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本文引用的文献

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Endothelial Sirtuin 3 Dictates Glucose Transport to Cardiomyocyte and Sensitizes Pressure Overload-Induced Heart Failure.内皮细胞 Sirtuin 3 决定葡萄糖向心肌细胞的转运,并使压力超负荷诱导的心力衰竭敏感化。
J Am Heart Assoc. 2020 Jun 2;9(11):e015895. doi: 10.1161/JAHA.120.015895. Epub 2020 May 29.
2
Phosphodiesterase 9a Inhibition in Mouse Models of Diastolic Dysfunction.磷酸二酯酶 9a 抑制在舒张功能障碍小鼠模型中的作用。
Circ Heart Fail. 2020 May;13(5):e006609. doi: 10.1161/CIRCHEARTFAILURE.119.006609. Epub 2020 May 18.
3
Catecholamines Induce Trained Immunity in Monocytes In Vitro and In Vivo.儿茶酚胺在体外和体内诱导单核细胞产生训练有素的免疫。
Circ Res. 2020 Jul 3;127(2):269-283. doi: 10.1161/CIRCRESAHA.119.315800. Epub 2020 Apr 3.
4
Epigenetic Metabolic Reprogramming of Right Ventricular Fibroblasts in Pulmonary Arterial Hypertension: A Pyruvate Dehydrogenase Kinase-Dependent Shift in Mitochondrial Metabolism Promotes Right Ventricular Fibrosis.肺动脉高压右心室成纤维细胞的表观遗传代谢重编程:依赖于丙酮酸脱氢酶激酶的线粒体代谢转变促进右心室纤维化。
Circ Res. 2020 Jun 5;126(12):1723-1745. doi: 10.1161/CIRCRESAHA.120.316443. Epub 2020 Mar 27.
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Obesity, Hypertension, and Cardiac Dysfunction: Novel Roles of Immunometabolism in Macrophage Activation and Inflammation.肥胖、高血压和心功能障碍:免疫代谢在巨噬细胞激活和炎症中的新作用。
Circ Res. 2020 Mar 13;126(6):789-806. doi: 10.1161/CIRCRESAHA.119.312321. Epub 2020 Mar 12.
6
Monocytes present age-related changes in phospholipid concentration and decreased energy metabolism.单核细胞呈现出与年龄相关的磷脂浓度变化以及能量代谢降低。
Aging Cell. 2020 Apr;19(4):e13127. doi: 10.1111/acel.13127. Epub 2020 Feb 27.
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Aminooxyacetic acid attenuates post-infarct cardiac dysfunction by balancing macrophage polarization through modulating macrophage metabolism in mice.氨基氧乙酸通过调节巨噬细胞代谢平衡极化状态减轻小鼠心肌梗死后心功能障碍。
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免疫代谢和非心肌细胞代谢在心脏重构和损伤中的新作用。

Novel roles of immunometabolism and nonmyocyte metabolism in cardiac remodeling and injury.

机构信息

Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.

Mississippi Center for Obesity Research, University of Mississippi Medical Center, Jackson, Mississippi.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2020 Oct 1;319(4):R476-R484. doi: 10.1152/ajpregu.00188.2020. Epub 2020 Sep 2.

DOI:10.1152/ajpregu.00188.2020
PMID:32877243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7717123/
Abstract

Changes in cardiomyocyte metabolism have been heavily implicated in cardiac injury and heart failure (HF). However, there is emerging evidence that metabolism in nonmyocyte populations, including cardiac fibroblasts, immune cells, and endothelial cells, plays an important role in cardiac remodeling and adaptation to injury. Here, we discuss recent advances and insights into nonmyocyte metabolism in the healthy and injured heart. Metabolic switching from mitochondrial oxidative phosphorylation to glycolysis is critical for immune cell (macrophage and T lymphocyte) and fibroblast phenotypic switching in the inflamed and fibrotic heart. On the other hand, cardiac endothelial cells are heavily reliant on glycolytic metabolism, and thus impairments in glycolytic metabolism underlie endothelial cell dysfunction. Finally, we review current and ongoing metabolic therapies for HF and the potential implications for nonmyocyte metabolism.

摘要

心肌细胞代谢的变化与心脏损伤和心力衰竭(HF)密切相关。然而,越来越多的证据表明,非心肌细胞群(包括心脏成纤维细胞、免疫细胞和内皮细胞)的代谢在心脏重构和对损伤的适应中发挥着重要作用。在这里,我们讨论了健康和受损心脏中非心肌细胞代谢的最新进展和见解。代谢从线粒体氧化磷酸化向糖酵解的转变对于炎症和纤维化心脏中的免疫细胞(巨噬细胞和 T 淋巴细胞)和成纤维细胞表型的转变至关重要。另一方面,心脏内皮细胞严重依赖糖酵解代谢,因此糖酵解代谢受损是内皮细胞功能障碍的基础。最后,我们综述了 HF 的当前和正在进行的代谢治疗方法及其对非心肌细胞代谢的潜在影响。