Rivaroxaban protects from the oxysterol-induced damage and inflammatory activation of the vascular endothelium.

25-hydroxycholesterol Rivaroxaban barrier function inflammatory markers vascular endothelial damage

Journal

Tissue barriers
ISSN: 2168-8370
Titre abrégé: Tissue Barriers
Pays: United States
ID NLM: 101601065

Informations de publication

Date de publication:
02 Oct 2021
Historique:
pubmed: 30 7 2021
medline: 25 3 2022
entrez: 29 7 2021
Statut: ppublish

Résumé

Rivaroxaban is one of the direct factor Xa inhibitors. Its function in the inactivated coagulation cascade is unclear. The aim of the study was to assess the effect of rivaroxaban on the endothelial integrity and inflammatory properties of endothelial cells stimulated by 25-hydroxycholesterol (25-OHC). HUVECs were stimulated with 25-OHC, rivaroxaban and 25-OHC+ rivaroxaban. HUVEC integrity and permeability were measured using the xCELLigence system and paracellular flux assay. The mRNA expression of tissue factor, ICAM-1, VEGF, IL-33, MCP-1, TNF-α was analyzed in the real-time PCR. Apoptosis and viability were measured by flow cytometry. The VEGF protein concentration was assessed by ELISA. The confocal microscope was used to evaluate the expression of VE-cadherin in endothelial cells. 25-OHC decreased endothelial cell integrity and increased the mRNA expression of IL-33, tissue factor, ICAM-1, MCP-1, VEGF, TNF-α as compared to unstimulated controls. Following the stimulation with rivaroxaban, HUVEC restored integrity disrupted by 25-OHC ( Our finding suggests that rivaroxaban may restore the endothelial barrier and inhibit the inflammatory activation caused by oxysterol

Sections du résumé

BACKGROUND BACKGROUND
Rivaroxaban is one of the direct factor Xa inhibitors. Its function in the inactivated coagulation cascade is unclear. The aim of the study was to assess the effect of rivaroxaban on the endothelial integrity and inflammatory properties of endothelial cells stimulated by 25-hydroxycholesterol (25-OHC).
METHODS METHODS
HUVECs were stimulated with 25-OHC, rivaroxaban and 25-OHC+ rivaroxaban. HUVEC integrity and permeability were measured using the xCELLigence system and paracellular flux assay. The mRNA expression of tissue factor, ICAM-1, VEGF, IL-33, MCP-1, TNF-α was analyzed in the real-time PCR. Apoptosis and viability were measured by flow cytometry. The VEGF protein concentration was assessed by ELISA. The confocal microscope was used to evaluate the expression of VE-cadherin in endothelial cells.
RESULTS RESULTS
25-OHC decreased endothelial cell integrity and increased the mRNA expression of IL-33, tissue factor, ICAM-1, MCP-1, VEGF, TNF-α as compared to unstimulated controls. Following the stimulation with rivaroxaban, HUVEC restored integrity disrupted by 25-OHC (
CONCLUSION CONCLUSIONS
Our finding suggests that rivaroxaban may restore the endothelial barrier and inhibit the inflammatory activation caused by oxysterol

Identifiants

pubmed: 34323663
doi: 10.1080/21688370.2021.1956284
pmc: PMC8794498
doi:

Substances chimiques

Oxysterols 0
Rivaroxaban 9NDF7JZ4M3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1956284

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Auteurs

Paulina Gorzelak-Pabis (P)

Dept. of Internal Diseases and Clinical Pharmacology, The Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.

Marlena Broncel (M)

Dept. of Internal Diseases and Clinical Pharmacology, The Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.

Katarzyna Wojdan (K)

Dept. of Internal Diseases and Clinical Pharmacology, The Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.

Adrian Gajewski (A)

Department of Immunology and Allergy, Medical University of Lodz, Lodz, Poland.

Maciej Chalubinski (M)

Department of Immunology and Allergy, Medical University of Lodz, Lodz, Poland.

Mateusz Gawrysiak (M)

Department of Immunology and Allergy, Medical University of Lodz, Lodz, Poland.

Ewelina Wozniak (E)

Dept. of Internal Diseases and Clinical Pharmacology, The Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.

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Classifications MeSH