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2
High fat feeding in mice is insufficient to induce cardiac dysfunction and does not exacerbate heart failure.给小鼠喂食高脂肪食物不足以诱发心脏功能障碍,也不会加剧心力衰竭。
PLoS One. 2013 Dec 18;8(12):e83174. doi: 10.1371/journal.pone.0083174. eCollection 2013.
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Heart disease and stroke statistics--2014 update: a report from the American Heart Association.《2014年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2014 Jan 21;129(3):e28-e292. doi: 10.1161/01.cir.0000441139.02102.80. Epub 2013 Dec 18.
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Obesity paradox in different populations: evidence and controversies.不同人群中的肥胖悖论:证据与争议
Future Cardiol. 2014 Jan;10(1):81-91. doi: 10.2217/fca.13.84.
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Obesity paradox and the heart: which indicator of obesity best describes this complex relationship?肥胖悖论与心脏:哪种肥胖指标能最好地描述这种复杂关系?
Curr Opin Clin Nutr Metab Care. 2013 Sep;16(5):517-24. doi: 10.1097/MCO.0b013e328363bcca.
6
Body mass index and stroke: overweight and obesity less often associated with stroke recurrence.体重指数与中风:超重和肥胖与中风复发的相关性较低。
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NF-κB-mediated induction of autophagy in cardiac ischemia/reperfusion injury.NF-κB 介导的自噬在心肌缺血/再灌注损伤中的诱导作用。
Biochem Biophys Res Commun. 2013 Jun 28;436(2):180-5. doi: 10.1016/j.bbrc.2013.05.070. Epub 2013 May 29.
8
The protective roles of autophagy in ischemic preconditioning.自噬在缺血预处理中的保护作用。
Acta Pharmacol Sin. 2013 May;34(5):636-43. doi: 10.1038/aps.2013.18. Epub 2013 Apr 22.
9
Role of Beclin 1-dependent autophagy in cardioprotection of ischemic preconditioning.Beclin 1依赖性自噬在缺血预处理心脏保护中的作用。
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10
Activation of autophagy in ischemic postconditioning contributes to cardioprotective effects against ischemia/reperfusion injury in rat hearts.缺血后处理中自噬的激活有助于减轻大鼠心肌缺血/再灌注损伤的心脏保护作用。
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缺血再灌注前急性摄入高脂饮食可通过NF-κB依赖的自噬途径调节实现心脏保护。

Acute consumption of a high-fat diet prior to ischemia-reperfusion results in cardioprotection through NF-κB-dependent regulation of autophagic pathways.

作者信息

Haar Lauren, Ren Xiaoping, Liu Yong, Koch Sheryl E, Goines Jillian, Tranter Michael, Engevik Melinda A, Nieman Michelle, Rubinstein Jack, Jones W Keith

机构信息

Department of Systems Biology and Physiology, University of Cincinnati, Cincinnati, Ohio;

Department of Internal Medicine, Division of Cardiovascular Health and Disease, University of Cincinnati, Cincinnati, Ohio;

出版信息

Am J Physiol Heart Circ Physiol. 2014 Dec 15;307(12):H1705-13. doi: 10.1152/ajpheart.00271.2014. Epub 2014 Sep 19.

DOI:10.1152/ajpheart.00271.2014
PMID:25239807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5504404/
Abstract

Previous studies have demonstrated improvement of cardiac function occurs with acute consumption of a high-fat diet (HFD) after myocardial infarction (MI). However, no data exist addressing the effects of acute HFD upon the extent of injury after MI. This study investigates the hypothesis that short-term HFD, prior to infarction, protects the heart against ischemia-reperfusion (I/R) injury through NF-κB-dependent regulation of cell death pathways in the heart. Data show that an acute HFD initiates cardioprotection against MI (>50% reduction in infarct size normalized to risk region) after 24 h to 2 wk of HFD, but protection is completely absent after 6 wk of HFD, when mice are reported to develop pathophysiology related to the diet. Furthermore, cardioprotection after 24 h of HFD persists after an additional 24 h of normal chow feeding and was found to be dependent upon NF-κB activation in cardiomyocytes. This study also indicates that short-term HFD activates autophagic processes (beclin-1, LC-3) preischemia, as seen in other protective stimuli. Increases in beclin-1 and LC-3 were found to be NF-κB-dependent, and administration of chloroquine, an inhibitor of autophagy, abrogated cardioprotection. Our results support that acute high-fat feeding mediates cardioprotection against I/R injury associated with a NF-κB-dependent increase in autophagy and reduced apoptosis, as has been found for ischemic preconditioning.

摘要

先前的研究表明,心肌梗死后急性摄入高脂饮食(HFD)可改善心脏功能。然而,尚无关于急性高脂饮食对心肌梗死后损伤程度影响的数据。本研究探讨了以下假设:梗死前短期高脂饮食通过心脏中细胞死亡途径的NF-κB依赖性调节来保护心脏免受缺血再灌注(I/R)损伤。数据显示,急性高脂饮食在高脂饮食24小时至2周后可启动针对心肌梗死的心脏保护作用(梗死面积相对于危险区域减少>50%),但在高脂饮食6周后完全没有保护作用,此时据报道小鼠出现了与饮食相关的病理生理学变化。此外,高脂饮食24小时后的心脏保护作用在再给予24小时正常饲料喂养后仍然存在,并且发现其依赖于心肌细胞中的NF-κB激活。本研究还表明,短期高脂饮食会在缺血前激活自噬过程(贝林1、微管相关蛋白轻链3),其他保护性刺激也可见此现象。发现贝林1和微管相关蛋白轻链3的增加是NF-κB依赖性的,自噬抑制剂氯喹的给药消除了心脏保护作用。我们的结果支持,急性高脂喂养介导了针对缺血再灌注损伤的心脏保护作用,这与缺血预处理一样,与NF-κB依赖性自噬增加和细胞凋亡减少有关。