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肺动脉高压中的代谢功能障碍

Metabolic Dysfunction in Pulmonary Arterial Hypertension.

作者信息

Assad Tufik R, Hemnes Anna R

机构信息

Division of Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, T1218 Medical Center North, 1161 21st Avenue South, Nashville, TN, 37232, USA.

出版信息

Curr Hypertens Rep. 2015 Mar;17(3):20. doi: 10.1007/s11906-014-0524-y.

Abstract

Previously considered a disease isolated to the pulmonary circulation, pulmonary arterial hypertension is now being recognized as a systemic disorder that is associated with significant metabolic dysfunction. Numerous animal models have demonstrated the development of pulmonary arterial hypertension following the onset of insulin resistance, indicating that insulin resistance may be causal. Recent publications highlighting alterations in aerobic glycolysis, fatty acid oxidation, and the tricarboxylic acid cycle in the pulmonary circulation and right ventricle have expanded our understanding of the complex pathobiology of this disease. By targeting these derangements in metabolism, numerous researchers are investigating noninvasive techniques to monitor disease activity and therapeutics that address the underlying metabolic condition. In the following review, we will explore pre-clinical and clinical studies investigating the metabolic dysfunction seen in pulmonary arterial hypertension.

摘要

肺动脉高压曾被认为是一种仅累及肺循环的疾病,现在人们认识到它是一种与显著代谢功能障碍相关的全身性疾病。众多动物模型已证明胰岛素抵抗发作后会出现肺动脉高压,这表明胰岛素抵抗可能是病因。最近的出版物强调了肺循环和右心室中需氧糖酵解、脂肪酸氧化及三羧酸循环的改变,这拓展了我们对该疾病复杂病理生物学的理解。通过针对这些代谢紊乱,众多研究人员正在研究监测疾病活动的非侵入性技术以及针对潜在代谢状况的治疗方法。在以下综述中,我们将探讨研究肺动脉高压中所见代谢功能障碍的临床前和临床研究。

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