Endothelial cell-specific mineralocorticoid receptor activation promotes diastolic dysfunction in diet-induced obese male mice
Widespread consumption of diets high in fat and fructose (Western diet, WD) has led to increased prevalence of obesity and diastolic dysfunction (DD). DD is a prominent feature of heart failure with preserved ejection fraction (HFpEF). However, the underlying mechanisms of DD are poorly understood, and treatment options are still limited. We have previously shown that deletion of the cell-specific mineralocorticoid receptor in endothelial cells (ECMR) abrogates DD induced by WD feeding in female mice. However, the specific role of ECMR activation in the pathogenesis of DD in male mice has not been clarified. Therefore, we fed 4-wk-old ECMR knockout (ECMRKO) male mice and littermates (LM) with either a WD or chow diet (CD) for 16 wk. WD feeding resulted in DD characterized by increased left ventricle (LV) filling pressure (E/e') and diastolic stiffness [E/e'/LV inner diameter at end diastole (LVIDd)]. Compared with CD, WD in LM resulted in increased myocardial macrophage infiltration, oxidative stress, and increased myocardial phosphorylation of Akt, in concert with decreased phospholamban phosphorylation. WD also resulted in focal cardiomyocyte remodeling, characterized by areas of sarcomeric disorganization, loss of mitochondrial electron density, and mitochondrial fragmentation. Conversely, WD-induced DD and associated biochemical and structural abnormalities were prevented by ECMR deletion. In contrast with our previously reported observations in females, WD-fed male mice exhibited enhanced Akt signaling and a lower magnitude of cardiac injury. Collectively, our data support a critical role for ECMR in obesity-induced DD and suggest critical mechanistic differences in the genesis of DD between males and females.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:324 |
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| Enthalten in: |
American journal of physiology. Regulatory, integrative and comparative physiology - 324(2023), 1 vom: 01. Jan., Seite R90-R101 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Aroor, Annayya [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Completed 30.12.2022 Date Revised 02.01.2024 published: Print-Electronic figshare: 10.6084/m9.figshare.21561684 Citation Status MEDLINE |
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| doi: |
10.1152/ajpregu.00274.2021 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM34953795X |
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| 100 | 1 | |a Aroor, Annayya |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Endothelial cell-specific mineralocorticoid receptor activation promotes diastolic dysfunction in diet-induced obese male mice |
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| 500 | |a published: Print-Electronic | ||
| 500 | |a figshare: 10.6084/m9.figshare.21561684 | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Widespread consumption of diets high in fat and fructose (Western diet, WD) has led to increased prevalence of obesity and diastolic dysfunction (DD). DD is a prominent feature of heart failure with preserved ejection fraction (HFpEF). However, the underlying mechanisms of DD are poorly understood, and treatment options are still limited. We have previously shown that deletion of the cell-specific mineralocorticoid receptor in endothelial cells (ECMR) abrogates DD induced by WD feeding in female mice. However, the specific role of ECMR activation in the pathogenesis of DD in male mice has not been clarified. Therefore, we fed 4-wk-old ECMR knockout (ECMRKO) male mice and littermates (LM) with either a WD or chow diet (CD) for 16 wk. WD feeding resulted in DD characterized by increased left ventricle (LV) filling pressure (E/e') and diastolic stiffness [E/e'/LV inner diameter at end diastole (LVIDd)]. Compared with CD, WD in LM resulted in increased myocardial macrophage infiltration, oxidative stress, and increased myocardial phosphorylation of Akt, in concert with decreased phospholamban phosphorylation. WD also resulted in focal cardiomyocyte remodeling, characterized by areas of sarcomeric disorganization, loss of mitochondrial electron density, and mitochondrial fragmentation. Conversely, WD-induced DD and associated biochemical and structural abnormalities were prevented by ECMR deletion. In contrast with our previously reported observations in females, WD-fed male mice exhibited enhanced Akt signaling and a lower magnitude of cardiac injury. Collectively, our data support a critical role for ECMR in obesity-induced DD and suggest critical mechanistic differences in the genesis of DD between males and females | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a Research Support, N.I.H., Extramural | |
| 650 | 4 | |a Research Support, U.S. Gov't, Non-P.H.S. | |
| 650 | 4 | |a diastolic dysfunction | |
| 650 | 4 | |a endothelium | |
| 650 | 4 | |a mineralocorticoid receptor | |
| 650 | 4 | |a mitochondria | |
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| 650 | 7 | |a Receptors, Mineralocorticoid |2 NLM | |
| 650 | 7 | |a Proto-Oncogene Proteins c-akt |2 NLM | |
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| 700 | 1 | |a DeMarco, Vincent G |e verfasserin |4 aut | |
| 700 | 1 | |a Whaley-Connell, Adam T |e verfasserin |4 aut | |
| 700 | 1 | |a Jia, Guanghong |e verfasserin |4 aut | |
| 700 | 1 | |a Yang, Yan |e verfasserin |4 aut | |
| 700 | 1 | |a Sharma, Neekun |e verfasserin |4 aut | |
| 700 | 1 | |a Naz, Huma |e verfasserin |4 aut | |
| 700 | 1 | |a Hans, Chetan |e verfasserin |4 aut | |
| 700 | 1 | |a Hayden, Melvin R |e verfasserin |4 aut | |
| 700 | 1 | |a Hill, Michael A |e verfasserin |4 aut | |
| 700 | 1 | |a Sowers, James R |e verfasserin |4 aut | |
| 700 | 1 | |a Manrique-Acevedo, Camila |e verfasserin |4 aut | |
| 700 | 1 | |a Lastra, Guido |e verfasserin |4 aut | |
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