(-)-Epicatechin Ameliorates Cardiac Fibrosis in a Female Rat Model of Pre-Heart Failure with Preserved Ejection Fraction.


Journal

Journal of medicinal food
ISSN: 1557-7600
Titre abrégé: J Med Food
Pays: United States
ID NLM: 9812512

Informations de publication

Date de publication:
Aug 2022
Historique:
pubmed: 3 8 2022
medline: 23 8 2022
entrez: 2 8 2022
Statut: ppublish

Résumé

One of the most abundant flavonoids present in cacao is (-)-epicatechin (Epi) and this flavanol has been linked to the cardiovascular health promoting actions of cocoa products. We previously demonstrated that Epi reduces infarct size in rodent models of ischemia/reperfusion and permanent coronary occlusion. Reduced infarct size was associated with decreased left ventricular (LV) oxidative stress (OS) and indicators of inflammation factors, which foster myocardial fibrosis. In this study, we examine the antifibrotic actions of Epi in an aging female rat model of pre-heart failure with preserved ejection fraction (pre-HFpEF) as well as its potential to mitigate plasma levels of OS, proinflammatory/profibrotic cytokines, and improve passive and active LV function. Epi treatment [1 mg/(kg·d)] was provided daily by gavage from 21 to 22 months of age, whereas controls received water. A Millar catheter was used to assess hemodynamic function. Subsequently, hearts were arrested in diastole, a balloon inserted into the LV and passive pressure-volume curves generated. Fixed LV sections were processed for collagen area fraction quantification using Sirius Red staining. Treatment with Epi did not lead to detectable changes in LV contractile function. However, passive LV pressure volume curves were significantly right shifted with Epi. Collagen area fraction values indicated that Epi treatment significantly reduces LV fibrosis. Epi also significantly reduced plasma OS markers and levels of profibrotic and proinflammatory cytokines. In conclusion, Epi reduces cardiac fibrosis in an aged, female rat model of pre-HFpEF, which correlates with significant reductions in OS and cytokine levels in the absence of changes in LV contractile function.

Identifiants

pubmed: 35917528
doi: 10.1089/jmf.2021.0158
pmc: PMC9419952
doi:

Substances chimiques

Cytokines 0
Catechin 8R1V1STN48
Collagen 9007-34-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

836-844

Subventions

Organisme : BLRD VA
ID : I01 BX003230
Pays : United States

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Auteurs

Moises Bustamante-Pozo (M)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.
Departamento de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.

Israel Ramirez-Sanchez (I)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.
Departamento de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.

Alejandra Garate-Carrillo (A)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.
Departamento de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.

Bruce Ito (B)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.

Viridiana Navarrete (V)

Departamento de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.

Moises Haro (M)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.

Ricardo Garcia (R)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.
Cardiovascular and Fibrotic Diseases Department, Brystol-Myers Squibb, New York, New York, USA.

Nancy Carson (N)

Cardiovascular and Fibrotic Diseases Department, Brystol-Myers Squibb, New York, New York, USA.

Guillermo Ceballos (G)

Departamento de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.

Francisco Villarreal (F)

Department of Medicine, School of Medicine, University of California, San Diego, La Jolla, California, USA.
Research Department, VA San Diego Health Care, San Diego, California, USA.

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Classifications MeSH