Cerebrovascular effects of endothelin-1 investigated using high-resolution magnetic resonance imaging in healthy volunteers

A. Hougaard, Samaira Younis, Afrim Iljazi, K. Haanes, U. Lindberg, Mark B. Vestergaard, F. Amin, K. Sugimoto, L. Kruse, C. Ayata, M. Ashina
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引用次数: 12

Abstract

Endothelin-1 (ET-1) is a highly potent vasoconstrictor peptide released from vascular endothelium. ET-1 plays a major role in cerebrovascular disorders and likely worsens the outcome of acute ischaemic stroke and aneurismal subarachnoid haemorrhage through vasoconstriction and cerebral blood flow (CBF) reduction. Disorders that increase the risk of stroke, including hypertension, diabetes mellitus, and acute myocardial infarction, are associated with increased plasma levels of ET-1. The in vivo human cerebrovascular effects of systemic ET-1 infusion have not previously been investigated. In a two-way crossover, randomized, double-blind design, we used advanced 3 tesla MRI methods to investigate the effects of high-dose intravenous ET-1 on intra- and extracranial artery circumferences, global and regional CBF, and cerebral metabolic rate of oxygen (CMRO2) in 14 healthy volunteers. Following ET-1 infusion, we observed a 14% increase of mean arterial blood pressure, a 5% decrease of middle cerebral artery (MCA) circumference, but no effects on extracerebral arteries and no effects on CBF or CMRO2. Collectively, the findings indicate MCA constriction secondarily to blood pressure increase and not due to a direct vasoconstrictor effect of ET-1. We suggest that, as opposed to ET-1 in the subarachnoid space, intravascular ET-1 does not exert direct cerebrovascular effects in humans.
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利用高分辨率磁共振成像技术研究内皮素-1对健康志愿者脑血管的影响
内皮素-1 (ET-1)是一种从血管内皮中释放的高效血管收缩肽。ET-1在脑血管疾病中发挥重要作用,并可能通过血管收缩和脑血流量(CBF)减少而恶化急性缺血性卒中和动脉瘤性蛛网膜下腔出血的结局。高血压、糖尿病和急性心肌梗死等增加中风风险的疾病与血浆ET-1水平升高有关。全身ET-1输注对人体内脑血管的影响尚未被研究过。在双向交叉、随机、双盲设计中,我们使用先进的3特斯拉MRI方法研究了高剂量静脉注射ET-1对14名健康志愿者颅内内外动脉周长、整体和局部CBF以及脑氧代谢率(cro2)的影响。ET-1输注后,我们观察到平均动脉血压升高14%,大脑中动脉(MCA)周长降低5%,但对脑外动脉没有影响,对CBF或cmor2没有影响。总的来说,这些发现表明MCA收缩继发于血压升高,而不是由于ET-1的直接血管收缩作用。我们认为,与ET-1在蛛网膜下腔的作用相反,血管内ET-1对人类的脑血管没有直接作用。
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