used receptors expressed in HEK293 cells, and functionally analysed them using a m...

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Detalles Bibliográficos
Autores principales: Lummis, Sarah C.R., Thompson, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778450/
https://www.ncbi.nlm.nih.gov/pubmed/23747573
http://dx.doi.org/10.1016/j.neuropharm.2013.05.010
Descripción
Sumario:Palonosetron is a potent 5-HT(3) receptor antagonist with a unique structure and some unusual properties. Here we explore the properties of palonosetron at heterologously expressed 5-HT(3)A and 5-HT(3)AB receptors. We used receptors expressed in HEK293 cells, and functionally analysed them using a membrane potential sensitive dye in a Flexstation, which revealed IC(50)s of 0.24 nM and 0.18 nM for 5-HT(3)A and 5-HT(3)AB receptors respectively. Radioligand binding studies with [(3)H]palonosetron revealed similar K(d)s: 0.34 nM for 5-HT(3)A and 0.15 nM for 5-HT(3)AB receptors. Kinetic studies showed palonosetron association and dissociation rates were slightly faster in 5-HT(3)AB than 5-HT(3)A receptors, and for both subtypes dissociation rates were ligand-dependent, with antagonists causing more rapid dissociation than agonists. Similar ligand effects were not observed for [(3)H]granisetron dissociation studies. These data support previous studies which show palonosetron has actions distinct to other 5-HT(3) receptor antagonists, and the slow rates observed for agonist induced dissociation (t(1/2) > 10 h) could at least partly explain the long duration of palonosetron effects in vivo.