Evidence map›Paper›PMID 25628528›Full record

ReviewFrontiers in neuroscience2014

The 5-HT7 receptor as a potential target for treating drug and alcohol abuse.

Sheketha R Hauser, Peter B Hedlund, Amanda J Roberts, Youssef Sari, Richard L Bell, Eric A Engleman

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  8. Review
  9. Review
  10. Article
  11. Design and discovery of a high affinity, selective and β-arrestin biased 5-HTMedicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2022
    Article
  12. Article
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  14. Review
  15. Identification ofeLife · 2020
    Article
  16. Article
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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

6 authors at 4 institutions in 1 country.

Sheketha R HauserDepartment of Psychiatry, Indiana University School of Medicine Indianapolis, IN, USA.
Peter B HedlundDepartment of Molecular and Cellular Neuroscience, The Scripps Research Institute La Jolla, CA, USA.
Amanda J RobertsDepartment of Molecular and Cellular Neuroscience, The Scripps Research Institute La Jolla, CA, USA ; Molecular and Cellular Neuroscience Department, Mouse Behavioral Assessment Core, The Scripps Research Institute La Jolla, CA, USA.
Youssef SariDepartment of Pharmacology, College of Pharmacy and Pharmaceutical Sciences, University of Toledo Toledo, OH, USA.
Richard L BellDepartment of Psychiatry, Indiana University School of Medicine Indianapolis, IN, USA.
Eric A EnglemanDepartment of Psychiatry, Indiana University School of Medicine Indianapolis, IN, USA.
Indiana University – Purdue University Indianapolis · USScripps Research Institute · USIndiana University School of MedicineUniversity of Toledo · US

Funding

Rat Animal Models Core (RAMC)U01AA013522 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2001 to 2014
$4.3M
Scripps Genetic Animal Models Core ComponentU01AA013523 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTS, AMANDA J · 2001 to 2010
$2.7M
Rat Animal Models & Drug and Gene Testing Core (RAM-DGTC)U24AA013522 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2015 to 2021
$2.4M
Mouse Target Assessment CoreU01AA020893 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTS, AMANDA J · 2011 to 2015
$1.5M
Consequences of voluntary intake of ethanol & nicotine during peri-adolescenceR01AA020396 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI BELL, RICHARD LOWELL, ENGLEMAN, ERIC A. · 2012 to 2016
$1.2M
The role of GLT1 in the modulation of alcohol-drinking behavior in P rats.R01AA019458 · NIAAA · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI SARI, YOUSSEF · 2011 to 2015
$1.1M
NIAAA NIH HHS R01 AA019458NIAAA NIH HHS R01 AA020396NIAAA NIH HHS U01 AA013522NIAAA NIH HHS U01 AA013523NIAAA NIH HHS U01 AA020893NIAAA NIH HHS U24 AA013522
6 · The paper itself

Abstract

Alcohol and drug abuse take a large toll on society and affected individuals. However, very few effective treatments are currently available to treat alcohol and drug addiction. Basic and clinical research has begun to provide some insights into the underlying neurobiological systems involved in the addiction process. Several neurotransmitter pathways have been implicated and distinct reward neurocircuitry have been proposed-including the mesocorticolimbic dopamine (MCL-DA) system and the extended amygdala. The serotonin (5-HT) neurotransmitter system is of particular interest and multiple 5-HT receptors are thought to play significant roles in alcohol and drug self-administration and the development of drug dependence. Among the 5-HT receptors, the 5-HT7 receptor is currently undergoing characterization as a potential target for the treatment of several psychiatric disorders. Although this receptor has received only limited research regarding addictive behaviors, aspects of its neuroanatomical, biochemical, physiological, pharmacological, and behavioral profiles suggest that it could play a key role in the addiction process. For instance, genomic studies in humans have suggested a link between variants in the gene encoding the 5-HT7 receptor and alcoholism. Recent behavioral testing using high-affinity antagonists in mice and preliminary tests with alcohol-preferring rats suggest that this receptor could mediate alcohol consumption and/or reinforcement and play a role in seeking/craving behavior. Interest in the development of new and more selective pharmacological agents for this receptor will aid in examining the 5-HT7 receptor as a novel target for treating addiction.

Indexed as

alcohol abusedrug abusegeneticsmesocorticolimbic dopamine systempharmacogeneticsselective breedingserotonin-7 (5-HT7)

Identifiers

PMID25628528
PMCPMC4292232
OpenAlexW2059236014

What OpenQuestion holds

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LicenceCC BY
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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.