Evidence map›Paper›PMID 19477168›Full record

ReviewBiochemical pharmacology2009

Alpha9 nicotinic acetylcholine receptors and the treatment of pain.

J Michael McIntosh, Nathan Absalom, Mary Chebib, Ana Belén Elgoyhen, Michelle Vincler

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

79 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
  2. GABAMedComm · 2025
    Review
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  9. Review
  10. Marine drugs · 2022
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  11. Article
  12. GABACurrent topics in behavioral neurosciences · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 3 countries.

J Michael McIntoshDepartment of Psychiatry, University of Utah, Salt Lake City, UT 84132, USA. mcintosh.mike@gmail.com
Nathan Absalom
Mary Chebib
Ana Belén Elgoyhen
Michelle Vincler
University of Sydney · AUExperimental Medicine and Biology Institute · ARUniversity of Utah · USWake Forest University · US

Funding

Venoms, Biological Resources, Molecular BiologyP01GM048677 · NIGMS · UNIVERSITY OF UTAH · PI BANDYOPADHYAY, PRADIP K · 1993 to 2018
$32.2M
Novel Neuronal nAChR-Targeted PeptidesR01MH053631 · NIMH · UNIVERSITY OF UTAH · PI MCINTOSH, J MICHAEL · 2001 to 2011
$3.6M
Nicotinic Acetylcholine Receptors in Neuropathic PainR01NS048158 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI VINCLER, MICHELLE A · 2005 to 2008
$666k
NOVEL NEURONAL NACHR-TARGETED PEPTIDESR29MH053631 · NIMH · UNIVERSITY OF UTAH · PI MCINTOSH, J MICHAEL · 1996 to 2000
$107k
NIGMS NIH HHS GM48677NIGMS NIH HHS P01 GM048677NIMH NIH HHS MH53631NIMH NIH HHS N01 MH032004NIMH NIH HHS R01 MH053631NIMH NIH HHS R29 MH053631NINDS NIH HHS NS048158NINDS NIH HHS R01 NS048158
6 · The paper itself

Abstract

Chronic pain is a vexing worldwide problem that causes substantial disability and consumes significant medical resources. Although there are numerous analgesic medications, these work through a small set of molecular mechanisms. Even when these medications are used in combination, substantial amounts of pain often remain. It is therefore highly desirable to develop treatments that work through distinct mechanisms of action. While agonists of nicotinic acetylcholine receptors (nAChRs) have been intensively studied, new data suggest a role for selective antagonists of nAChRs. alpha-Conotoxins are small peptides used offensively by carnivorous marine snails known as Conus. A subset of these peptides known as alpha-conotoxins RgIA and Vc1.1 produces both acute and long lasting analgesia. In addition, these peptides appear to accelerate the recovery of function after nerve injury, possibly through immune mediated mechanisms. Pharmacological analysis indicates that RgIA and Vc1.1 are selective antagonists of alpha9alpha10 nAChRs. A recent study also reported that these alpha9alpha10 antagonists are also potent GABA-B agonists. In the current study, we were unable to detect RgIA or Vc1.1 binding to or action on cloned GABA-B receptors expressed in HEK cells or Xenopus oocytes. We review the background, findings and implications of use of compounds that act on alpha9* nAChRs.(1).

Indexed as

AnalgesicsAnimalsConotoxinsGABA-B Receptor AgonistsHumansNicotinic AgonistsNicotinic AntagonistsPainProtein MultimerizationProtein SubunitsReceptors, GABA-BReceptors, NicotinicRecombinant ProteinsAnalgesicsCHRNA9 protein, humanChrna9 protein, mouseChrna9 protein, ratConotoxinsGABA-B Receptor AgonistsNicotinic AgonistsNicotinic AntagonistsProtein SubunitsReceptors, GABA-BReceptors, NicotinicRecombinant Proteins

Identifiers

PMID19477168
PMCPMC2739401
OpenAlexW1996065721

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.