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心恶液质与心力衰竭的关联——心脏肥胖的保护作用。

Interconnection between Cardiac Cachexia and Heart Failure-Protective Role of Cardiac Obesity.

机构信息

Department of Immunology, Instituto Nacional de Cardiología "Ignacio Chávez", México City 14080, Mexico.

Department of Cardiovascular Biomedicine, Instituto Nacional de Cardiología "Ignacio Chávez", México City 14080, Mexico.

出版信息

Cells. 2022 Mar 18;11(6):1039. doi: 10.3390/cells11061039.

Abstract

Cachexia may be caused by congestive heart failure, and it is then called cardiac cachexia, which leads to increased morbidity and mortality. Cardiac cachexia also worsens skeletal muscle degradation. Cardiac cachexia is the loss of edema-free muscle mass with or without affecting fat tissue. It is mainly caused by a loss of balance between protein synthesis and degradation, or it may result from intestinal malabsorption. The loss of balance in protein synthesis and degradation may be the consequence of altered endocrine mediators such as insulin, insulin-like growth factor 1, leptin, ghrelin, melanocortin, growth hormone and neuropeptide Y. In contrast to many other health problems, fat accumulation in the heart is protective in this condition. Fat in the heart can be divided into epicardial, myocardial and cardiac steatosis. In this review, we describe and discuss these topics, pointing out the interconnection between heart failure and cardiac cachexia and the protective role of cardiac obesity. We also set the basis for possible screening methods that may allow for a timely diagnosis of cardiac cachexia, since there is still no cure for this condition. Several therapeutic procedures are discussed including exercise, nutritional proposals, myostatin antibodies, ghrelin, anabolic steroids, anti-inflammatory substances, beta-adrenergic agonists, medroxyprogesterone acetate, megestrol acetate, cannabinoids, statins, thalidomide, proteasome inhibitors and pentoxifylline. However, to this date, there is no cure for cachexia.

摘要

恶病质可能由充血性心力衰竭引起,此时称为心脏恶病质,会导致发病率和死亡率增加。心脏恶病质还会加剧骨骼肌降解。心脏恶病质是指无水肿肌肉质量的丢失,无论是否影响脂肪组织。它主要是由于蛋白质合成和降解之间失去平衡引起的,也可能是由于肠道吸收不良所致。蛋白质合成和降解之间的平衡失调可能是胰岛素、胰岛素样生长因子 1、瘦素、胃饥饿素、黑素细胞刺激素、生长激素和神经肽 Y 等内分泌介质改变的结果。与许多其他健康问题不同,这种情况下心脏脂肪堆积具有保护作用。心脏中的脂肪可分为心外膜脂肪、心肌脂肪和心脏脂肪变性。在这篇综述中,我们描述并讨论了这些主题,指出了心力衰竭和心脏恶病质之间的相互关系以及心脏肥胖的保护作用。我们还为可能的筛查方法奠定了基础,以便及时诊断心脏恶病质,因为目前对此病尚无治愈方法。我们还讨论了几种治疗方法,包括运动、营养建议、肌肉生长抑制素抗体、胃饥饿素、合成代谢类固醇、抗炎物质、β-肾上腺素能激动剂、醋酸甲羟孕酮、醋酸甲地孕酮、大麻素、他汀类药物、他昔莫芬、蛋白酶体抑制剂和己酮可可碱。然而,迄今为止,恶病质仍无法治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a69/8946995/15040119b40a/cells-11-01039-g001.jpg

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