Evidence map›Paper›PMID 29301614›Full record

ReviewBiological psychiatry2018

Metabotropic Glutamate Receptors 2 and 3 as Targets for Treating Nicotine Addiction.

Alan J Cross, Robert Anthenelli, Xia Li

Abstract readReview
In one paragraph

Review in Biological psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. mGlu2 Receptors in the Basal Ganglia: A New Frontier in Addiction Therapy.Frontiers in bioscience (Landmark edition) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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  15. Review
  16. Article
  17. Article
  18. 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

3 authors at 2 institutions in 1 country.

Alan J CrossAstraZeneca Neuroscience Innovative Medicines, Cambridge, Massachusetts.
Robert AnthenelliDepartment of Psychiatry, School of Medicine, University of California San Diego, La Jolla, California.
Xia LiDepartment of Psychiatry, School of Medicine, University of California San Diego, La Jolla, California. Electronic address: x9li@ucsd.edu.
University of California, San Diego · USAstraZeneca (United States) · US

Funding

Lead optimization of Novel mGlu2 Negative Allosteric ModulatorsR01MH106865 · NIMH · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COSFORD, NICHOLAS DAVID, DER-AVAKIAN, ANDRE · 2016 to 2018
$2.5M
Early postnatal disruptions to glutamate and GABA systems and their contribution to reward deficitsR01MH108653 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BARNES, SAMUEL ALAN · 2016 to 2020
$2.0M
Neurobiology of Nicotine Reward and WithdrawalR56DA011946 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MARKOU, ATHINA · 2013 to 2014
$659k
Role of metabotropic glutamate receptor expression in nicotine dependenceR21DA040195 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LI, XIA · 2015 to 2016
$424k
NIDA NIH HHS R21 DA040195NIDA NIH HHS R56 DA011946NIMH NIH HHS R01 MH106865NIMH NIH HHS R01 MH108653
6 · The paper itself

Abstract

Tobacco smoking, driven by the addictive properties of nicotine, continues to be a worldwide health problem. Based on the well-established role of glutamatergic neurotransmission in drug addiction, novel medication development strategies seek to halt nicotine consumption and prevent relapse to tobacco smoking by modulating glutamate transmission. The presynaptic inhibitory metabotropic glutamate receptors 2 and 3 (mGluR2/3) are key autoreceptors on glutamatergic terminals that maintain glutamate homeostasis. Accumulating evidence suggests the critical role of mGluR2/3 in different aspects of nicotine addiction, including acquisition and maintenance of nicotine taking, nicotine withdrawal, and persistent nicotine seeking even after prolonged abstinence. The involvement of mGluR2/3 in other neuropsychiatric conditions, such as anxiety, depression, schizophrenia, Alzheimer's disease, Parkinson's disease, and pain, provides convincing evidence suggesting that mGluR2/3 may provide an effective therapeutic approach for comorbidity of smoking and these conditions. This focused review article highlights that mGluR2/3 provide a promising target in the search for smoking cessation medication with novel mechanisms of actions that differ from those of currently U.S. Food and Drug Administration-approved pharmacotherapies.

Indexed as

AnimalsBehavior, AddictiveBrainExcitatory Amino Acid AntagonistsHumansNicotinic AgonistsReceptors, Metabotropic GlutamateSelf AdministrationSmokingSmoking CessationTobacco Use DisorderExcitatory Amino Acid Antagonistsmetabotropic glutamate receptor 2metabotropic glutamate receptor 3Nicotinic AgonistsReceptors, Metabotropic GlutamateAddictionMetabotropic glutamate receptor 2/3MicotineRelapseRewardWithdrawal

Identifiers

PMID29301614
PMCPMC5953779
OpenAlexW2769652487

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.