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西方饮食会增加健康心脏和肥厚心脏中的心脏神经酰胺含量。

Western diet increases cardiac ceramide content in healthy and hypertrophied hearts.

作者信息

Butler T J, Ashford D, Seymour A-M

机构信息

School of Biological, Biomedical and Environmental Sciences, Hull York Medical School, University of Hull, Hull, HU6 7RX, UK.

Technology Facility (Proteomics & Analytical Biochemistry Laboratory), Centre of Excellence in Mass Spectrometry, Department of Biology, University of York, UK.

出版信息

Nutr Metab Cardiovasc Dis. 2017 Nov;27(11):991-998. doi: 10.1016/j.numecd.2017.08.007. Epub 2017 Sep 7.

Abstract

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.

摘要

背景与目的

肥胖和心脏左心室肥厚(LVH)是公认的心力衰竭(HF)发生发展的独立危险因素。然而,这些因素的联合作用可能通过尚不清楚的机制加剧心血管疾病的发生。LVH导致显著的细胞重塑,包括代谢改变,这可能导致脂质的不适当积累以及最终的脂毒性和细胞凋亡。本研究的目的是确定饮食干预对肥胖和肥厚心脏心脏代谢的影响。

方法与结果

在心脏肥大的实验模型中,通过主动脉缩窄(AC)诱导LVH,并对动物进行为期9周的饮食干预,分别采用标准饮食、高脂饮食或含蔗糖的西式饮食(分别为SD、HFD和WD)。后一种饮食导致LVH/AC组和对照组动物体重加速增加。喂食WD的AC动物LVH更严重,且该饮食组的对照组和AC动物均显示心脏脂肪酸氧化显著降低,三酰甘油含量增加。WD组神经酰胺含量显著增加,LVH无额外影响。与阿霉素和WD诱导的HF模型相比,心脏神经酰胺种类的重塑加剧,导致C16和C18含量增加。

结论

这些发现突出了在饮食诱导的肥胖和LVH模型中心脏神经酰胺种类的不适当积累和重新分布,可能增加细胞死亡的易感性。脂肪和糖增加的联合作用导致更大程度的病理重塑,这可能解释了为什么这种饮食模式一直与不良心血管结局相关。

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