Kotur-Stevuljevic Jelena, Bogavac-Stanojevic Natasa, Jelic-Ivanovic Zorana, Stefanovic Aleksandra, Gojkovic Tamara, Joksic Jelena, Sopic Miron, Gulan Brankica, Janac Jelena, Milosevic Sanja
Institute of Medical Biochemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Special Hospital for Prevention and Therapy of Cerebrovascular Disease "Sveti Sava", Nemanjina 2, 11000 Belgrade, Serbia.
Atherosclerosis. 2015 Jul;241(1):192-8. doi: 10.1016/j.atherosclerosis.2015.05.016. Epub 2015 May 20.
The connection of oxidative stress with dyslipidemia creates a newly-emerging atherosclerosis risk factor involved in acute ischemic stroke development. This study analyzed the influence of oxidative stress on structural changes of high-density lipoprotein (HDL) particles connected with modification in protective paraoxonase 1 (PON1) activity.
This study used 185 patients with acute ischemic stroke and 185 apparently healthy controls. Oxidative stress status, PON1 status, lipids and high-sensitivity C-reactive protein (hsCRP) were determined. In isolated HDL lipoprotein fraction we determined selected markers of oxidative stress (malondialdehyde, MDA) and the content of total sulfhydryl (SH) groups. The capability of oxidative and PON1 status parameters to discriminate patients according to survival status was evaluated.
Stroke patients had lower HDL-cholesterol than controls and a remarkable fall in PON1 activity (control group-227U/L, survivors-42U/L, lethal outcome group-61U/L, p < 0.001), along with more prominent inflammation. Pronounced oxidative stress and impaired antioxidative protection was present among patients. HDL fraction analysis revealed a significant decrease of SH groups content (control group vs. patients, p < 0.05) and increased in MDA content in patients (lethal outcome vs. control group, p < 0.05). According to logistic regression analysis, the best predictor of disease outcome was oxidative stress marker - prooxidative-antioxidative balance (PAB).
Pronounced oxidative stress in this group of acute ischemic stroke patients probably led to HDL structural changes, which could further cause an alteration or decrease of PON1 activity. Evidence of increased prooxidant level associated with decreased protective, antioxidative factors suggests their mutual involvement in this complex pathology.
氧化应激与血脂异常的关联形成了一个新出现的、参与急性缺血性卒中发生发展的动脉粥样硬化危险因素。本研究分析了氧化应激对高密度脂蛋白(HDL)颗粒结构变化的影响,这种变化与保护性对氧磷酶1(PON1)活性的改变有关。
本研究纳入了185例急性缺血性卒中患者和185例明显健康的对照者。测定了氧化应激状态、PON1状态、血脂和高敏C反应蛋白(hsCRP)。在分离出的HDL脂蛋白组分中,我们测定了氧化应激的选定标志物(丙二醛,MDA)和总巯基(SH)基团的含量。评估了氧化和PON1状态参数根据生存状态区分患者的能力。
卒中患者的HDL胆固醇水平低于对照组,PON1活性显著下降(对照组-227U/L,存活者-42U/L,致死组-61U/L,p<0.001),同时炎症更为明显。患者中存在明显的氧化应激和抗氧化保护受损。HDL组分分析显示患者的SH基团含量显著降低(对照组与患者组,p<0.05),MDA含量增加(致死组与对照组,p<0.05)。根据逻辑回归分析,疾病转归的最佳预测指标是氧化应激标志物——促氧化-抗氧化平衡(PAB)。
这组急性缺血性卒中患者中明显的氧化应激可能导致HDL结构改变,进而可能导致PON1活性改变或降低。促氧化剂水平升高与保护性抗氧化因子降低相关的证据表明它们共同参与了这一复杂的病理过程。