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Endothelial damage in major depression patients is modulated by SSRI treatment, as demonstrated by circulating biomarkers and an in vitro cell model

机译:重症抑郁症患者的内皮损伤通过SSRI治疗得到调节,循环生物标志物和体外细胞模型证明了这一点

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There is a link between depression, cardiovascular events and inflammation. We have explored this connection through endothelial dysfunction, using in vivo and in vitro approaches. We evaluated circulating biomarkers of endothelial dysfunction in patients with major depression at their diagnosis (MD-0) and during antidepressant treatment with the selective serotonin reuptake inhibitor escitalopram, for 8 and 24 weeks (MD-8 and MD-24). Results were always compared with matched healthy controls (CON). We measured in vivo circulating endothelial cells (CECs) and endothelial progenitor cells (EPCs) in blood samples, and assessed plasma levels of soluble von Willebrand factor (VWF) and vascular cell adhesion molecule-1 (VCAM-1). CEC counts, soluble VWF and VCAM-1 were statistically elevated in MD-0 ( P In vitro studies were performed in human endothelial cells cultured in the presence of sera from each study group. Elevated expression of the inflammation marker intercellular adhesion molecule-1 and oxidative stress, with lower presence of endothelial nitric oxide synthase and higher reactive oxygen species production, were found in cells exposed to MD-0 sera ( P
机译:抑郁症,心血管事件和炎症之间存在联系。我们已经使用体内和体外方法通过内皮功能障碍探索了这种联系。我们评估了患有严重抑郁症的患者在诊断时(MD-0)以及使用选择性5-羟色胺再摄取抑制剂依他普仑进行抗抑郁治疗期间的内皮功能障碍的循环生物标记,分别持续8周和24周(MD-8和MD-24)。始终将结果与匹配的健康对照(CON)进行比较。我们测量了血液样本中的体内循环内皮细胞(CEC)和内皮祖细胞(EPC),并评估了血浆可溶性可溶性血管性假血友病因子(VWF)和血管细胞粘附分子1(VCAM-1)的水平。在MD-0中,CEC计数,可溶性VWF和VCAM-1的表达均具有统计学意义的升高(P在每个研究组中在存在血清的情况下在培养的人内皮细胞中进行体外研究。在暴露于MD-0血清的细胞中发现了氧化应激,其中内皮一氧化氮合酶的含量较低,而活性氧的生成量较高(P

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