经颅多普勒评价正常人对乙酰唑胺的脑血管反应性。

Artery Pub Date : 1993-01-01
M Mancini, S De Chiara, A Postiglione, L A Ferrara
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引用次数: 0

摘要

乙酰唑胺(Acetazolamide, AZ)是碳酸酐酶的选择性抑制剂,经静脉注射氙133技术证实可增加脑血流量(CBF)。在这项研究中,我们通过大脑中动脉(MCA)内的经颅多普勒(TCD)评估了10名正常受试者对AZ的脑血管反应性,因为有几篇报道表明脑血流速度与CBF密切相关。注射1克AZ后,所有受试者血流速度均明显增加,在给药后20分钟收缩期和舒张期血流速度均达到峰值。与基础值相比,收缩速度增加35%,舒张速度增加50%。与Xenon 133技术相比,每次调查只提供一次测量,TCD允许连续监测AZ输注后的血流动力学变化。静止时MCA舒张速度与年龄呈负相关(r = -)。804, p < 0.01);基线舒张速度与最大百分比增量呈负相关(r = -)。745 p < 0.05)。在实验条件下,血压和心率没有变化。这些结果证实了AZ试验在评估脑血管反应性方面的有效性,并强烈支持将TCD技术应用于AZ以研究正常健康受试者和有脑血管功能不全风险的患者的脑血管血流动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcranial Doppler evaluation of cerebrovascular reactivity to acetazolamide in normal subjects.

Acetazolamide (AZ), the selective inhibitor of carbonic anhydrase, was proved by intravenous Xenon 133 technique to increase cerebral blood flow (CBF). In this study cerebrovascular reactivity to AZ was evaluated in 10 normal subjects by transcranial Doppler (TCD) within the middle cerebral artery (MCA), since several reports have demonstrated that velocity of cerebral blood flow is well correlated to CBF. After 1 gr AZ injection blood flow velocity markedly increased in all subjects, with a peak in both systolic and diastolic velocity 20 min after drug administration. At that time systolic velocity increased by 35% and diastolic velocity by 50% in comparison to basal values. In contrast with Xenon 133 technique which gives one measurement only for each investigation, TCD allows a continuous monitoring of haemodynamic change following AZ infusion. MCA diastolic velocity at rest was inversely related to age (r = -.804, p < 0.01); baseline diastolic velocity was inversely related to the maximum percentage increment (r = -.745 p < .05). No change in blood pressure and heart rate was observed under experimental conditions. These results, confirm the usefulness of the AZ test in the evaluation of cerebrovascular reactivity and strongly support the use of TCD technique applied to AZ in order to investigate cerebrovascular haemodynamics in normal healthy subjects and in patients at risk of cerebrovascular insufficiency.

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