Evidence map›Paper›PMID 38872467›Full record

ArticlePhysiological reports2024

Innovative assessment of lipid-induced oxidative stress and inflammation in harvested human endothelial cells.

Mohammad Saleem, Taseer Ahmad, Alexandria Porcia Haynes, Claude F Albritton, Naome Mwesigwa, Meghan K Graber, Annet Kirabo, Cyndya A Shibao

Abstract read
In one paragraph

Article in Physiological reports, 2024. 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
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. 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

8 authors.

Mohammad SaleemDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Taseer AhmadDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Alexandria Porcia HaynesDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Claude F AlbrittonDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Naome MwesigwaDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Meghan K GraberDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Annet KiraboDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Cyndya A ShibaoDepartment of Medicine, Division of Clinical Pharmacology, Room 536 Robinson Research Building, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-4518-6801

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Mechanism of Glucose-dependent insulinotropic polypeptide (GIP) on Splanchnic Venous Capacitance in Postural Tachycardia SyndromeR01HL159203 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Cyndya Adriana Shibao · 2022 to 2026
$4.1M
Enhancing parasympathetic activity to reduce vascular oxidative stress and endothelial dysfunctionR01HL157584 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIRABO, ANNET, SHIBAO, CYNDYA ADRIANA · 2021 to 2024
$3.0M
Immune Mechanisms of Salt-Sensitive hypertensionR01HL144941 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIRABO, ANNET · 2021 to 2025
$3.0M
Deep phenotypic and functional characterization of salt-responsive immune cells in human salt senstive hypertension using CTE-seqR03HL155041 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIRABO, ANNET · 2021 to 2022
$173k
American heart Association 23CDA1053072American Heart Association (AHA) 967054HHS | NIH | National Center for Advancing Translational Sciences (NCATS) 5UL1TR002243-03HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL157584HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL 159203HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL144941HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R03HL155041NCATS NIH HHS UL1 TR002243NHLBI NIH HHS R01 HL144941NHLBI NIH HHS R01 HL157584NHLBI NIH HHS R01 HL159203NHLBI NIH HHS R03 HL155041
6 · The paper itself

Abstract

Studying acute changes in vascular endothelial cells in humans is challenging. We studied ten African American women and used the J-wire technique to isolate vein endothelial cells before and after a four-hour lipid and heparin infusion. Dynamic changes in lipid-induced oxidative stress and inflammatory markers were measured with fluorescence-activated cell sorting. We used the surface markers CD31 and CD144 to identify human endothelial cells. Peripheral blood mononuclear cells isolated from blood were used as a negative control. The participants received galantamine (16 mg/day) for 3 months. We previously demonstrated that galantamine treatment effectively suppresses lipid-induced oxidative stress and inflammation. In this study, we infused lipids to evaluate its potential to increase the activation of endothelial cells, as assessed by the levels of CD54+ endothelial cells and expression of Growth arrest-specific 6 compared to the baseline sample. Further, we aimed to investigate whether lipid infusion led to increased expression of the oxidative stress markers IsoLGs and nitrotyrosine in endothelial cells. This approach will expedite the in vivo identification of novel pathways linked with endothelial cell dysfunction induced by oxidative stress and inflammatory cytokines. This study describes an innovative method to harvest and study human endothelial cells and demonstrates the dynamic changes in oxidative stress and inflammatory markers release induced by lipid infusion.

Indexed as

Endothelial CellsInflammationOxidative StressAdultAntigens, CDCadherin 5CadherinsFemaleGalantamineHumansIntercellular Adhesion Molecule-1LipidsMiddle AgedPlatelet Endothelial Cell Adhesion Molecule-1Tyrosine3-nitrotyrosineAntigens, CDCadherin 5CadherinsGalantamineIntercellular Adhesion Molecule-1LipidsPECAM1 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1Tyrosineflow cytometryinflammationJ‐wire technique; endothelial cellslipidoxidative stress

Identifiers

PMID38872467
PMCPMC11176576

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.