Literature DB >> 24657595

Functional and structural alterations of cardiac and skeletal muscle mitochondria in heart failure patients.

Gustavo Guzmán Mentesana1, Alejandra L Báez1, María S Lo Presti1, Ricardo Domínguez2, Roque Córdoba3, Carolina Bazán1, Mariana Strauss1, Ricardo Fretes4, Héctor W Rivarola1, Patricia Paglini-Oliva5.   

Abstract

BACKGROUND AND AIMS: The fundamental mechanisms involved in the genesis and progression of heart failure are not clearly understood. The present study was conducted to analyze the cardiac mitochondrial involvement in heart failure, the possible parallelism between cardiac and skeletal muscle and if there is a link between clinical symptoms and mitochondrial damage.
METHODS: Left ventricle and pectoral biopsies were obtained from patients with heart failure (n: 21) and patients with inter-auricular communication as the unique diagnosis for surgery (n: 6). Mitochondria were isolated from these tissues and studied through electron microscopy, spectrophotometry to measure the activity of respiratory complex III and immunohistochemistry to determine the presence of reactive oxygen species.
RESULTS: More than 90% of cardiac and skeletal muscle mitochondria presented structural and functional alterations in relation to an increment in the reactive oxygen species production, even in patients without the presence of any clinical Framingham criteria.
CONCLUSIONS: We demonstrated some parallelism between cardiac and skeletal muscle mitochondrial alterations in patients with heart failure and that these alterations begin before the major clinical Framingham criteria are installed, pointing to mitochondria as one of the possibly responsible factors for the evolution of cardiac disease.
Copyright © 2014 IMSS. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cardiac and skeletal muscle; Heart failure; Mitochondria

Mesh:

Substances:

Year:  2014        PMID: 24657595     DOI: 10.1016/j.arcmed.2014.03.003

Source DB:  PubMed          Journal:  Arch Med Res        ISSN: 0188-4409            Impact factor:   2.235


  6 in total

1.  Monocyte glycolysis determines CD8+ T cell functionality in human Chagas disease.

Authors:  Liliana María Sanmarco; Natalia Eberhardt; Gastón Bergero; Luz Piedad Quebrada Palacio; Pamela Martino Adami; Laura Marina Visconti; Ángel Ramón Minguez; Yolanda Hernández-Vasquez; Eugenio Antonio Carrera Silva; Laura Morelli; Miriam Postan; Maria Pilar Aoki
Journal:  JCI Insight       Date:  2019-09-19

2.  Drug Targets for Heart Failure with Preserved Ejection Fraction: A Mechanistic Approach and Review of Contemporary Clinical Trials.

Authors:  Ravi B Patel; Sanjiv J Shah
Journal:  Annu Rev Pharmacol Toxicol       Date:  2018-10-08       Impact factor: 13.820

Review 3.  Iron therapy for the treatment of iron deficiency in chronic heart failure: intravenous or oral?

Authors:  Theresa McDonagh; Iain C Macdougall
Journal:  Eur J Heart Fail       Date:  2015-01-30       Impact factor: 15.534

4.  High-fat diet affects skeletal muscle mitochondria comparable to pressure overload-induced heart failure.

Authors:  Estelle Heyne; Andrea Schrepper; Torsten Doenst; Christina Schenkl; Katrin Kreuzer; Michael Schwarzer
Journal:  J Cell Mol Med       Date:  2020-05-04       Impact factor: 5.310

5.  Mitochondrial Dysfunction Underlies Cardiomyocyte Remodeling in Experimental and Clinical Atrial Fibrillation.

Authors:  Marit Wiersma; Denise M S van Marion; Rob C I Wüst; Riekelt H Houtkooper; Deli Zhang; Natasja M S de Groot; Robert H Henning; Bianca J J M Brundel
Journal:  Cells       Date:  2019-10-05       Impact factor: 6.600

Review 6.  Impact of Mitophagy and Mitochondrial Unfolded Protein Response as New Adaptive Mechanisms Underlying Old Pathologies: Sarcopenia and Non-Alcoholic Fatty Liver Disease.

Authors:  Rodrigo Urbina-Varela; Nataly Castillo; Luis A Videla; Andrea Del Campo
Journal:  Int J Mol Sci       Date:  2020-10-18       Impact factor: 5.923

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.