Yasunari Kenichi, Watanabe Takanori, Nakamura Munehiro
Department of Medicine and Cardiology, Graduate School of Medicine, Osaka City University, 1-4-3 Asahi-machi, Osaka 545-8585, Japan.
Curr Pharm Biotechnol. 2006 Apr;7(2):73-80. doi: 10.2174/138920106776597612.
To better identify patients at high risk for cardiovascular events, several markers of risk have been proposed for use in screening. Recently, oxidative stress and inflammation have been evaluated as potential tools for prediction of the risk of cardiovascular events. Among them, we have measured reactive oxygen species (ROS) formation by polymorphonuclear cells (PMNs) and mononuclear cells (MNCs), since they may be a possible link between inflammation and oxidative stress. ROS formation by PMNs and MNCs was measured by a gated flow cytometric assay. Such biotechnological method of measuring ROS formation by PMNs and MNCs will make it possible that we measure vascular oxidative stress and vascular inflammation at the same time from only small amount of blood. We will state in this review that ROS formation by PMNs and MNCs are regulated by different mechanisms, although PMNs and MNCs are circulating in the same blood. Moreover, we will state that ROS formation by PMNs are regulated by blood pressure, Hb A(1C) and oxidided LDL. ROS formation by MNCs are regulated by vascular inflammation, and that ROS formation by MNCs are also related to various cardiovascular risks such as LV mass, norepinephrine, IMT, and nocturnal blood pressure.
为了更好地识别心血管事件高危患者,已提出多种风险标志物用于筛查。最近,氧化应激和炎症已被评估为预测心血管事件风险的潜在工具。其中,我们测量了多形核细胞(PMN)和单核细胞(MNC)产生的活性氧(ROS),因为它们可能是炎症与氧化应激之间的一个潜在联系。通过门控流式细胞术检测PMN和MNC产生ROS的情况。这种测量PMN和MNC产生ROS的生物技术方法将使我们仅从少量血液中就能同时测量血管氧化应激和血管炎症成为可能。在本综述中,我们将指出,尽管PMN和MNC在同一份血液中循环,但它们产生ROS的情况受不同机制调控。此外,我们将指出,PMN产生ROS受血压、糖化血红蛋白(Hb A1C)和氧化型低密度脂蛋白调控。MNC产生ROS受血管炎症调控,并且MNC产生ROS还与多种心血管风险相关,如左心室质量、去甲肾上腺素、内膜中层厚度(IMT)和夜间血压。