Evidence map›Paper›PMID 39346680›Full record

ArticleFrontiers in molecular neuroscience2024

SR9883 is a novel small-molecule enhancer of α4β2* nicotinic acetylcholine receptor signaling that decreases intravenous nicotine self-administration in rats.

Kevin M Braunscheidel, George Voren, Christie D Fowler, Qun Lu, Alexander Kuryatov, Michael D Cameron, Ines Ibañez-Tallon, Jon M Lindstrom, Theodore M Kamenecka, Paul J Kenny

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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

10 authors.

Kevin M Braunscheidel *Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
George Voren *Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Christie D FowlerDepartment of Neurobiology and Behavior, University of California, Irvine, Irvine, CA, United States.
Qun LuThe Herbert Wertheim UF Scripps Institute for Biomedical Innovation and Technology, Jupiter, FL, United States.
Alexander KuryatovDepartment of Neuroscience, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
Michael D CameronThe Herbert Wertheim UF Scripps Institute for Biomedical Innovation and Technology, Jupiter, FL, United States.
Ines Ibañez-TallonThe Laboratory of Molecular Biology, The Rockefeller University, New York, NY, United States.
Jon M LindstromDepartment of Neuroscience, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
Theodore M KameneckaThe Herbert Wertheim UF Scripps Institute for Biomedical Innovation and Technology, Jupiter, FL, United States.
Paul J KennyNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Funding

Transcription Factors in Stimulant and Opioid ActionP01DA047233 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI YASMIN L. HURD · 2019 to 2026
$16.5M
NIDA NIH HHS P01 DA047233
6 · The paper itself

Abstract

Background: Most smokers attempting to quit will quickly relapse to tobacco use even when treated with the most efficacious smoking cessation agents currently available. This highlights the need to develop effective new smoking cessation medications. Evidence suggests that positive allosteric modulators (PAM) and other enhancers of nicotinic acetylcholine receptor (nAChR) signaling could have therapeutic utility as smoking cessation agents. Methods: 3-[3-(3-pyridyl)-1,2,4-oxadiazol-5-yl]benzonitrile (NS9283) was used as a starting point for medical chemistry efforts to develop novel small molecule enhancers of α4β2* nAChR stoichiometries containing a low-affinity agonist binding site at the interface of α4/α4 and α4/α5 subunits. Results: The NS9283 derivative SR9883 enhanced the effect of nicotine on α4β2* nAChR stoichiometries containing low-affinity agonist binding sites, with EC Conclusions: These data suggest that SR9883 is useful for investigating behavioral processes regulated by certain α4β2* nAChR stoichiometries. SR9883 and related compounds with favorable drug-like physiochemical and pharmacological properties hold promise as novel treatments of tobacco use disorder.

Indexed as

intracranial self-stimulation (ICSS)intravenous self-administration (IVSA)nicotine addictionnicotinic acetylcholine receptorsNS9283smoking cessationSR9883α4β2* nAChRs

Identifiers

PMID39346680
PMCPMC11428108

What Socratic holds

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Registered trials

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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 Socratic graph.