缺氧性肺血管收缩:体内平衡氧传感系统的重要组成部分

IF 1.9 4区 医学 Q3 PHYSIOLOGY
Physiological research Pub Date : 2024-11-29
S L Archer, K J Dunham-Snary, Ret Bentley, E Alizadeh, E K Weir
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引用次数: 0

摘要

缺氧性肺血管收缩(HPV)可快速、可逆地匹配肺通气量(V)和灌注量(Q),优化氧气吸收和全身供氧。HPV 发生在肺小动脉 (PA),它们在缺氧时会发生独特的收缩。虽然 HPV 受内皮调节,但 HPV 的核心机制在于肺动脉平滑肌细胞(PASMC)。PASMC 线粒体氧传感器位于电子传递链(ETC)中,包括 ETC 复合物 I 中的 NDUFS2。PASMC 线粒体对缺氧的反应是根据肺泡氧张力的比例改变活性氧(ROS)和过氧化氢的产生。缺氧性 ROS 抑制会导致还原状态,从而引发氧化还原介导的对氧敏感的电压门控钾通道(包括 Kv1.5 和 Kv2.1)抑制。Kv 通道抑制会使 PASMC 去极化,打开大电导钙通道(CaL),使细胞膜钙升高并激活收缩装置。HPV 在传感器(缺氧反应线粒体)和效应器(氧敏感 K+ 通道)丰富的小 PA 中最强。出生时的吸氧会逆转胎儿的 HPV,导致新生儿肺血管阻力(PVR)迅速下降。在动脉导管(DA)中也存在类似的线粒体-心房-K+通道传感器-效应器机制,但在DASMC中,是氧诱导的线粒体ROS增加抑制了DASMC K+通道,导致DA收缩。肺不张和肺炎会引起 HPV,从而优化 V/Q 匹配,增加全身氧合。虽然单个肺叶局部缺氧时产生的 HPV 不会增加 PA 压力,但高原或睡眠呼吸暂停时出现的整体气道缺氧会导致肺动脉高压。HPV 可被药物(包括钙通道阻滞剂)抑制,或在肺部手术的单肺麻醉中用于保持术野干燥。HPV 通常不会导致肺水肿,但过量的异源 HPV 会导致高海拔肺水肿。在 COVID-19 肺炎中,SARS-CoV-2 线粒体病变抑制了 HPV。HPV是机体平衡氧传感系统的一个组成部分。关键词动脉导管 氧化还原 NDUFS2 氧敏感钾 通道 高海拔肺水肿 线粒体电子传递链 COVID-19肺炎 肺不张
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxic Pulmonary Vasoconstriction: An Important Component of the Homeostatic Oxygen Sensing System.

Hypoxic pulmonary vasoconstriction (HPV) rapidly and reversibly matches lung ventilation (V) and perfusion (Q), optimizing oxygen uptake and systemic oxygen delivery. HPV occurs in small pulmonary arteries (PA), which uniquely constrict to hypoxia. Although HPV is modulated by the endothelium the core mechanism of HPV resides in PA smooth muscle cells (PASMC). The PASMC's mitochondrial oxygen sensor lies within the electron transport chain (ETC) and includes NDUFS2 in ETC Complex-I. PASMC mitochondria respond to hypoxia by varying production of reactive oxygen species (ROS) and hydrogen peroxide in proportion to alveolar oxygen tension. Hypoxic ROS inhibition results in a state of reduction which triggers a redox-mediated inhibition of oxygen-sensitive, voltage-gated, potassium channels, including Kv1.5 and Kv2.1. Kv channel inhibition depolarizes the PASMC, opening of large-conductance calcium channels (CaL), elevating cytosolic calcium and activating the contractile apparatus. HPV is strongest in small PAs where sensors (hypoxia-responsive mitochondria) and effectors (oxygen-sensitive K+ channels) are enriched. Oxygenation at birth reverses fetal HPV, contributing to the rapid neonatal drop in pulmonary vascular resistance (PVR). A similar mitochon-drial-K+ channel sensor-effector mechanism exists in the ductus arteriosus (DA), however in DASMC it is oxygen-induced increases in mitochondrial ROS that inhibit DASMC K+ channels, causing DA constriction. Atelectasis and pneumonia elicit HPV, which optimises V/Q matching, increasing systemic oxygenation. Whilst HPV in response to localized hypoxia in a single lung lobe does not increase PA pressure; global airway hypoxia, as occurs with altitude or sleep apnea, causes pulmonary hypertension. HPV can be inhibited by drugs, including calcium channel blockers, or used to maintain a dry operative field during single lung anesthesia for lung surgery. HPV does not normally cause lung edema but excessive, heterogenous HPV contributes to high altitude pulmonary edema. HPV is suppressed in COVID-19 pneumonia by a SARS-CoV-2 mitochondriopathy. HPV is a component of the body's homeostatic oxygen sensing system. Keywords: Ductus arteriosus, Redox, NDUFS2, Oxygen sensitive potassium, Channels, High altitude pulmonary edema (HAPE), Mitochondrial electron transport chain, COVID-19 pneumonia, Atelectasis.

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来源期刊
Physiological research
Physiological research 医学-生理学
CiteScore
4.00
自引率
4.80%
发文量
108
审稿时长
3 months
期刊介绍: Physiological Research is a peer reviewed Open Access journal that publishes articles on normal and pathological physiology, biochemistry, biophysics, and pharmacology. Authors can submit original, previously unpublished research articles, review articles, rapid or short communications. Instructions for Authors - Respect the instructions carefully when submitting your manuscript. Submitted manuscripts or revised manuscripts that do not follow these Instructions will not be included into the peer-review process. The articles are available in full versions as pdf files beginning with volume 40, 1991. The journal publishes the online Ahead of Print /Pre-Press version of the articles that are searchable in Medline and can be cited.
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