β-肾上腺素能受体阻滞可增强健康年轻人缺氧时交感神经介导的血管收缩能力

IF 5.3 2区 医学 Q1 PHYSIOLOGY Physiology Pub Date : 2024-05-01 DOI:10.1152/physiol.2024.39.s1.1213
Dain W Jacob, Brian Shariff, Braden Bond, Natasha Boyes, Jennifer L Harper, Brian Bostick, Jacqueline Limberg
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引用次数: 0

摘要

目的:血管张力受血管舒张和血管收缩影响的净平衡决定。缺氧时,全身交感神经血管收缩活动增加,但外周血管扩张占主导地位--这表明在健康状态下,血管扩张因素超过了交感神经介导的血管收缩影响因素。鉴于血管β肾上腺素能受体有助于缺氧性血管舒张,我们假设药物阻断β肾上腺素能受体将增强缺氧时血管对急性交感激活的收缩反应。研究方法13 名年轻健康的参与者(5F/8M,27±7 岁,25±3 kg/m2)完成了两次研究访问,随机并盲法口服安慰剂或普萘洛尔(1mg/kg,NCT05256069)。每次就诊时,参与者都要完成两项试验:1)10 分钟常氧(0.21 FiO2,98±0% SpO2),然后通过 2 分钟常氧冷加压试验(CPT)激活交感神经;2)5 分钟稳态缺氧(0.10±0.01 FiO2,81±1% SpO2),然后进行 2 分钟缺氧 CPT。评估前臂血流量(FBF,静脉闭塞血压计)和血压(BP,手指光电血压计)。前臂血流根据平均血压进行归一化处理(前臂血管传导,FVC)。计算 FVC 从稳态到 CPT 最后 1 分钟的变化(ΔFVC = CPT - 稳态),并以变化百分比表示(%FVC = ΔFVC/ 稳态 x 100)。结果在安慰剂条件下,血管对交感神经激活(CPT)的反应不受缺氧影响(常氧:-34±21%;缺氧:-29±32%,P=0.33)。相反,口服普萘洛尔阻断β肾上腺素能后,缺氧时交感神经介导的血管收缩增强(正常缺氧:-29±30%;缺氧:-40±27%,P=0.04)。结论:在男女混合组群中,β肾上腺素能受体阻断可增强缺氧时急性交感神经激活的血管收缩反应。这些初步数据表明,功能性β肾上腺素能受体是抑制缺氧时交感神经介导的血管收缩所必需的。基于支持肾上腺素能控制血管张力的性别差异的数据,未来的工作将寻求按性别对结果进行分层。资助:AHA 909014 (DWJ)、APS-SURF (BJB)、HL153523 (JKL)。本文是在 2024 年美国生理学峰会上发表的摘要全文,只有 HTML 格式。本摘要没有附加版本或附加内容。生理学》未参与同行评审过程。
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β-Adrenergic Receptor Blockade Augments Sympathetically Mediated Vasoconstriction during Hypoxia in Healthy Young Adults
Objective: Vascular tone is dictated by the net balance of vasodilatory and vasoconstrictor influences. During hypoxia, systemic sympathetic vasoconstrictor activity is increased but peripheral vasodilation prevails — suggesting vasodilatory factors outweigh sympathetically-mediated vasoconstrictor influences in the healthy state. Given vascular β-adrenergic receptors contribute to hypoxic vasodilation, we hypothesized pharmacological blockade of β-adrenergic receptors would augment the vasoconstrictor response to acute sympathetic activation during hypoxia. Methods: Thirteen young healthy participants (5F/8M, 27±7 yr, 25±3 kg/m2) completed two study visits randomized and blinded to oral placebo or propranolol (1mg/kg, NCT05256069). On each visit, participants completed two trials: 1) 10-min normoxia (0.21 FiO2, 98±0% SpO2) followed by sympathetic activation via a 2-min normoxic cold pressor test (CPT); 2) 5-min steady-state hypoxia (0.10±0.01 FiO2, 81±1% SpO2) followed by a 2-min hypoxic CPT. Forearm blood flow (FBF, venous occlusion plethysmography) and blood pressure (BP, finger photoplethysmography) were assessed. FBF was normalized for mean BP (forearm vascular conductance, FVC). A change in FVC from steady-state to the last 1-min of CPT was calculated (ΔFVC = CPT − steady-state) and expressed as a percent change (%FVC = ΔFVC/steady-state x 100). Results: The vascular response to sympathetic activation (CPT) was unaffected by hypoxia under placebo conditions (normoxia: -34±21%; hypoxia: -29±32%, p=0.33). In contrast, following β-adrenergic blockade with oral propranolol, sympathetically-mediated vasoconstriction was augmented during hypoxia (normoxia: -29±30%; hypoxia: -40±27%, p=0.04). Conclusion: β-adrenergic receptor blockade augments the vasoconstrictor response to acute sympathetic activation during hypoxia in a mixed-sex cohort. These preliminary data indicate functional β-adrenergic receptors are required to restrain sympathetically-mediated vasoconstriction during hypoxia. Based on data supporting sex-related differences in adrenergic control of vascular tone, future work will seek to stratify results by sex. Funding: AHA 909014 (DWJ), APS-SURF (BJB), HL153523 (JKL). This is the full abstract presented at the American Physiology Summit 2024 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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Physiology
Physiology 医学-生理学
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