Evidence map›Paper›PMID 38797778›Full record

ArticleScientific reports2024

Effect of hypercholesterolemia on circulating and cardiomyocyte-derived extracellular vesicles.

Csenger Kovácsházi, Szabolcs Hambalkó, Nabil V Sayour, Tamás G Gergely, Gábor B Brenner, Csilla Pelyhe, Dóra Kapui, Bennet Y Weber, Alexander L Hültenschmidt, Éva Pállinger and 13 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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
–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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Reduced circulating CD63Cardiovascular diabetology · 2024
    Article
  5. Article
  6. 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

23 authors.

Csenger Kovácsházi *Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Szabolcs Hambalkó *Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Nabil V SayourDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Tamás G GergelyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Gábor B BrennerDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Csilla PelyheDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Dóra KapuiDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Bennet Y WeberDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Alexander L HültenschmidtDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Éva PállingerInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Edit I BuzásInstitute of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Ádám ZolcsákDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Bálint KissDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Tamás BozóDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Csilla CsányiDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Nikolett KósaDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Miklós KellermayerDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Róbert FarkasDepartment of Laboratory Medicine, Laboratory of Mass Spectrometry and Separation Technology, Semmelweis University, Budapest, Hungary.
Gellért B KarvalyDepartment of Laboratory Medicine, Laboratory of Mass Spectrometry and Separation Technology, Semmelweis University, Budapest, Hungary.
Kieran WynneSystems Biology Ireland and School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
David MatallanasSystems Biology Ireland and School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Péter FerdinandyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Zoltán GiriczDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary. giricz.zoltan@semmelweis.hu.

Funding

Magyarország Kormánya EFOP-3.6.3-VEKOP-16-2017-00009Nemzeti Kutatási és Technológiai Hivatal K139105Science Foundation Ireland 18/RI/5702
6 · The paper itself

Abstract

Hypercholesterolemia (HC) induces, propagates and exacerbates cardiovascular diseases via various mechanisms that are yet not properly understood. Extracellular vesicles (EVs) are involved in the pathomechanism of these diseases. To understand how circulating or cardiac-derived EVs could affect myocardial functions, we analyzed the metabolomic profile of circulating EVs, and we performed an in-depth analysis of cardiomyocyte (CM)-derived EVs in HC. Circulating EVs were isolated with Vezics technology from male Wistar rats fed with high-cholesterol or control chow. AC16 human CMs were treated with Remembrane HC supplement and EVs were isolated from cell culture supernatant. The biophysical properties and the protein composition of CM EVs were analyzed. THP1-ASC-GFP cells were treated with CM EVs, and monocyte activation was measured. HC diet reduced the amount of certain phosphatidylcholines in circulating EVs, independently of their plasma level. HC treatment significantly increased EV secretion of CMs and greatly modified CM EV proteome, enriching several proteins involved in tissue remodeling. Regardless of the treatment, CM EVs did not induce the activation of THP1 monocytes. In conclusion, HC strongly affects the metabolome of circulating EVs and dysregulates CM EVs, which might contribute to HC-induced cardiac derangements.

Indexed as

Extracellular VesiclesHypercholesterolemiaMyocytes, CardiacRats, WistarAnimalsHumansMaleMonocytesRatsDyslipidemiaExosomeInflammationMetabolomicsObesityProteomics

Identifiers

PMID38797778
PMCPMC11128454

What Socratic 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 Socratic graph.