Evidence map›Paper›PMID 23272693›Full record

ReviewDiscovery medicine2012

Emerging approaches for treatment of schizophrenia: modulation of cholinergic signaling.

Daniel J Foster, Carrie K Jones, P Jeffrey Conn

Abstract readReview
In one paragraph

Review in Discovery medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
–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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Histamine HNature communications · 2021
    Article
  8. Biomolecules · 2020
    Article
  9. Article
  10. Long-term effects of maternal choline supplementation on CA1 pyramidal neuron gene expression in the Ts65Dn mouse model of Down syndrome and Alzheimer's disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Article
  12. An Integrative and Mechanistic Model of Impaired Belief Updating in Schizophrenia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  13. Article
  14. Article
  15. Positive allosteric modulation of MNeuropharmacology · 2018
    Review
  16. Total RNA Sequencing of Rett Syndrome Autopsy Samples Identifies the MThe Journal of pharmacology and experimental therapeutics · 2018
    Article
  17. Review
  18. Article
  19. Review
  20. Drug models of schizophrenia.Therapeutic advances in psychopharmacology · 2015
    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.

Daniel J FosterDepartment of Pharmacology and Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University Medical Center, Nashville, Tennessee 37202, USA.
Carrie K Jones
P Jeffrey Conn

Funding

Vanderbilt NCDDDG for Discovery of Novel Treatments for SchizophreniaU01MH087965 · NIMH · VANDERBILT UNIVERSITY · PI CONN, P JEFFREY, LINDSLEY, CRAIG · 2010 to 2014
$9.3M
Muscarinic receptor activators as novel antipsychotic agentsR01MH073676 · NIMH · VANDERBILT UNIVERSITY · PI Jerri Michelle Rook · 2006 to 2026
$9.3M
Pharmacological modulation of striatal physiology and repetitive behaviors by M4 PAMsR01MH122545 · NIMH · VANDERBILT UNIVERSITY · PI FOSTER, DANIEL J · 2021 to 2025
$2.0M
M4 Positive Allosteric Modulators for the Treatment of SchizophreniaR01MH086601 · NIMH · VANDERBILT UNIVERSITY · PI JONES, CARRIE KIMBERLY · 2009 to 2013
$1.9M
Elucidation of M5 Muscarinic Receptor Neurophysiology using Allosteric ModulatorsF32MH095285 · NIMH · VANDERBILT UNIVERSITY · PI FOSTER, DANIEL J · 2011 to 2013
$151k
NIMH NIH HHS F32 MH095285NIMH NIH HHS R01 MH073676NIMH NIH HHS R01 MH086601NIMH NIH HHS R01 MH122545NIMH NIH HHS U01 MH087965
6 · The paper itself

Abstract

Currently available therapeutic agents for treatment of schizophrenia target signaling by monoaminergic neurotransmitters; however, these treatments do not adequately treat the range of symptoms observed in patients. While these therapies treat the positive symptoms, they do not have efficacy in treating the negative symptoms and cognitive deficits that are associated with the disease. Evidence suggests that molecules that modulate signaling by the neurotransmitter acetylcholine (ACh) could provide a more comprehensive treatment of schizophrenia than currently prescribed antipsychotics. Molecules that broadly increase ACh-signaling have been demonstrated to have efficacy in treating numerous symptom clusters in schizophrenia patients. Unfortunately, these compounds induce adverse effects via activation of peripheral receptors that limit their clinical utility. One proposed strategy for retaining the efficacy of cholinergic treatments, without the adverse effects, is to target specific cholinergic receptor subtypes in the brain. Several cholinergic receptors are able to modulate brain circuits that are dysregulated in schizophrenia patients including receptors belonging to both the muscarinic family (i.e., M1, M4, and M5), and the nicotinic family (i.e., α7, α4β2). Recently, great strides have been made in developing small molecules with high specificity for these receptors, and several of these novel molecules have robust efficacy in several preclinical models predictive of both anti-psychotic and pro-cognitive effectiveness. Promising studies suggest that targeting M1 and α7 may be beneficial for pro-cognitive effects, while molecules that target M4 may be ideally suited to address the positive symptoms. Since these receptor subtypes are distinct from those responsible for the adverse effects observed with non-selective cholinergic treatments, there is hope that molecules targeting these receptors could provide novel therapeutics. Further research is needed to examine the utility of such compounds as therapeutics that could be used either alone, or in combination with existing medications, to better treat schizophrenia.

Indexed as

Signal TransductionAllosteric RegulationAnimalsCholinergic NeuronsHumansReceptors, MuscarinicReceptors, NicotinicSchizophreniaReceptors, MuscarinicReceptors, Nicotinic

Identifiers

PMID23272693
PMCPMC3726271

What OpenQuestion holds

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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.