Selective alpha 1-adrenergic blockade attenuates resting beat-to-beat blood pressure variability in healthy young men

IF 5.3 2区 医学 Q1 PHYSIOLOGY Physiology Pub Date : 2023-05-01 DOI:10.1152/physiol.2023.38.s1.5732317
L. Vianna, Gustavo Rodrigues, M. Daher, A. Teixeira, Igor Fernandes
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Abstract

Resting beat-to-beat blood pressure variability is a powerful predictor of cardiovascular events and end-organ damage. However, its underlying mechanisms remain incompletely understood. For instance, alterations in beat-to-beat blood pressure variability are thought to be driven by changes in both the reflex control of the autonomic nervous system and peripheral vascular function. To determine the role of peripheral sympathetic vasoconstriction on the beat-to-beat blood pressure variability, beat-to-beat heart rate (HR, by electrocardiography) and blood pressure (finger photoplethysmography) were continuously measured in seven healthy men (22 ± 5 yr) at rest (supine position), with and without (Control) a systemic and selective blockade of alpha 1-adrenergic receptors through the oral administration of Prazosin (1 mg/20 kg of body weight). Stroke volume was estimated from the blood pressure waveform (ModelFlow), permitting the calculation of cardiac output and total peripheral resistance. Two hours post-Prazosin ingestion, blood pressure responses to intravenous bolus infusion of phenylephrine were robustly reduced (-80 ± 15%, P = 0.001), indicating a significant functional blockade of alpha 1-adrenergic receptors. However, all resting hemodynamic variables were unchanged after the oral ingestion of Prazosin. Compared with control, Prazosin significantly reduced the standard deviation of systolic (5.5 ± 0.9 vs. 3.7 ± 0.7 mmHg, P = 0.004), diastolic (3.3 ± 1.0 vs. 2.4 ± 0.6 mmHg, P = 0.05), and mean blood pressure (3.7 ± 0.8 vs. 2.5 ± 0.5 mmHg, P = 0.02), as well as cardiac output (652 ± 251 vs. 428 ± 78 mL/min, P = 0.02) and total peripheral resistance (1.1 ± 0.6 vs. 0.5 ± 0.4 mmHg/L/min, P = 0.03). Similar results were found using different indices of blood pressure variability. Altogether, these findings suggest that peripheral sympathetic vasoconstriction plays a pivotal role in modulating resting beat-to-beat blood pressure variability in healthy young men. National Council for Scientific and Technological Development (CNPq; grant: 307293/2019-0 and 431740/2018-6). This is the full abstract presented at the American Physiology Summit 2023 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.
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选择性α 1-肾上腺素能阻断可减弱健康年轻男性静息搏动血压变异性
静息搏动血压变异性是心血管事件和终末器官损伤的有力预测因子。然而,其潜在机制仍不完全清楚。例如,搏动间血压变异性的改变被认为是由自主神经系统的反射控制和周围血管功能的变化驱动的。为了确定外周交感血管收缩对搏动血压变异性的作用,连续测量了7名健康男性(22±5岁)静息时(仰卧位)的搏动心率(HR)和血压(手指光体积脉搏图),并通过口服哌唑嗪(1 mg/ 20kg体重)系统性和选择性地阻断α - 1-肾上腺素能受体(对照)。从血压波形(ModelFlow)估计脑卒中容量,从而计算心输出量和总外周阻力。服用prazosin 2小时后,静脉滴注苯肾上腺素的血压反应明显降低(-80±15%,P = 0.001),表明α 1-肾上腺素能受体的功能明显阻断。然而,口服哌唑嗪后,所有静息血流动力学变量均未改变。与对照组相比,Prazosin显著降低了收缩压(5.5±0.9 vs 3.7±0.7 mmHg, P = 0.004)、舒张压(3.3±1.0 vs 2.4±0.6 mmHg, P = 0.05)、平均血压(3.7±0.8 vs 2.5±0.5 mmHg, P = 0.02)、心输出量(652±251 vs 428±78 mL/min, P = 0.02)和总外周阻力(1.1±0.6 vs 0.5±0.4 mmHg/L/min, P = 0.03)的标准差。使用不同的血压变异性指数也发现了类似的结果。综上所述,这些发现表明,外周交感血管收缩在调节健康年轻男性静息搏动血压变异性方面起着关键作用。国家科学技术发展委员会;资助:307293/2019-0和431740/2018-6)。这是在2023年美国生理学峰会上发表的完整摘要,仅以HTML格式提供。此摘要没有附加版本或附加内容。生理学没有参与同行评议过程。
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来源期刊
Physiology
Physiology 医学-生理学
CiteScore
14.50
自引率
0.00%
发文量
37
期刊介绍: Physiology journal features meticulously crafted review articles penned by esteemed leaders in their respective fields. These articles undergo rigorous peer review and showcase the forefront of cutting-edge advances across various domains of physiology. Our Editorial Board, comprised of distinguished leaders in the broad spectrum of physiology, convenes annually to deliberate and recommend pioneering topics for review articles, as well as select the most suitable scientists to author these articles. Join us in exploring the forefront of physiological research and innovation.
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