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Molecular basis of atypicality of bupropion inferred from its receptor engagement in nervous system tissues.

Authors :
Kim EJ
Felsovalyi K
Young LM
Shmelkov SV
Grunebaum MF
Cardozo T
Source :
Psychopharmacology [Psychopharmacology (Berl)] 2018 Sep; Vol. 235 (9), pp. 2643-2650. Date of Electronic Publication: 2018 Jul 01.
Publication Year :
2018

Abstract

Despite decades of clinical use and research, the mechanism of action (MOA) of antidepressant medications remains poorly understood. Selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs) are the most commonly prescribed antidepressants-atypical antidepressants such as bupropion have also proven effective, while exhibiting a divergent clinical phenotype. The difference in phenotypic profiles presumably lies in the differences among the MOAs of SSRIs/SNRIs and bupropion. We integrated the ensemble of bupropion's affinities for all its receptors with the expression levels of those targets in nervous system tissues. This "combined target tissue" profile of bupropion was compared to those of duloxetine, fluoxetine, and venlafaxine to isolate the unique target tissue effects of bupropion. Our results suggest that the three monoamines-serotonin, norepinephrine, and dopamine-all contribute to the common antidepressant effects of SSRIs, SNRIs, and bupropion. At the same time, bupropion is unique in its action on 5-HT3AR in the dorsal root ganglion and nicotinic acetylcholine receptors in the pineal gland. These unique tissue-specific activities may explain unique therapeutic effects of bupropion, such as pain management and smoking cessation, and, given melatonin's association with nicotinic acetylcholine receptors and depression, highlight the underappreciated role of the melatonergic system in bupropion's MOA.

Details

Language :
English
ISSN :
1432-2072
Volume :
235
Issue :
9
Database :
MEDLINE
Journal :
Psychopharmacology
Publication Type :
Academic Journal
Accession number :
29961917
Full Text :
https://doi.org/10.1007/s00213-018-4958-9