Evidence map›Paper›PMID 35643882›Full record

ReviewCellular and molecular neurobiology2023

ACh Transfers: Homeostatic Plasticity of Cholinergic Synapses.

Sarra Djemil, Antonia M Sames, Daniel T S Pak

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Simultaneous in vivo imaging of CaThe journal of physiological sciences : JPS · 2026
    Article
  2. Review
  3. Article
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  5. Review
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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

3 authors at 1 institution in 1 country.

Sarra DjemilDepartment of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC, USA.ORCID http://orcid.org/0000-0001-8622-650X
Antonia M SamesDepartment of Biology, Georgetown University, Washington, DC, USA.ORCID http://orcid.org/0000-0003-3402-7693
Daniel T S PakDepartment of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC, USA. daniel.pak@georgetown.edu.ORCID http://orcid.org/0000-0001-5930-2589
Georgetown University · US

Funding

Translational Biomedical Science Training GrantTL1TR001431 · NCATS · GEORGETOWN UNIVERSITY · PI LEE, DEXTER L, SANDBERG, KATHRYN L · 2015 to 2024
$4.8M
Plasticity and vulnerability of basal forebrain cholinergic neurons in Alzheimer's DiseaseR21AG066016 · NIA · GEORGETOWN UNIVERSITY · PI PAK, DANIEL T · 2020 to 2020
$429k
NCATS NIH HHS TL1 TR001431NCATS NIH HHS TL1TR001431NIA NIH HHS R21 AG066016NIH HHS R21AG066016
6 · The paper itself

Abstract

The field of homeostatic plasticity continues to advance rapidly, highlighting the importance of stabilizing neuronal activity within functional limits in the context of numerous fundamental processes such as development, learning, and memory. Most homeostatic plasticity studies have been focused on glutamatergic synapses, while the rules that govern homeostatic regulation of other synapse types are less understood. While cholinergic synapses have emerged as a critical component in the etiology of mammalian neurodegenerative disease mechanisms, relatively few studies have been conducted on the homeostatic plasticity of such synapses, particularly in the mammalian nervous system. An exploration of homeostatic mechanisms at the cholinergic synapse may illuminate potential therapeutic targets for disease management and treatment. We will review cholinergic homeostatic plasticity in the mammalian neuromuscular junction, the autonomic nervous system, central synapses, and in relation to pathological conditions including Alzheimer disease and DYT1 dystonia. This work provides a historical context for the field of cholinergic homeostatic regulation by examining common themes, unique features, and outstanding questions associated with these distinct cholinergic synapse types and aims to inform future research in the field.

Indexed as

Neurodegenerative DiseasesAnimalsCholinergic AgentsHumansMammalsNeuromuscular JunctionNeuronal PlasticitySynapsesCholinergic AgentsAcetylcholineBasal forebrain cholinergic neuronsCholinergicCholinergic synapseHomeostatic plasticitySeptalSeptal-hippocampal

Identifiers

PMID35643882
PMCPMC11415198
OpenAlexW4281749772

What OpenQuestion holds

Textmetadata
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.