Author:
Derijks Hieronymus J.,Heerdink Eibert R.,Janknegt Rob,Koning Fred H.P. De,Olivier Berend,Loonen Anton J.M.,Egberts Antoine C.G.
Abstract
Antidepressants have different receptor binding profiles, which are related to therapeutic action and adverse
drug reactions. We constructed a model to classify antidepressants on the basis of their binding properties of most common
transporter- and receptor sites. Receptor binding was quantified by calculating receptor occupancy for the 5-HT
(serotonin) reuptake transporter, norepinephrinic reuptake transporter, 5-HT2C-receptor, M3-receptor, H1-receptor and 1-
receptor. To identify groups of antidepressants that show similar patterns of receptor occupancy for different receptors,
hierarchical cluster analysis (HCA) and principle component analysis (PCA) were used. In addition, to visualize
(a)symmetry between binding profiles of antidepressants, radar plots were constructed. On the basis of both analyses, four
clusters of antidepressants which exert similar pharmacological properties were identified. Potentially, this model could
be a helpful tool in medical practice and may be used as a prediction model for adverse effects of drugs entering the market.
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine
Cited by
24 articles.
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