β-肾上腺素能阻滞增加肺血管阻力并导致高海拔缺氧性肺血管收缩:一项生理学研究。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS European Heart Journal - Cardiovascular Pharmacotherapy Pub Date : 2024-07-16 DOI:10.1093/ehjcvp/pvae004
Matthias Peter Hilty, Christoph Siebenmann, Peter Rasmussen, Stefanie Keiser, Andrea Müller, Carsten Lundby, Marco Maggiorini
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引用次数: 0

摘要

背景:越来越多的高血压患者在高海拔地区旅行时使用降压药(如降压药)。然而,虽然缺氧会导致肺动脉压(Ppa)和肺血管阻力(PVR)增加,但自律神经系统的作用尚不清楚。在动物身上,β-肾上腺素能阻断剂诱导了常氧状态下的肺血管收缩,并夸大了缺氧状态下的肺血管收缩(HPV),而这两种效应都被毒蕈碱阻断剂所消除。因此,我们推测普萘洛尔(PROP)会增加人体在常氧状态下的Ppa和PVR,并加剧HPV,而甘珀酸(GLYC)会消除普萘洛尔的这些作用:方法:在海平面(SL,488 米)和在海拔 3454 米(HA)逗留三周后,对七名健康男性低地人在未服药、服用 PROP 和 PROP+GLYC 的情况下进行肺动脉压力有创测量。进行了双侧大腿袖带释放操作,以得出肺压力-流量关系和肺血管扩张性:结果:在 SL,PROP 使 Ppa 和 PVR 从(平均值±标准平均值)14±1 增加到 17±1mmHg,从 69±8 增加到 108±11dyn*s*cm-5(分别增加 21% 和 57%,p=0.01 和 p结论:我们的数据显示,β-肾上腺素能阻滞增加了 PVR,而毒蕈碱能阻滞降低了 PVR,但两者都增加了肺动脉弹性。未来的研究可能会证实,β 肾上腺素能阻滞剂会增加 HPV,这一发现对使用 β 受体阻滞剂预防或治疗心血管疾病的登山者的管理具有潜在意义。
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Beta-adrenergic blockade increases pulmonary vascular resistance and causes exaggerated hypoxic pulmonary vasoconstriction at high altitude: a physiological study.

Background: An increasing number of hypertensive persons travel to high altitude (HA) while using antihypertensive medications such as beta-blockers. Nevertheless, while hypoxic exposure initiates an increase in pulmonary artery pressure (Ppa) and pulmonary vascular resistance (PVR), the contribution of the autonomic nervous system is unclear. In animals, beta-adrenergic blockade has induced pulmonary vasoconstriction in normoxia and exaggerated hypoxic pulmonary vasoconstriction (HPV) and both effects were abolished by muscarinic blockade. We thus hypothesized that in humans, propranolol (PROP) increases Ppa and PVR in normoxia and exaggerates HPV, and that these effects of PROP are abolished by glycopyrrolate (GLYC).

Methods: In seven healthy male lowlanders, Ppa was invasively measured without medication, with PROP and PROP + GLYC, both at sea level (SL, 488 m) and after a 3-week sojourn at 3454 m altitude (HA). Bilateral thigh-cuff release manoeuvres were performed to derive pulmonary pressure-flow relationships and pulmonary vessel distensibility.

Results: At SL, PROP increased Ppa and PVR from (mean ± SEM) 14 ± 1 to 17 ± 1 mmHg and from 69 ± 8 to 108 ± 11 dyn s cm-5 (21% and 57% increase, P = 0.01 and P < 0.0001). The PVR response to PROP was amplified at HA to 76% (P < 0.0001, P[interaction] = 0.05). At both altitudes, PROP + GLYC abolished the effect of PROP on Ppa and PVR. Pulmonary vessel distensibility decreased from 2.9 ± 0.5 to 1.7 ± 0.2 at HA (P < 0.0001) and to 1.2 ± 0.2 with PROP, and further decreased to 0.9 ± 0.2% mmHg-1 with PROP + GLYC (P = 0.01).

Conclusions: Our data show that beta-adrenergic blockade increases, and muscarinic blockade decreases PVR, whereas both increase pulmonary artery elastance. Future studies may confirm potential implications from the finding that beta-adrenergic blockade exaggerates HPV for the management of mountaineers using beta-blockers for prevention or treatment of cardiovascular conditions.

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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