Treatment With Methotrexate Associated With Lipid Core Nanoparticles Prevents Aortic Dilation in a Murine Model of Marfan Syndrome.

Marfan syndrome adenosine aortic dilation inflammation lipid nanoparticle

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 10 03 2022
accepted: 13 04 2022
entrez: 27 6 2022
pubmed: 28 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

In Marfan syndrome (MFS), dilation, dissection, and rupture of the aorta occur. Inflammation can be involved in the pathogenicity of aortic defects and can thus be a therapeutic target for MFS. Previously, we showed that the formulation of methotrexate (MTX) associated with lipid nanoparticles (LDE) has potent anti-inflammatory effects without toxicity. To investigate whether LDEMTX treatment can prevent the development of aortic lesions in the MFS murine model. MgΔloxPneo MFS (

Identifiants

pubmed: 35757348
doi: 10.3389/fcvm.2022.893774
pmc: PMC9226570
doi:

Types de publication

Journal Article

Langues

eng

Pagination

893774

Informations de copyright

Copyright © 2022 Guido, Lopes, Albuquerque, Tavares, Jensen, Carvalho, Tavoni, Dias, Pereira, Laurindo and Maranhão.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Maria Carolina Guido (MC)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Natalia de Menezes Lopes (NM)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Camila Inagaki Albuquerque (CI)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Elaine Rufo Tavares (ER)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Leonardo Jensen (L)

Laboratory of Hypertension, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Priscila de Oliveira Carvalho (PO)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Thauany Martins Tavoni (TM)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Ricardo Ribeiro Dias (RR)

Department of Cardiovascular Surgery, Heart Institute (InCor), Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Lygia da Veiga Pereira (LDV)

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

Francisco Rafael Martins Laurindo (FRM)

Laboratory of Vascular Biology, Heart Institute (InCor), Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Raul Cavalcante Maranhão (RC)

Laboratory of Metabolism and Lipids, Heart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, Brazil.

Classifications MeSH