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Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology

OBJECTIVE: Heart failure with preserved ejection fraction (HFpEF) is a public health problem worldwide. Treatments for the patients with HFpEF are not satisfactory because there is no unified understanding of the pathological mechanism of HFpEF. This study aims at investigating the potential patholo...

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Autores principales: Xu, Hang, Gao, Kai, Liu, Chao, Li, Tian, Ding, Yi, Ma, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163871/
https://www.ncbi.nlm.nih.gov/pubmed/37159835
http://dx.doi.org/10.7717/peerj.15280
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author Xu, Hang
Gao, Kai
Liu, Chao
Li, Tian
Ding, Yi
Ma, Jing
author_facet Xu, Hang
Gao, Kai
Liu, Chao
Li, Tian
Ding, Yi
Ma, Jing
author_sort Xu, Hang
collection PubMed
description OBJECTIVE: Heart failure with preserved ejection fraction (HFpEF) is a public health problem worldwide. Treatments for the patients with HFpEF are not satisfactory because there is no unified understanding of the pathological mechanism of HFpEF. This study aims at investigating the potential pathological mechanism for the effective diagnosis and treatment of HFpEF. METHODS: Ten adult male Dahl salt sensitive rats (180–200 g) were divided into control and model groups. The rats in model group were fed with high salt diet (8% NaCl) to induce HFpEF for this comparative study. Behavioral changes, biochemical parameters, and histopathological changes of the rats were detected. iTRAQ technology combined with bioinformatics analysis was employed to study the differentially expressed proteins (DEPs) and their enrichment in signaling pathways. RESULTS: Echocardiography detection showed decreased LVEF, indicating impaired cardiac function (P < 0.01), increased LVPWd, indicating ventricular wall hypertrophy (P < 0.05), prolonged duration of IVRT and decreased E/A ratio, indicating diastolic dysfunction (P < 0.05) of the rats in model group. 563 DEPs were identified in the rats of both groups, with 243 up-regulated and 320 down-regulated. The expression of PPAR signaling pathway in the rats of model group was down-regulated, with PPARα most significantly decreased (91.2%) (P < 0.01), PPARγ obviously decreased (63.60%) (P < 0.05), and PPARβ/δ decreased (45.33%) (P < 0.05). The DEPs enriched in PPAR signaling pathway were mainly related to such biological processes as fatty acid beta-oxidation, such cellular components as peroxisome, and such molecular functions as lipid binding. CONCLUSIONS: NaCl high salt diet is one of the factors to increase the incidence of HFpEF in rats. PPARα, PPARγ and PPAR β/δ might be the targets of HFpEF. The findings may provide a theoretical basis for the treatment of HFpEF in clinical practice.
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spelling pubmed-101638712023-05-07 Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology Xu, Hang Gao, Kai Liu, Chao Li, Tian Ding, Yi Ma, Jing PeerJ Biochemistry OBJECTIVE: Heart failure with preserved ejection fraction (HFpEF) is a public health problem worldwide. Treatments for the patients with HFpEF are not satisfactory because there is no unified understanding of the pathological mechanism of HFpEF. This study aims at investigating the potential pathological mechanism for the effective diagnosis and treatment of HFpEF. METHODS: Ten adult male Dahl salt sensitive rats (180–200 g) were divided into control and model groups. The rats in model group were fed with high salt diet (8% NaCl) to induce HFpEF for this comparative study. Behavioral changes, biochemical parameters, and histopathological changes of the rats were detected. iTRAQ technology combined with bioinformatics analysis was employed to study the differentially expressed proteins (DEPs) and their enrichment in signaling pathways. RESULTS: Echocardiography detection showed decreased LVEF, indicating impaired cardiac function (P < 0.01), increased LVPWd, indicating ventricular wall hypertrophy (P < 0.05), prolonged duration of IVRT and decreased E/A ratio, indicating diastolic dysfunction (P < 0.05) of the rats in model group. 563 DEPs were identified in the rats of both groups, with 243 up-regulated and 320 down-regulated. The expression of PPAR signaling pathway in the rats of model group was down-regulated, with PPARα most significantly decreased (91.2%) (P < 0.01), PPARγ obviously decreased (63.60%) (P < 0.05), and PPARβ/δ decreased (45.33%) (P < 0.05). The DEPs enriched in PPAR signaling pathway were mainly related to such biological processes as fatty acid beta-oxidation, such cellular components as peroxisome, and such molecular functions as lipid binding. CONCLUSIONS: NaCl high salt diet is one of the factors to increase the incidence of HFpEF in rats. PPARα, PPARγ and PPAR β/δ might be the targets of HFpEF. The findings may provide a theoretical basis for the treatment of HFpEF in clinical practice. PeerJ Inc. 2023-05-03 /pmc/articles/PMC10163871/ /pubmed/37159835 http://dx.doi.org/10.7717/peerj.15280 Text en ©2023 Xu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Xu, Hang
Gao, Kai
Liu, Chao
Li, Tian
Ding, Yi
Ma, Jing
Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title_full Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title_fullStr Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title_full_unstemmed Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title_short Pathological mechanism of heart failure with preserved ejection fraction in rats based on iTRAQ technology
title_sort pathological mechanism of heart failure with preserved ejection fraction in rats based on itraq technology
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163871/
https://www.ncbi.nlm.nih.gov/pubmed/37159835
http://dx.doi.org/10.7717/peerj.15280
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