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Rivaroxaban improves vascular response in LPS-induced acute inflammation in experimental models.
Daci, Armond; Da Dalt, Lorenzo; Alaj, Rame; Shurdhiqi, Shpejtim; Neziri, Burim; Ferizi, Rrahman; Danilo Norata, Giuseppe; Krasniqi, Shaip.
Afiliación
  • Daci A; Department of Pharmacy, Faculty of Medicine, University of Prishtina, Prishtina, Kosovo.
  • Da Dalt L; Institute of Pharmacology and Toxicology, Faculty of Medicine, University of Prishtina, Prishtina, Kosovo.
  • Alaj R; Department of Excellence of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.
  • Shurdhiqi S; Cardiovascular Surgery Clinic, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Neziri B; Cardiovascular Surgery Clinic, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Ferizi R; Institute of Pathophysiology, Faculty of Medicine, University of Prishtina, Prishtina, Kosovo.
  • Danilo Norata G; Department of Premedical Courses-Biology, Faculty of Medicine, University of Prishtina, Prishtina, Kosovo.
  • Krasniqi S; Department of Excellence of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.
PLoS One ; 15(12): e0240669, 2020.
Article en En | MEDLINE | ID: mdl-33301454
Rivaroxaban (RVX) was suggested to possess anti-inflammatory and vascular tone modulatory effects. The goal of this study was to investigate whether RVX impacts lipopolysaccharide (LPS)-induced acute vascular inflammatory response. Male rats were treated with 5 mg/kg RVX (oral gavage) followed by 10 mg/kg LPS i.p injection. Circulating levels of IL-6, MCP-1, VCAM-1, and ICAM-1 were measured in plasma 6 and 24 hours after LPS injection, while isolated aorta was used for gene expression analysis, immunohistochemistry, and vascular tone evaluation. RVX pre-treatment significantly reduced LPS mediated increase after 6h and 24h for IL-6 (4.4±2.2 and 2.8±1.7 fold), MCP-1 (1.4±1.5 and 1.3±1.4 fold) VCAM-1 (1.8±2.0 and 1.7±2.1 fold). A similar trend was observed in the aorta for iNOS (5.5±3.3 and 3.3±1.9 folds reduction, P<0.01 and P<0.001, respectively), VCAM-1 (1.3±1.2 and 1.4±1.3 fold reduction, P<0.05), and MCP-1 (3.9±2.2 and 1.9±1.6 fold reduction, P<0.01). Moreover, RVX pre-treatment, improved LPS-induced PE contractile dysfunction in aortic rings (Control vs LPS, Emax reduction = 35.4 and 31.19%, P<0.001; Control vs LPS+RVX, Emax reduction = 10.83 and 11.48%, P>0.05, respectively), resulting in 24.5% and 19.7% change in maximal constriction in LPS and LPS+RVX respectively. These data indicate that RVX pre-treatment attenuates LPS-induced acute vascular inflammation and contractile dysfunction.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vasculitis / Vasoconstricción / Rivaroxabán / Antiinflamatorios Límite: Animals / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vasculitis / Vasoconstricción / Rivaroxabán / Antiinflamatorios Límite: Animals / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos