Evidence map›Paper›PMID 27671323›Full record

ArticleNeuropharmacology2017

The antidepressant bupropion is a negative allosteric modulator of serotonin type 3A receptors.

Akash Pandhare, Aneesh Satya Pappu, Henrik Wilms, Michael Paul Blanton, Michaela Jansen

Abstract read
In one paragraph

Article in Neuropharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  7. Identification of a binding site for bupropion inbioRxiv : the preprint server for biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Akash PandhareDepartment of Cell Physiology and Molecular Biophysics, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Center for Membrane Protein Research, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA. Electronic address: akash.pandhare@ttuhsc.edu.
Aneesh Satya PappuDepartment of Cell Physiology and Molecular Biophysics, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA; The Clark Scholar Program, Texas Tech University, Lubbock, TX 79409, USA. Electronic address: apappu@standford.edu.
Henrik WilmsDepartment of Neurology, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA. Electronic address: henrik.wilms@ttuhsc.edu.
Michael Paul BlantonCenter for Membrane Protein Research, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA; Department of Pharmacology and Neuroscience, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA. Electronic address: michael.blanton@ttuhsc.edu.
Michaela JansenDepartment of Cell Physiology and Molecular Biophysics, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Center for Membrane Protein Research, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA. Electronic address: michaela.jansen@ttuhsc.edu.
Texas Tech University · US

Funding

Probing the structure and function of the intracellular domain of cys-loop receptorsR01NS077114 · NINDS · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI JANSEN, MICHAELA · 2014 to 2025
$3.1M
NINDS NIH HHS R01 NS077114
6 · The paper itself

Abstract

The FDA-approved antidepressant and smoking cessation drug bupropion is known to inhibit dopamine and norepinephrine reuptake transporters, as well as nicotinic acetylcholine receptors (nAChRs) which are cation-conducting members of the Cys-loop superfamily of ion channels, and more broadly pentameric ligand-gated ion channels (pLGICs). In the present study, we examined the ability of bupropion and its primary metabolite hydroxybupropion to block the function of cation-selective serotonin type 3A receptors (5-HT

Indexed as

Allosteric RegulationAnimalsAntidepressive Agents, Second-GenerationBupropionDose-Response Relationship, DrugGranisetronHEK293 CellsHumansMiceOocytesReceptors, Serotonin, 5-HT3SerotoninSerotonin 5-HT3 Receptor AntagonistsXenopus laevisAntidepressive Agents, Second-GenerationBupropionGranisetronHtr3a protein, mousehydroxybupropionReceptors, Serotonin, 5-HT3SerotoninSerotonin 5-HT3 Receptor Antagonists5-HT(3A) receptorsAntidepressantBupropionHydroxybupropionPentameric ligand-gated ion channels

Identifiers

PMID27671323
PMCPMC5148637
OpenAlexW2522264949

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.