Evidence map›Paper›PMID 30048457›Full record

ArticlePLoS biology2018

Bile diversion, a bariatric surgery, and bile acid signaling reduce central cocaine reward.

India A Reddy, Nicholas K Smith, Kevin Erreger, Dipanwita Ghose, Christine Saunders, Daniel J Foster, Brandon Turner, Amanda Poe, Vance L Albaugh, Owen McGuinness and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  10. Mucosal and hormonal adaptations after Roux-en-Y gastric bypass.Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery · 2023
    Review
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  12. Obesity - A Matter of Motivation?Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association · 2022
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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

15 authors at 3 institutions in 1 country.

India A ReddyNeuroscience Program, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Nicholas K SmithNeuroscience Program, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Kevin ErregerDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Dipanwita GhoseDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Christine SaundersDepartment of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Daniel J FosterDepartment of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Brandon TurnerNeuroscience Program, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Amanda PoeDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Vance L AlbaughDepartment of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Owen McGuinnessDepartment of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Troy A HackettDepartment of Hearing and Speech Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Brad A GrueterDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Naji N AbumradDepartment of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Charles Robb FlynnDepartment of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Aurelio GalliDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID 0000-0001-7173-9345
Vanderbilt University Medical Center · USVanderbilt University · USUniversity of Alabama at Birmingham · US

Funding

University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARRELL, FRANK E. · 2015 to 2019
$7.1M
The Role of the Dopamine Transporter in Psychostimulant AbuseR01DA038058 · NIDA · VANDERBILT UNIVERSITY · PI GALLI, AURELIO, MATTHIES, HEINRICH J.G. · 2014 to 2025
$4.6M
Bile Diversion: A Simple and Effective Method of Treating ObesityR01DK105847 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ABUMRAD, NAJI N, FLYNN, CHARLES R · 2015 to 2019
$1.8M
Identification of Cellular Phenotypes in the Auditory ForebrainR01DC015388 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HACKETT, TROY A. · 2016 to 2020
$1.7M
Bile acid signaling as a pharmacological target for the treatment of cocaine abuseR21DA043960 · NIDA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FLYNN, CHARLES R, GALLI, AURELIO · 2018 to 2019
$383k
GPU-Accelerated Parallel Computer for Drug Discovery ApplicationsS10OD020154 · OD · VANDERBILT UNIVERSITY · PI SMITH, JARROD ANSON · 2015 to 2015
$225k
NICHD NIH HHS U54 HD083211NIDA NIH HHS R01 DA038058NIDA NIH HHS R21 DA043960NIDCD NIH HHS R01 DC015388NIDDK NIH HHS P30 DK079626NIDDK NIH HHS R01 DK105847
6 · The paper itself

Abstract

The gut-to-brain axis exhibits significant control over motivated behavior. However, mechanisms supporting this communication are poorly understood. We reveal that a gut-based bariatric surgery chronically elevates systemic bile acids and attenuates cocaine-induced elevations in accumbal dopamine. Notably, this surgery reduces reward-related behavior and psychomotor sensitization to cocaine. Utilizing a knockout mouse model, we have determined that a main mediator of these post-operative effects is the Takeda G protein-coupled bile acid receptor (TGR5). Viral restoration of TGR5 in the nucleus accumbens of TGR5 knockout animals is sufficient to restore cocaine reward, centrally localizing this TGR5-mediated modulation. These findings define TGR5 and bile acid signaling as pharmacological targets for the treatment of cocaine abuse and reveal a novel mechanism of gut-to-brain communication.

Indexed as

Bariatric SurgeryRewardSignal TransductionAnimalsBehavior, AnimalBileChoice BehaviorCocaineDopamineGallbladderIleumMaleMice, Inbred C57BLMice, KnockoutMotor ActivityNucleus AccumbensCocaineDopamine

Identifiers

PMID30048457
PMCPMC6061973
OpenAlexW2884079431

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.