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鞘脂类的黑暗面:寻找潜在的心血管生物标志物。

The Dark Side of Sphingolipids: Searching for Potential Cardiovascular Biomarkers.

机构信息

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi, Italy.

Vascular Physiopathology Unit, IRCCS Neuromed, 86077 Pozzilli, Italy.

出版信息

Biomolecules. 2023 Jan 13;13(1):168. doi: 10.3390/biom13010168.

DOI:10.3390/biom13010168
PMID:36671552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9855992/
Abstract

Cardiovascular diseases (CVDs) are the leading cause of death and illness in Europe and worldwide, responsible for a staggering 47% of deaths in Europe. Over the past few years, there has been increasing evidence pointing to bioactive sphingolipids as drivers of CVDs. Among them, most studies place emphasis on the cardiovascular effect of ceramides and sphingosine-1-phosphate (S1P), reporting correlation between their aberrant expression and CVD risk factors. In experimental in vivo models, pharmacological inhibition of de novo ceramide synthesis averts the development of diabetes, atherosclerosis, hypertension and heart failure. In humans, levels of circulating sphingolipids have been suggested as prognostic indicators for a broad spectrum of diseases. This article provides a comprehensive review of sphingolipids' contribution to cardiovascular, cerebrovascular and metabolic diseases, focusing on the latest experimental and clinical findings. Cumulatively, these studies indicate that monitoring sphingolipid level alterations could allow for better assessment of cardiovascular disease progression and/or severity, and also suggest them as a potential target for future therapeutic intervention. Some approaches may include the down-regulation of specific sphingolipid species levels in the circulation, by inhibiting critical enzymes that catalyze ceramide metabolism, such as ceramidases, sphingomyelinases and sphingosine kinases. Therefore, manipulation of the sphingolipid pathway may be a promising strategy for the treatment of cardio- and cerebrovascular diseases.

摘要

心血管疾病 (CVDs) 是欧洲和全球范围内导致死亡和患病的主要原因,在欧洲造成了惊人的 47%的死亡率。在过去的几年中,越来越多的证据表明生物活性神经鞘脂类物质是 CVDs 的驱动因素。其中,大多数研究都强调神经酰胺和鞘氨醇-1-磷酸 (S1P) 的心血管作用,报告了它们异常表达与 CVD 危险因素之间的相关性。在实验性体内模型中,神经酰胺从头合成的药理学抑制可预防糖尿病、动脉粥样硬化、高血压和心力衰竭的发生。在人类中,循环神经鞘脂水平被认为是多种疾病的预后指标。本文全面综述了神经鞘脂类物质对心血管、脑血管和代谢性疾病的贡献,重点介绍了最新的实验和临床发现。总之,这些研究表明,监测神经鞘脂水平的变化可以更好地评估心血管疾病的进展和/或严重程度,并表明它们可能是未来治疗干预的潜在靶点。一些方法可能包括通过抑制催化神经酰胺代谢的关键酶,如神经酰胺酶、鞘磷脂酶和鞘氨醇激酶,来下调循环中特定神经鞘脂种类的水平。因此,神经鞘脂途径的操纵可能是治疗心血管和脑血管疾病的一种有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/578a/9855992/8a890035f6d1/biomolecules-13-00168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/578a/9855992/8a890035f6d1/biomolecules-13-00168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/578a/9855992/8a890035f6d1/biomolecules-13-00168-g001.jpg

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The Acid Sphingomyelinase Inhibitor Amitriptyline Ameliorates TNF-α-Induced Endothelial Dysfunction.酸性鞘磷脂酶抑制剂阿米替林改善 TNF-α 诱导的内皮功能障碍。
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