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Effects of Acute Stroke Serum on Non-Ischemic Cerebral and Mesenteric Vascular Function

机译:急性中风血清对非缺血性脑和肠系膜血管功能的影响

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摘要

We investigated the effects of circulating factors in serum obtained from patients in the acute phase of different subtypes of ischemic stroke on non-ischemic cerebral and mesenteric arteries, as a potential mechanism involved in influencing regional perfusion and thus clinical evolution. Posterior cerebral arteries (PCAs) and mesentery arteries (MAs) isolated from Wistar Kyoto rats were perfused with serum from acute stroke patients with large vessel disease without (LVD) or with hypertension (LVD + HTN), cardioembolism with hypertension (CE + HTN), or physiologic saline as controls. Myogenic activity and nitric oxide-dependent vasorelaxation were assessed after 2 h of intraluminal exposure to serum. Vascular function was differentially affected by sera. Exposure to LVD serum increased myogenic tone and produced endothelial dysfunction in both PCAs and MAs. However, CE + HTN serum increased tone and decreased smooth muscle sensitivity to NO in vessels from both vascular beds. LVD + HTN serum was associated with reduced smooth muscle sensitivity to NO in vessels from both vascular beds but increased tone only in PCAs. Inflammation and oxidative stress, determined by measurement of high sensitivity C-reactive protein, uric acid, and free 8-isoprostane, were enhanced in all the serum groups. These results demonstrate vasoactive properties of acute stroke serum related to stroke subtypes that could potentially contribute to the pathogenesis of early hemodynamic-based clinical events.
机译:我们调查了缺血性卒中不同亚型的急性期患者血清中循环因子对非缺血性脑和肠系膜动脉的影响,这是影响区域灌注从而影响临床发展的潜在机制。从Wistar Kyoto大鼠中分离出的后脑动脉(PCA)和肠系膜动脉(MAs)灌注无大血管疾病(LVD)或患有高血压(LVD + HTN),患有高血压的心脏栓塞(CE + HTN)的急性中风患者的血清或生理盐水作为对照。腔内暴露于血清2 h后评估肌原性活性和一氧化氮依赖性血管舒张。血清对血管功能的影响不同。暴露于LVD血清会增加PCAs和MAs的肌原性张力并产生内皮功能障碍。然而,CE + HTN血清增加了血管紧张度,降低了两张血管床血管对NO的平滑肌敏感性。 LVD + HTN血清与两张血管床中血管对NO的平滑肌敏感性降低有关,但仅在PCA中升高音调。通过测量高敏C反应蛋白,尿酸和游离的8-异前列腺素确定的炎症和氧化应激在所有血清组中均得到增强。这些结果证明了与中风亚型相关的急性中风血清的血管活性特性,可能会导致基于早期血液动力学的临床事件的发病机理。

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