Evidence map›Paper›PMID 35867038›Full record

ArticleJournal of visualized experiments : JoVE2022

DetectSyn: A Rapid, Unbiased Fluorescent Method to Detect Changes in Synapse Density.

Chelcie F Heaney, Colin J McArdle, Kimberly F Raab-Graham

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 92% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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.

Chelcie F HeaneyWake Forest Translational Alcohol Research Center, Wake Forest School of Medicine; Physiology and Pharmacology, Wake Forest School of Medicine.
Colin J McArdlePhysiology and Pharmacology, Wake Forest School of Medicine.
Kimberly F Raab-GrahamWake Forest Translational Alcohol Research Center, Wake Forest School of Medicine; Physiology and Pharmacology, Wake Forest School of Medicine; kraabgra@wakehealth.edu.
Wake Forest University · US

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Colleen A Hanlon · 2018 to 2026
$16.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
Mechanisms of Alcohol WithdrawalR01AA016852 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI GODWIN, DWAYNE W · 2008 to 2024
$5.5M
Molecular Mechanism of Hippocampal network excitability in a novel, in vivo model of Tuberous Sclerosis ComplexR01NS105005 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RAAB-GRAHAM, KIMBERLY FRANCES · 2018 to 2022
$1.9M
Biochemical Studies Underlying Acute Ethanol's Antidepressant-like effects during Withdrawal in a Preclinical Model of Ethanol DependenceR01AA029691 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Kimberly Frances Raab-Graham · 2023 to 2026
$1.4M
NIAAA NIH HHS P50 AA026117NIAAA NIH HHS R01 AA016852NIAAA NIH HHS R01 AA029691NIAAA NIH HHS T32 AA007565NINDS NIH HHS R01 NS105005
6 · The paper itself

Abstract

Synapses are the site of communication between neurons. Neuronal circuit strength is related to synaptic density, and the breakdown of synapses is characteristic of disease states like major depressive disorder (MDD) and Alzheimer's disease. Traditional techniques to investigate synapse numbers include genetic expression of fluorescent markers (e.g., green fluorescent protein (GFP)), dyes that fill a neuron (e.g., carbocyanine dye, DiI), and immunofluorescent detection of spine markers (e.g., postsynaptic density 95 (PSD95)). A major caveat to these proxy techniques is that they only identify postsynaptic changes. Yet, a synapse is a connection between a presynaptic terminal and a postsynaptic spine. The gold standard for measuring synapse formation/elimination requires time-consuming electron microscopy or array tomography techniques. These techniques require specialized training and costly equipment. Further, only a limited number of neurons can be assessed and are used to represent changes to an entire brain region. DetectSyn is a rapid fluorescent technique that identifies changes to synapse formation or elimination due to a disease state or drug activity. DetectSyn utilizes a rapid proximity ligation assay to detect juxtaposed pre- and postsynaptic proteins and standard fluorescent microscopy, a technique readily available to most laboratories. Fluorescent detection of the resulting puncta allows for quick and unbiased analysis of experiments. DetectSyn provides more representative results than electron microscopy because larger areas can be analyzed than a limited number of fluorescent neurons. Moreover, DetectSyn works for in vitro cultured neurons and fixed tissue slices. Finally, a method is provided to analyze the data collected from this technique. Overall, DetectSyn offers a procedure for detecting relative changes in synapse density across treatments or disease states and is more accessible than traditional techniques.

Indexed as

Major Depressive DisorderCells, CulturedColoring AgentsHippocampusHumansNeuronsPresynaptic TerminalsSynapsesColoring Agents

Identifiers

PMID35867038
PMCPMC13360286
OpenAlexW4286624379

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.