Literature DB >> 35917528

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

Moises Bustamante-Pozo1,2, Israel Ramirez-Sanchez1,2, Alejandra Garate-Carrillo1,2, Bruce Ito1, Viridiana Navarrete2, Moises Haro1, Ricardo Garcia1,3, Nancy Carson3, Guillermo Ceballos2, Francisco Villarreal1,4.   

Abstract

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.

Entities:  

Keywords:  HFpEF; epicatechin; fibrosis; heart failure

Mesh:

Substances:

Year:  2022        PMID: 35917528      PMCID: PMC9419952          DOI: 10.1089/jmf.2021.0158

Source DB:  PubMed          Journal:  J Med Food        ISSN: 1096-620X            Impact factor:   2.542


  29 in total

1.  Aging and Cardiac Fibrosis.

Authors:  Anna Biernacka; Nikolaos G Frangogiannis
Journal:  Aging Dis       Date:  2011-04       Impact factor: 6.745

2.  Lisinopril-mediated regression of myocardial fibrosis in patients with hypertensive heart disease.

Authors:  C G Brilla; R C Funck; H Rupp
Journal:  Circulation       Date:  2000-09-19       Impact factor: 29.690

3.  Effects of (-)-epicatechin on myocardial infarct size and left ventricular remodeling after permanent coronary occlusion.

Authors:  Katrina Go Yamazaki; Pam R Taub; Maraliz Barraza-Hidalgo; Maria M Rivas; Alexander C Zambon; Guillermo Ceballos; Francisco J Villarreal
Journal:  J Am Coll Cardiol       Date:  2010-06-22       Impact factor: 24.094

Review 4.  Flavonoids: a review of probable mechanisms of action and potential applications.

Authors:  R J Nijveldt; E van Nood; D E van Hoorn; P G Boelens; K van Norren; P A van Leeuwen
Journal:  Am J Clin Nutr       Date:  2001-10       Impact factor: 7.045

Review 5.  Flavonoids as anti-inflammatory agents.

Authors:  Mauro Serafini; Ilaria Peluso; Anna Raguzzini
Journal:  Proc Nutr Soc       Date:  2010-06-23       Impact factor: 6.297

Review 6.  Molecular mechanisms of aging-associated inflammation.

Authors:  Devanand Sarkar; Paul B Fisher
Journal:  Cancer Lett       Date:  2005-06-22       Impact factor: 8.679

7.  Advanced hypertensive heart disease in spontaneously hypertensive rats. Lisinopril-mediated regression of myocardial fibrosis.

Authors:  C G Brilla; L Matsubara; K T Weber
Journal:  Hypertension       Date:  1996-08       Impact factor: 10.190

Review 8.  Induction of cardiac fibrosis by transforming growth factor-beta(1).

Authors:  P J Lijnen; V V Petrov; R H Fagard
Journal:  Mol Genet Metab       Date:  2000 Sep-Oct       Impact factor: 4.797

9.  Chronic losartan administration reduces mortality and preserves cardiac but not skeletal muscle function in dystrophic mice.

Authors:  Lawrence T Bish; Mark Yarchoan; Meg M Sleeper; Jeffrey A Gazzara; Kevin J Morine; Pedro Acosta; Elisabeth R Barton; H Lee Sweeney
Journal:  PLoS One       Date:  2011-06-22       Impact factor: 3.240

10.  Arginase inhibition by (-)-Epicatechin reverses endothelial cell aging.

Authors:  Alejandra Garate-Carrillo; Viridiana Navarrete-Yañez; Pilar Ortiz-Vilchis; Gustavo Guevara; Carmen Castillo; Patricia Mendoza-Lorenzo; Guillermo Ceballos; Miguel Ortiz-Flores; Nayelli Najera; Moises Muratt Bustamante-Pozo; Ivan Rubio-Gayosso; Francisco Villarreal; Israel Ramirez-Sanchez
Journal:  Eur J Pharmacol       Date:  2020-08-11       Impact factor: 4.432

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