Evidence map›Paper›PMID 32487753›Full record

ArticlemBio2020

Chlorpromazine and Amitriptyline Are Substrates and Inhibitors of the AcrB Multidrug Efflux Pump.

Elizabeth M Grimsey, Chiara Fais, Robert L Marshall, Vito Ricci, Maria Laura Ciusa, Jack W Stone, Alasdair Ivens, Giuliano Malloci, Paolo Ruggerone, Attilio V Vargiu and 1 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 83 citations in OpenAlex.

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  8. Broadly Defined Antibiotic Adjuvants forThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
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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

11 authors at 3 institutions in 3 countries.

Elizabeth M GrimseyAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0003-1211-2598
Chiara FaisDepartment of Physics, University of Cagliari, Monserrato, Italy.
Robert L MarshallAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom.
Vito RicciAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom.
Maria Laura CiusaAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom.
Jack W StoneAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom.
Alasdair IvensCentre for Immunity, Infection and Evolution, University of Edinburgh Ashworth Labs, Edinburgh, United Kingdom.
Giuliano MallociDepartment of Physics, University of Cagliari, Monserrato, Italy.
Paolo RuggeroneDepartment of Physics, University of Cagliari, Monserrato, Italy.
Attilio V VargiuDepartment of Physics, University of Cagliari, Monserrato, Italy vargiu@dsf.unica.it L.J.V.PIDDOCK@bham.ac.uk.ORCID 0000-0003-4013-8867
Laura J V PiddockAntimicrobials Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, Institute of Microbiology and Infection, The University of Birmingham, Birmingham, United Kingdom vargiu@dsf.unica.it L.J.V.PIDDOCK@bham.ac.uk.ORCID 0000-0003-1460-473X
University of Birmingham · GBUniversity of Cagliari · ITCentre for Immunity, Infection and Evolution · GB

Funding

Optimization of efflux avoidance and inhibition for antibiotic developmentR01AI136799 · NIAID · UNIVERSITY OF OKLAHOMA · PI GNANAKARAN, SANDRASEGARAM, RUGGERONE, PAOLO · 2018 to 2022
$5.7M
Medical Research Council MR/N017846/1Medical Research Council MR/P022596/1NIAID NIH HHS R01 AI136799
6 · The paper itself

Abstract

Efflux is an important mechanism in Gram-negative bacteria conferring multidrug resistance. Inhibition of efflux is an encouraging strategy to restore the antibacterial activity of antibiotics. Chlorpromazine and amitriptyline have been shown to behave as efflux inhibitors. However, their mode of action is poorly understood. Exposure of

Indexed as

AmitriptylineAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsChlorpromazineDrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli ProteinsMembrane Transport ProteinsMicrobial Sensitivity TestsMolecular Docking SimulationMutationProtein BindingSalmonella entericaAcrB protein, E coliAcrB protein, Salmonella entericaAmitriptylineAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsChlorpromazineEscherichia coli ProteinsMembrane Transport ProteinsAcrBantibiotic resistanceantipsychotic drugsefflux pump inhibitorsefflux pumps

Identifiers

PMID32487753
PMCPMC7267879
OpenAlexW3032054954

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.