Bioactive lipids improve serum HDL and PON1 activities in coronary artery disease patients: Ex-vivo study

IF 3.5 3区 医学 Q2 PHARMACOLOGY & PHARMACY Vascular pharmacology Pub Date : 2024-10-15 DOI:10.1016/j.vph.2024.107435
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Abstract

Background

Atherosclerotic cardiovascular disease (CVD) remains a leading cause of vascular disease worldwide. Atherosclerosis is characterized by the accumulation of lipids and oxidized lipids on the blood vessel walls. Coronary artery disease (CAD) is the most common display of atherosclerotic CVD.

Objectives

We investigated the effects of the bioactive lipids as lyso-diacylglyceryltrimethylhomoserine (lyso-DGTS (20,5,0)) and its derivative oleoyl-N-trimethyl homoserine amide (oleoyl amide-MHS) on the properties and functionality of HDL and paraoxonase 1 (PON1) activities in the serum of individuals who exhibited arterial plaque as observed by coronary CT angiography (CCTA).

Methods

The study included two independent groups comprising 40 patients who had undergone arterial CCTA scans at Ziv Medical Center for various medical indications. The CAD group included 20 patients with coronary artery plaques with luminal stenosis of more than 50 % in a major coronary vessel. The control group consisted of 20 healthy patients (patients without artery plaques).

Results

Serum samples from CAD patients exhibited lower serum PON1 and cholesterol efflux activities and higher pro-inflammatory than the control group. HDL isolated from CAD patients contains elevated levels of oxidizing lipids (specifically lyso- phosphatidyl ethanolamines and lyso-phosphocholines(compared to the control. However, incubation of the CAD patients' serum with lyso-DGTS and oleoyl amide-MHS restored the antiatherogenic activities of HDL. The lipids increased serum PON1 activities, enhanced apoB-depleted serum cholesterol-efflux activity, and elevated the serum's anti-inflammatory properties.

Conclusions

The results of the present study suggest the potential of the bioactive lipids lyso-DGTS and oleoyl amide-MHS to attenuate atherosclerosis via the improvement of dysfunctional HDL properties and PON1 activities. Further, in-vivo experiments are needed to assess the athero-protective effect of the lipids.

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生物活性脂质可改善冠心病患者的血清高密度脂蛋白和 PON1 活性:体外研究
背景:动脉粥样硬化性心血管疾病(CVD)仍然是全球血管疾病的主要病因。动脉粥样硬化的特点是脂质和氧化脂质在血管壁上堆积。冠状动脉疾病(CAD)是动脉粥样硬化性心血管疾病最常见的表现形式:我们研究了溶血二酰甘油三甲基高丝氨酸(lyso-DGTS (20,5,0))及其衍生物油酰基-N-三甲基高丝氨酸酰胺(油酰基酰胺-MHS)等生物活性脂质对冠状动脉 CT 血管造影(CCTA)观察到的动脉斑块患者血清中高密度脂蛋白的性质和功能以及副氧合酶 1(PON1)活性的影响:该研究包括两个独立的小组,由 40 名因各种医疗指征在 Ziv 医疗中心接受动脉 CCTA 扫描的患者组成。CAD 组包括 20 名冠状动脉斑块患者,其主要冠状动脉管腔狭窄超过 50%。对照组包括 20 名健康患者(无动脉斑块):结果:与对照组相比,CAD 患者的血清样本显示出较低的血清 PON1 和胆固醇外排活性以及较高的促炎性。与对照组相比,从 CAD 患者体内分离出的 HDL 含有更高水平的氧化脂质(特别是溶血磷脂酰乙醇胺和溶血磷脂酰胆碱)。然而,用溶菌酶-DGTS 和油酰基酰胺-MHS 培养 CAD 患者的血清,可恢复 HDL 的抗动脉粥样硬化活性。这些脂质提高了血清中 PON1 的活性,增强了载脂蛋白耗竭的血清胆固醇外流活性,并提高了血清的抗炎特性:本研究的结果表明,生物活性脂质溶菌-DGTS 和油酰基酰胺-MHS 有可能通过改善功能失调的高密度脂蛋白特性和 PON1 活性来减轻动脉粥样硬化。此外,还需要进行体内实验来评估这些脂质的动脉粥样硬化保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vascular pharmacology
Vascular pharmacology 医学-药学
CiteScore
6.60
自引率
2.50%
发文量
153
审稿时长
31 days
期刊介绍: Vascular Pharmacology publishes papers, which contains results of all aspects of biology and pharmacology of the vascular system. Papers are encouraged in basic, translational and clinical aspects of Vascular Biology and Pharmacology, utilizing approaches ranging from molecular biology to integrative physiology. All papers are in English. The Journal publishes review articles which include vascular aspects of thrombosis, inflammation, cell signalling, atherosclerosis, and lipid metabolism.
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