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在代偿性心肌肥大腹主动脉缩窄模型中对心脏代谢和功能的体内评估。

In vivo assessment of cardiac metabolism and function in the abdominal aortic banding model of compensated cardiac hypertrophy.

作者信息

Seymour Anne-Marie L, Giles Lucia, Ball Vicky, Miller Jack J, Clarke Kieran, Carr Carolyn A, Tyler Damian J

机构信息

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

Department of Physiology, Anatomy and Genetics, University of Oxford, Sherrington Building, Parks Road, Oxford OX1 3PT, UK.

出版信息

Cardiovasc Res. 2015 May 1;106(2):249-60. doi: 10.1093/cvr/cvv101. Epub 2015 Mar 5.

Abstract

AIMS

Left ventricular hypertrophy is an adaptive response of the heart to chronic mechanical overload and can lead to functional deterioration and heart failure. Changes in cardiac energy metabolism are considered as key to the hypertrophic remodelling process. The concurrence of obesity and hypertrophy has been associated with contractile dysfunction, and this work therefore aimed to investigate the in vivo structural, functional, and metabolic remodelling that occurs in the hypertrophied heart in the setting of a high-fat, high-sucrose, Western diet (WD).

METHODS AND RESULTS

Following induction of cardiac hypertrophy through abdominal aortic banding, male Sprague Dawley rats were exposed to either a standard diet or a WD (containing 45% fat and 16% sucrose) for up to 14 weeks. Cardiac structural and functional characteristics were determined by CINE MRI, and in vivo metabolism was investigated using hyperpolarized (13)C-labelled pyruvate. Cardiac hypertrophy was observed at all time points, irrespective of dietary manipulation, with no evidence of cardiac dysfunction. Pyruvate dehydrogenase flux was unchanged in the hypertrophied animals at any time point, but increased incorporation of the (13)C label into lactate was observed by 9 weeks and maintained at 14 weeks, indicative of enhanced glycolysis.

CONCLUSION

Hypertrophied hearts revealed little evidence of a switch towards increased glucose oxidation but rather an uncoupling of glycolytic metabolism from glucose oxidation. This was maintained under conditions of dietary stress provided by a WD but, at this compensated phase of hypertrophy, did not result in any contractile dysfunction.

摘要

目的

左心室肥厚是心脏对慢性机械性负荷的适应性反应,可导致功能恶化和心力衰竭。心脏能量代谢的变化被认为是肥厚性重塑过程的关键。肥胖与肥厚同时存在与收缩功能障碍有关,因此本研究旨在探讨在高脂、高糖的西式饮食(WD)环境下,肥厚心脏中发生的体内结构、功能和代谢重塑。

方法与结果

通过腹主动脉缩窄诱导心脏肥厚后,将雄性Sprague Dawley大鼠暴露于标准饮食或WD(含45%脂肪和16%蔗糖)中长达14周。通过电影磁共振成像(CINE MRI)测定心脏结构和功能特征,并使用超极化(13)C标记的丙酮酸研究体内代谢。在所有时间点均观察到心脏肥厚,与饮食干预无关,且无心脏功能障碍的证据。在任何时间点,肥厚动物的丙酮酸脱氢酶通量均未改变,但在9周时观察到(13)C标记物掺入乳酸的增加,并在14周时维持,表明糖酵解增强。

结论

肥厚心脏几乎没有证据表明向增加葡萄糖氧化转变,而是糖酵解代谢与葡萄糖氧化解偶联。在WD提供的饮食应激条件下,这种情况得以维持,但在肥厚的这个代偿阶段,并未导致任何收缩功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f8/4400188/6449b4e59472/cvv10101.jpg

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