Research

C3-halogenation of cytisine generates potent and efficacious nicotinic receptor agonists


Reference:

Abin-Carriquiry, J. A., Voutilainen, M. H., Barik, J., Cassels, B. K., Iturriaga-Vasquez, P., Bermudez, I., Durand, C., Dajas, F. and Wonnacott, S., 2006. C3-halogenation of cytisine generates potent and efficacious nicotinic receptor agonists. European Journal of Pharmacology, 536 (1-2), pp. 1-11.

Related documents:

This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below.

Official URL:

http://dx.doi.org/10.1016/j.ejphar.2006.02.012

Abstract

Neuronal nicotinic acetylcholine receptors subserve predominantly modulatory roles in the brain, making them attractive therapeutic targets. Natural products provide key leads in the quest for nicotinic receptor subtype-selective compounds. Cytisine, found in Leguminosae spp., binds with high affinity to alpha 4 beta 2* nicotinic receptors. We have compared the effect of C3 and C5 halogenation of cytisine and methylcytisine (MCy) on their interaction with native rat nicotinic receptors. 3-Bromocytisine (3-BrCy) and 3-iodocytisine (3-ICy) exhibited increased binding affinity (especially at alpha 7 nicotinic receptors; K-1 similar to 0.1 mu M) and functional potency, whereas C5-halogenation was detrimental. 3-BrCy and 3-ICy were more potent than cytisine at evoking [H-3]dopamine release from striatal slices (EC50 similar to 11 nM), [H-3]noradrenaline release from hippocampal slices (EC50 similar to 250 nM), increases in intracellular Ca2+ in PC12 cells and inward currents in Xenopus oocytes expressing human alpha 3 beta 4 4 nicotinic receptor (EC50 similar to 2 mu M). These compounds were also more efficacious than cytisine. C3-halogenation of cytisine is proposed to stabilize the open conformation of the nicotinic receptor but does not enhance subtype selectivity.

Details

Item Type Articles
CreatorsAbin-Carriquiry, J. A., Voutilainen, M. H., Barik, J., Cassels, B. K., Iturriaga-Vasquez, P., Bermudez, I., Durand, C., Dajas, F. and Wonnacott, S.
DOI10.1016/j.ejphar.2006.02.012
DepartmentsFaculty of Science > Biology & Biochemistry
RefereedYes
StatusPublished
ID Code3739

Export

Actions (login required)

View Item