Evidence map›Paper›PMID 37010311›Full record

ArticleJournal of visualized experiments : JoVE2023

Ferric Chloride-Induced Arterial Thrombosis and Sample Collection for 3D Electron Microscopy Analysis.

Smita Joshi, Alexis N Smith, Kanakanagavalli Shravani Prakhya, Hammodah R Alfar, Joshua Lykins, Ming Zhang, Irina Pokrovskaya, Maria Aronova, Richard D Leapman, Brian Storrie and 1 more

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

11 authors at 3 institutions in 1 country.

Smita Joshi *Department of Molecular and Cellular Biochemistry, University of Kentucky; smita.joshi@uky.edu.
Alexis N SmithDepartment of Molecular and Cellular Biochemistry, University of Kentucky.
Kanakanagavalli Shravani PrakhyaDepartment of Molecular and Cellular Biochemistry, University of Kentucky.
Hammodah R AlfarDepartment of Molecular and Cellular Biochemistry, University of Kentucky.
Joshua LykinsDepartment of Molecular and Cellular Biochemistry, University of Kentucky.
Ming ZhangDepartment of Molecular and Cellular Biochemistry, University of Kentucky.
Irina PokrovskayaDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences.
Maria AronovaLaboratory of Cellular Imaging and Macromolecular Biophysics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health.
Richard D LeapmanLaboratory of Cellular Imaging and Macromolecular Biophysics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health.
Brian StorrieDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences.
Sidney W Whiteheart *Department of Molecular and Cellular Biochemistry, University of Kentucky; whitehe@uky.edu.
University of Kentucky · USNational Institutes of Health · USUniversity of Arkansas for Medical Sciences · US

Funding

Three-Dimensional Cell and Tissue Reconstruction by Serial Block Face SEMZIAEB000086 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI LEAPMAN, RICHARD · 2013 to 2025
$23.6M
Resubmission: Structure/Function Determinants of Puncture Wound Thrombus FormationR01HL155519 · NHLBI · UNIV OF ARKANSAS FOR MED SCIS · PI STORRIE, BRIAN · 2021 to 2024
$2.5M
NHLBI NIH HHS R01 HL155519
6 · The paper itself

Abstract

Cardiovascular diseases are a leading cause of mortality and morbidity worldwide. Aberrant thrombosis is a common feature of systemic conditions like diabetes and obesity, and chronic inflammatory diseases like atherosclerosis, cancer, and autoimmune diseases. Upon vascular injury, usually the coagulation system, platelets, and endothelium act in an orchestrated manner to prevent bleeding by forming a clot at the site of the injury. Abnormalities in this process lead to either excessive bleeding or uncontrolled thrombosis/insufficient antithrombotic activity, which translates into vessel occlusion and its sequelae. The FeCl3-induced carotid injury model is a valuable tool in probing how thrombosis initiates and progresses in vivo. This model involves endothelial damage/denudation and subsequent clot formation at the injured site. It provides a highly sensitive, quantitative assay to monitor vascular damage and clot formation in response to different degrees of vascular damage. Once optimized, this standard technique can be used to study the molecular mechanisms underlying thrombosis, as well as the ultrastructural changes in platelets in a growing thrombus. This assay is also useful to study the efficacy of antithrombotic and antiplatelet agents. This article explains how to initiate and monitor FeCl3-induced arterial thrombosis and how to collect samples for analysis by electron microscopy.

Indexed as

Fibrinolytic AgentsThrombosisBlood PlateletsChloridesFerric CompoundsHemorrhageHumansMicroscopy, ElectronChloridesferric chlorideFerric CompoundsFibrinolytic Agents

Identifiers

PMID37010311
PMCPMC11042049
OpenAlexW4327709785

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.