Institute of Biomedical Sciences, Department of Physiology, Biochemistry, Microbiology and Laboratory Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Consultation and Diagnostic Center, Vilnius District Central Polyclinic, Vilnius, Lithuania.
Med Sci Monit Basic Res. 2021 Feb 15;27:e929634. doi: 10.12659/MSMBR.929634.
BACKGROUND Oxidative stress (OS) is known to be extremely damaging for phospholipids in cell membranes, especially their polyunsaturated fatty acids (PUFAs). OS is known to be associated with increased platelet activation and thrombosis, which lead to cardiovascular lesions. The aim of this study was to investigate how changes in the composition of fatty acids (FAs) in the platelet phospholipid membrane correlate with OS in healthy men and in men who have experienced a myocardial infarction (post-MI men). MATERIAL AND METHODS FA methyl esters from the platelet phospholipid membrane of 79 apparently healthy and 20 post-MI men were identified using gas chromatography/mass spectrometry. Malondialdehyde (MDA) was measured in the blood serum using high-performance liquid chromatography, and platelet-white blood cell aggregates (PWAs) were analysed based on whole-blood flow cytometry. The composition of platelet membrane FAs was compared to MDA concentration (µg/l) and the percentage of PWA formation between healthy men and individuals who had suffered a myocardial infarction (MI). RESULTS Statistically, post-MI patients had a significantly higher concentration of blood serum MDA than those in the control group (p=0.000). The level of PUFAs was also higher in the platelet phospholipid membrane of post-MI patients than in healthy individuals (p=0.016). However, the percentage of PWA formation was lower in patients compared with the control group (p<0.05). CONCLUSIONS A higher level of blood serum MDA concentration due to OS stimulates platelets to incorporate more PUFAs into the phospholipid membrane, thereby affecting platelet activation. This may lead the individual to develop cardiovascular diseases in the future.
氧化应激(OS)已知对细胞膜中的磷脂,尤其是多不饱和脂肪酸(PUFA)有极强的破坏作用。OS 与血小板活化和血栓形成增加有关,进而导致心血管损伤。本研究旨在探讨健康男性和心肌梗死(MI)后男性血小板磷脂膜中脂肪酸(FA)组成的变化与 OS 之间的关系。
采用气相色谱/质谱法鉴定 79 名健康男性和 20 名 MI 后男性血小板磷脂膜中的 FA 甲酯。采用高效液相色谱法测定血清中的丙二醛(MDA),并根据全血流动 cytometry 分析血小板-白细胞聚集体(PWA)。将血小板膜 FA 的组成与 MDA 浓度(µg/l)和 MI 后个体的 PWA 形成百分比进行比较。
统计分析显示,MI 后患者的血清 MDA 浓度明显高于对照组(p=0.000)。MI 后患者血小板磷脂膜中的多不饱和脂肪酸(PUFA)水平也高于健康个体(p=0.016)。然而,与对照组相比,患者的 PWA 形成百分比较低(p<0.05)。
由于 OS 导致的血清 MDA 浓度升高会刺激血小板将更多的 PUFAs 纳入磷脂膜,从而影响血小板的活化。这可能导致个体在未来患上心血管疾病。