DISCOVERIES (ISSN 2359-7232), 2021, July-September issue

CITATION: 

Liehn EA, Lupan AM, Diaconu R, Ioana M, Streata S, Manole C, Burlacu AHeart function assessment during aging in apolipoprotein E knock-out mice. Discoveries 2021, 9(3): e136. DOI: 10.15190/d.2021.15


Submitted: September 08, 2021; Revised: September 23, 2021; Accepted: September 28, 2021; Published: September 28, 2021; 

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Heart function assessment during aging in apolipoprotein E knock-out mice

Elisa A. Liehn (1,2,3,*), Ana-Mihaela Lupan (4), Rodica Diaconu (1,2), Mihai Ioana (1), Ioana Streata (1), Catalin Manole (3), Alexandrina Burlacu (4)

(1) Human Genetic Laboratory, University of Medicine and Pharmacy of Craiova, Craiova, Romania

(2) Department of Cardiology, Angiology and Intensive Care, Medical Faculty, University Hospital Aachen, Aachen, Germany

(3) Victor Babes National Institute of Pathology, Bucharest, Romania 

(4) Nicolae Simionescu Institute of Cellular Biology and Pathology, Bucharest, Romania


*Corresponding authors: Dr. Elisa A. Liehn, Department of Cardiology, Angiology and Intensive Care, Medical Faculty, University Hospital Aachen, Germany; Phone: +49-241-80 35983; Email: eliehn@ukaachen.de

Disclosure: Corresponding author, Prof. Elisa A Liehn, is a Senior Editor of the journal Discoveires. This article had 2 Editors assigned, namely Professor Bhanu P. Jena (USA) and Prof. Damodar Gupta (India).

Abstract

BACKGROUND: Apolipoprotein (apo) E isoforms have strong correlations with metabolic and cardiovascular diseases. However, it is not clear if apoE has a role in development of non-ischemic cardiomyopathy. Our study aims to analyze the involvement of apoE in non-ischemic cardiomyopathy.

METHODS AND RESULTS: Serial echo-cardiographic measurements were performed in old wildtype and apoE deficient (apoE-/-) mice. Morphological and functional cardiac parameters were in normal range in both groups at the age of 12 month. At the age of 18 months, both groups had shown ventricular dilation and increased heart rates. However, the apoE-/- mice presented signs of diastolic dysfunction by hypertrophic changes in left ventricle, due probably to arterial hypertension. The right ventricle was not affected by age or genotype. 

CONCLUSION: Even in the absence of high fat diet, apoE deficiency in mice induces mild changes in the cardiac function of the left ventricle during aging, by developing diastolic dysfunction, which leads to heart failure with preserved ejection fraction. However, further studies are necessary to conclude over the role of apoE in cardiac physiology and its involvement in development of heart failure.

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