Peterson Stephen J, Choudhary Abu, Kalsi Amardeep K, Zhao Shuyang, Alex Ragin, Abraham Nader G
Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
Department of Medicine, New York Presbyterian Brooklyn Methodist Hospital, Brooklyn, NY 11215, USA.
Diagnostics (Basel). 2020 Nov 20;10(11):976. doi: 10.3390/diagnostics10110976.
In this review, we will evaluate how high-density lipoprotein (HDL) and the reverse cholesterol transport (RCT) pathway are critical for proper cardiovascular-renal physiology. We will begin by reviewing the basic concepts of HDL cholesterol synthesis and pathway regulation, followed by cardiorenal syndrome (CRS) pathophysiology. After explaining how the HDL and RCT pathways become dysfunctional through oxidative processes, we will elaborate on the potential role of HDL dysfunction in CRS. We will then present findings on how HDL function and the inducible antioxidant gene heme oxygenase-1 (HO-1) are interconnected and how induction of HO-1 is protective against HDL dysfunction and important for the proper functioning of the cardiovascular-renal system. This will substantiate the proposal of HO-1 as a novel therapeutic target to prevent HDL dysfunction and, consequently, cardiovascular disease, renal dysfunction, and the onset of CRS.
在本综述中,我们将评估高密度脂蛋白(HDL)和逆向胆固醇转运(RCT)途径对心血管 - 肾脏正常生理功能的关键作用。我们将首先回顾HDL胆固醇合成和途径调节的基本概念,随后阐述心肾综合征(CRS)的病理生理学。在解释HDL和RCT途径如何通过氧化过程发生功能障碍后,我们将详细说明HDL功能障碍在CRS中的潜在作用。然后,我们将展示关于HDL功能与诱导型抗氧化基因血红素加氧酶 - 1(HO - 1)如何相互关联,以及HO - 1的诱导对HDL功能障碍具有保护作用且对心血管 - 肾脏系统的正常运作至关重要的研究结果。这将证实HO - 1作为预防HDL功能障碍以及由此导致的心血管疾病、肾功能障碍和CRS发作的新型治疗靶点的提议。