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Western diet increases cardiac ceramide content in healthy and hypertrophied hearts
T J Butler1, D Ashford2, A-M Seymour1
1School of Biological, Biomedical and Environmental Sciences, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK.
Insights
A Western-style diet (WD) exacerbates cardiac remodeling in obesity and left ventricular hypertrophy (LVH). This diet increases harmful ceramide species, raising susceptibility to heart failure (HF).
Area of Science:
- Cardiovascular Science
- Metabolic Research
- Cellular Biology
Background:
- Obesity and left ventricular hypertrophy (LVH) are independent risk factors for heart failure (HF).
- The combined impact of obesity and LVH on cardiovascular disease progression requires further elucidation.
- Cellular metabolic alterations in LVH may lead to lipotoxicity and apoptosis.
Purpose of the Study:
- To investigate the effects of dietary changes on cardiac metabolism in obese hearts with LVH.
- To understand the mechanisms linking diet, obesity, LVH, and cardiovascular disease.
Main Methods:
- Cardiac hypertrophy was induced by aortic constriction (AC) in an animal model.
- Animals were fed standard, high-fat, or Western-style diets for 9 weeks.
- Cardiac metabolism, lipid content, and ceramide species were analyzed.
Main Results:
- The Western-style diet (WD) accelerated weight gain and worsened LVH.
- WD significantly reduced cardiac fatty acid oxidation and increased triacylglycerol.
- Cardiac ceramide content increased in WD groups, with exacerbated remodeling in a heart failure model.
Conclusions:
- Diet-induced obesity and LVH lead to inappropriate cardiac ceramide accumulation, increasing cell death risk.
- Combined high fat and sugar intake promotes pathological cardiac remodeling.
- This dietary pattern is linked to adverse cardiovascular outcomes.
Background And Aims:
Obesity and cardiac left ventricular hypertrophy (LVH) are recognised independent risk factors in the development of heart failure (HF). However, the combination of these factors may exacerbate the onset of cardiovascular disease by mechanisms as yet unclear. LVH leads to significant cellular remodelling, including alterations in metabolism which may result in an inappropriate accumulation of lipids and eventual lipotoxicity and apoptosis. The aim of the study was to determine the impact of dietary manipulation on cardiac metabolism in the obese and hypertrophied heart.
Methods And Results:
LVH was induced via aortic constriction (AC) in an experimental model of cardiac hypertrophy and animals subjected to 9 weeks of dietary manipulation with either a standard, high fat, or a sucrose containing Western-style diet (SD, HFD and WD, respectively). This latter diet resulted in accelerated weight gain in both LVH/AC and control animals. LVH was greater in AC animals fed a WD, and both control and AC animals from this diet showed a significant reduction in cardiac fatty acid oxidation and increased triacylglycerol content. Ceramide content was significantly increased in the WD groups, with no additional effect of LVH. Comparison with a model of HF induced by exposure to Doxorubicin and WD showed exacerbated remodelling of cardiac ceramide species leading to increased C16 and C18 content.
Conclusions:
These findings highlight the inappropriate accumulation and re-distribution of cardiac ceramide species in a diet-induced model of obesity and LVH, potentially increasing susceptibility to cell death. The combination of increased fat and sugar leads to greater pathological remodelling and may explain why this diet pattern is consistently linked with poor cardiovascular outcomes.
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